Single nucleotide polymorphisms in genes

Description

RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No. 09/657,472, filed Sep. 7, 2000, which claims the benefit of U.S. Provisional Application Serial No. 60/153,357, filed Sep. 10, 1999, U.S. Provisional Application Serial No. 60/220,947, filed Jul. 26, 2000, and U.S. Provisional Application Serial No. 60/225,724, filed Aug. 16, 2000, the entire teachings of all of which are incorporated herein by reference.

BACKGROUND OF THE INVENTION

The genomes of all organisms undergo spontaneous mutation in the course of their continuing evolution, generating variant forms of progenitor nucleic acid sequences (Gusella, Ann. Rev. Biochem. 55, 831-854 (1986)). The variant form may confer an evolutionary advantage or disadvantage relative to a progenitor form, or may be neutral. In some instances, a variant form confers a lethal disadvantage and is not transmitted to subsequent generations of the organism. In other instances, a variant form confers an evolutionary advantage to the species and is eventually incorporated into the DNA of many or most members of the species and effectively becomes the progenitor form. In many instances, both progenitor and variant form(s) survive and co-exist in a species population. The coexistence of multiple forms of a sequence gives rise to polymorphisms.

Several different types of polymorphism have been reported. A restriction fragment length polymorphism (RFLP) is a variation in DNA sequence that alters the length of a restriction fragment (Botstein et al., Am. J. Hum. Genet. 32, 314-331 (1980)). The restriction fragment length polymorphism may create or delete a restriction site, thus changing the length of the restriction fragment. RFLPs have been widely used in human and animal genetic analyses (see WO 90/13668; W090/11369; Donis-Keller, Cell 51, 319-337 (1987); Lander et al., Genetics 121, 85-99 (1989)). When a heritable trait can be linked to a particular RFLP, the presence of the RFLP in an individual can be used to predict the likelihood that the animal will also exhibit the trait.

Other polymorphisms take the form of short tandem repeats (STRs) that include tandem di-, tri- and tetra-nucleotide repeated motifs. These tandem repeats are also referred to as variable number tandem repeat (VNTR) polymorphisms. VNTRs have been used in identity and paternity analysis (U.S. Pat. No. 5,075,217; Armour et al., FEBS Lett. 307, 113-115 (1992); Horn et al., WO 91/14003; Jeffreys, EP 370,719), and in a large number of genetic mapping studies.

Other polymorphisms take the form of single nucleotide variations between individuals of the same species. Such polymorphisms are far more frequent than RFLPs, STRs and VNTRs. Some single nucleotide polymorphisms (SNP) occur in protein-coding nucleic acid sequences (coding sequence SNP (cSNP)), in which case, one of the polymorphic forms may give rise to the expression of a defective or otherwise variant protein and, potentially, a genetic disease. Examples of genes in which polymorphisms within coding sequences give rise to genetic disease include β-globin (sickle cell anemia), apoE4 (Alzheimer's Disease), Factor V Leiden (thrombosis), and CFTR (cystic fibrosis). cSNPs can alter the codon sequence of the gene and therefore specify an alternative amino acid. Such changes are called “missense” when another amino acid is substituted, and “nonsense” when the alternative codon specifies a stop signal in protein translation. When the cSNP does not alter the amino acid specified the cSNP is called “silent”.

Other single nucleotide polymorphisms occur in noncoding regions. Some of these polymorphisms may also result in defective protein expression (e.g., as a result of defective splicing). Other single nucleotide polymorphisms have no phenotypic effects.

Single nucleotide polymorphisms can be used in the same manner as RFLPs and VNTRs, but offer several advantages. Single nucleotide polymorphisms occur with greater frequency and are spaced more uniformly throughout the genome than other forms of polymorphism. The greater frequency and uniformity of single nucleotide polymorphisms means that there is a greater probability that such a polymorphism will be found in close proximity to a genetic locus of interest than would be the case for other polymorphisms. The different forms of characterized single nucleotide polymorphisms are often easier to distinguish than other types of polymorphism (e.g., by use of assays employing allele-specific hybridization probes or primers).

Only a small percentage of the total repository of polymorphisms in humans and other organisms has been identified. The limited number of polymorphisms identified to date is due to the large amount of work required for their detection by conventional methods. For example, a conventional approach to identifying polymorphisms might be to sequence the same stretch of DNA in a population of individuals by dideoxy sequencing. In this type of approach, the amount of work increases in proportion to both the length of sequence and the number of individuals in a population and becomes impractical for large stretches of DNA or large numbers of persons.

SUMMARY OF THE INVENTION

Work described herein pertains to the identification of polymorphisms which can predispose individuals to disease, by resequencing large numbers of genes in a large number of individuals. Various genes from a number of individuals have been resequenced as described herein, and SNPs in these genes have been discovered (see the Table and FIG. 3). Some of these SNPs are cSNPs which specify a different amino acid sequence, some of the SNPs are silent cSNPs and some of these cSNPs specify a stop signal in protein translation. Some of the identified SNPs were located in non-coding regions.

The invention relates to a gene which comprises a single nucleotide polymorphism at a specific location. In a particular embodiment the invention relates to the variant allele of a gene having a single nucleotide polymorphism, which variant allele differs from a reference allele by one nucleotide at the site(s) identified in the Table and FIG. 3. Complements of these nucleic acid sequences are also included. The nucleic acid molecules can be DNA or RNA, and can be double- or single-stranded. Nucleic acid molecules can be, for example, 5-10, 5-15, 10-20, 5-25, 10-30, 10-50 or 10-100 bases long.

The invention further provides allele-specific oligonucleotides that hybridize to the reference or variant allele of a gene comprising a single nucleotide polymorphism or to the complement thereof. These oligonucleotides can be probes or primers.

The invention further provides a method of analyzing a nucleic acid from an individual. The method determines which base is present at any one of the polymorphic sites shown in the Table and/or FIG. 3. Optionally, a set of bases occupying a set of the polymorphic sites shown in the Table and/or FIG. 3 is determined. This type of analysis can be performed on a number of individuals, who are tested for the presence of a disease phenotype. The presence or absence of disease phenotype is then correlated with a base or set of bases present at the polymorphic site or sites in the individuals tested.

Thus, the invention further relates to a method of predicting the presence, absence, likelihood of the presence or absence, or severity of a particular phenotype or disorder associated with a particular genotype. The method comprises obtaining a nucleic acid sample from an individual and determining the identity of one or more bases (nucleotides) at polymorphic sites of genes described herein, wherein the presence of a particular base is correlated with a specified phenotype or disorder, thereby predicting the presence, absence, likelihood of the presence or absence, or severity of the phenotype or disorder in the individual.

The thrombospondins are a family of extracellular matrix (ECM) glycoproteins that modulate many cell behaviors including adhesion, migration, and proliferation. Thrombospondins (also known as thrombin sensitive proteins or TSPs) are large molecular weight glycoproteins composed of three identical disulfide-linked polypeptide chains. The results described herein also reveal an important association between alterations, particularly SNPs, in TSP genes, particularly TSP-1 and TSP-4, and vascular disease. In particular, SNPs in these genes which are associated with premature coronary artery disease (CAD)(or coronary heart disease) and myocardial infarction (MI) have been identified and represent a potentially vital marker of upstream biology influencing the complex process of atherosclerotic plaque generation and vulnerability.

Thus, the invention relates to the TSP gene SNPs identified as described herein, both singly and in combination, as well as to the use of these SNPs, and others in TSP genes, particularly those nearby in linkage disequilibrium with these SNPs, for diagnosis, prediction of clinical course and treatment response for vascular disease, development of new treatments for vascular disease based upon comparison of the variant and normal versions of the gene or gene product, and development of cell-culture based and animal models for research and treatment of vascular disease. The invention further relates to novel compounds and pharmaceutical compositions for use in the diagnosis and treatment of such disorders. In preferred embodiments, the vascular disease is CAD or MI.

The invention relates to isolated nucleic acid molecules comprising all or a portion of the variant allele of TSP-1 (e.g., as exemplified by SEQ ID NO: 1), and to isolated nucleic acid molecules comprising all or a portion of the variant allele of TSP-4 (e.g., as exemplified by SEQ ID NO: 3). Preferred portions are at least 10 contiguous nucleotides and comprise the polymorphic site, e.g., a portion of SEQ ID NO: 1 which is at least 10 contiguous nucleotides and comprises the “G” at position 2210, or a portion of SEQ ID NO: 3 which is at least 10 contiguous nucleotides and comprises the “C” at position 1186. The invention further relates to isolated gene products, e.g., polypeptides or proteins, which are encoded by a nucleic acid molecule comprising all or a portion of the variant allele of TSP-1 or TSP-4 (e.g., SEQ ID NO: 1 or SEQ ID NO: 3, respectively). The invention also relates to nucleic acid molecules which hybridize to and/or share identity with the variant alleles identified herein (or their complements) and which also comprise the variant nucleotide at the SNP site.

The invention further relates to isolated proteins or polypeptides comprising all or a portion of the variant amino acid sequence of TSP-1 (e.g., as exemplified by SEQ ID NO: 2), and to isolated proteins or polypeptides comprising all or a portion of the variant amino acid sequence of TSP-4 (e.g., as exemplified by SEQ ID NO: 4). Preferred polypeptides are at least 10 contiguous amino acids and comprise the polymorphic amino acid, e.g., a portion of SEQ ID NO: 2 which is at least 10 contiguous amino acids and comprises the serine at residue 700, or a portion of SEQ ID NO: 4 which is at least 10 contiguous amino acids and comprises the proline at residue 387. The invention further relates to isolated nucleic acid molecules encoding such proteins and polypeptides, as well as to antibodies which bind, e.g., specifically, to such proteins and polypeptides.

The invention further relates to a method of diagnosing or aiding in the diagnosis of a disorder associated with the presence of one or more of (a) a G at nucleotide position 2210 of SEQ ID NO: 1; or (b) a C at nucleotide position 1186 of SEQ ID NO: 3 in an individual. The method comprises obtaining a nucleic acid sample from the individual and determining the nucleotide present at one or more of the indicated nucleotide positions, wherein presence of one or more of (a) a G at nucleotide position 2210 of SEQ ID NO: 1; or (b) a C at nucleotide position 1186 of SEQ ID NO: 3 is indicative of increased likelihood of said disorder in the individual as compared with an appropriate control, e.g., an individual having the reference nucleotide at one or more of said positions. In a particular embodiment the disorder is a vascular disease selected from the group consisting of atherosclerosis, coronary heart or artery disease, MI, stroke, peripheral vascular diseases, venous thromboembolism and pulmonary embolism. In a preferred embodiment, the vascular disease is selected from the group consisting of CAD and MI.

The invention further relates to a method of diagnosing or aiding in the diagnosis of a disorder associated with one or more of (a) a G at nucleotide position 2210 of SEQ ID NO: 1; or (b) a C at nucleotide position 1186 of SEQ ID NO: 3 in an individual. The method comprises obtaining a nucleic acid sample from the individual and determining the nucleotide present at one or more of the indicated nucleotide positions, wherein presence of one or more of (a) an A at nucleotide position 2210 of SEQ ID NO: 1; or (b) a G at nucleotide position 1186 of SEQ ID NO: 3 is indicative of decreased likelihood of said disorder in the individual as compared with an appropriate control, e.g., an individual having the variant nucleotide at said position. In a particular embodiment the disorder is a vascular disease selected from the group consisting of atherosclerosis, coronary heart or artery disease, MI, stroke, peripheral vascular diseases, venous thromboembolism and pulmonary embolism. In a preferred embodiment, the vascular disease is selected from the group consisting of CAD and MI.

In one embodiment, the invention relates to a method for predicting the likelihood that an individual will have a vascular disease (or aiding in the diagnosis of a vascular disease), comprising the steps of obtaining a DNA sample from an individual to be assessed and determining the nucleotide present at one or more of nucleotide positions 2210 of SEQ ID NO: 1 or 1186 of SEQ ID NO: 3. The presence of the reference nucleotide at one or more of these positions indicates that the individual has a lower likelihood of having a vascular disease than an individual having the variant nucleotide at one or more of these positions, or a lower likelihood of having severe symptomology. In a particular embodiment, the individual is an individual at risk for development of a vascular disease.

The invention further relates to a method of diagnosing or aiding in the diagnosis of a disorder associated with the presence of one or more of (a) a serine at amino acid position 700 of SEQ ID NO: 2; or (b) a proline at amino acid position 387 of SEQ ID NO: 4 in an individual. The method comprises obtaining a biological sample containing the TSP-1 and/or TSP-4 protein or relevant portion thereof from the individual and determining the amino acid present at one or more of the indicated amino acid positions, wherein presence of one or more of (a) a serine at amino acid position 700 of SEQ ID NO: 2; or (b) a proline at amino acid position 387 of SEQ ID NO: 4 is indicative of increased likelihood of said disorder in the individual as compared with an appropriate control, e.g., an individual having the reference amino acid at one or more of said positions.

The invention further relates to a method of diagnosing or aiding in the diagnosis of a disorder associated with one or more of (a) a serine at amino acid position 700 of SEQ ID NO: 2; or (b) a proline at amino acid position 387 of SEQ ID NO: 4 in an individual. The method comprises obtaining a biological sample containing the TSP-1 and/or TSP-4 protein or relevant portion thereof from the individual and determining the amino acid present at one or more of the indicated amino acid positions, wherein presence of one or more of (a) an asparagine at amino acid position 700 of SEQ ID NO: 2; or (b) an alanine at amino acid position 387 of SEQ ID NO: 4 is indicative of decreased likelihood of said disorder in the individual as compared with an appropriate control, e.g., an individual having the variant amino acid at one or more of said positions.

In one embodiment, the invention relates to a method for predicting the likelihood that an individual will have a vascular disease (or aiding in the diagnosis of a vascular disease), comprising the steps of obtaining a biological sample comprising the TSP-1 and/or TSP-4 protein or relevant portion thereof from an individual to be assessed and determining the amino acid present at one or more of amino acid positions 700 of SEQ ID NO: 2 or 387 of SEQ ID NO: 4. The presence of the reference amino acid at one or more of these positions indicates that the individual has a lower likelihood of having a vascular disease than an individual having the variant amino acid at one or more of these positions, or a lower likelihood of having severe symptomology. In a particular embodiment, the individual is an individual at risk for development of a vascular disease.

In another embodiment, the invention relates to pharmaceutical compositions comprising a reference TSP-1 and/or TSP-4 gene or gene product, or active portion thereof, for use in the treatment of vascular diseases. The invention further relates to the use of agonists and antagonists of TSP-1 and TSP-4 activity for use in the treatment of vascular diseases. In a particular embodiment the vascular disease is selected from the group consisting of atherosclerosis, coronary heart or artery disease, MI, stroke, peripheral vascular diseases, venous thromboembolism and pulmonary embolism. In a preferred embodiment, the vascular disease is selected from the group consisting of CAD and MI.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A-1D show the reference nucleotide (SEQ ID NO: 1) and amino acid (SEQ ID NO: 2) sequences for TSP-1.

FIGS. 2A-2C show the reference nucleotide (SEQ ID NO: 3) and amino acid (SEQ ID NO: 4) sequences for TSP-4.

FIG. 3 shows a table providing detailed information about the SNPs identified herein. Column one shows the internal polymorphism identifier. Column two shows the accession number for the reference sequence in the TIGR database which can be found on the world wide web at tigr.org/tdb/hgi/searching/hgigreports.html. Column three shows the nucleotide position for the SNP site. Column four shows the gene in which the polymorphism was identified. Column five shows the polymorphic site and additional flanking sequence on each side of the polymorphism. Column six shows the type of mutation produced by the polymorphism. Columns seven and eight show the reference and alternate (variant) nucleotides, respectively, for the SNP. Columns nine and ten show the reference and alternate (variant) amino acids, respectively, encoded by the alleles of the gene.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to a gene which comprises a single nucleotide polymorphism (SNP) at a specific location. The gene which includes the SNP has at least two alleles, referred to herein as the reference allele and the variant allele. The reference allele (prototypical or wild type allele) has been designated arbitrarily and typically corresponds to the nucleotide sequence of the gene which has been deposited with GenBank or TIGR under a given Accession number. The variant allele differs from the reference allele by one nucleotide at the site(s) identified in the Table. The present invention also relates to variant alleles of the described genes and to complements of the variant alleles. The invention also relates to nucleic acid molecules which hybridize to and/or share identity with the variant alleles identified herein (or their complements) and which also comprise the variant nucleotide at the SNP site.

The invention further relates to portions of the variant alleles and portions of complements of the variant alleles which comprise (encompass) the site of the SNP and are at least 5 nucleotides in length. Portions can be, for example, 5-10, 5-15, 10-20, 5-25, 10-30, 10-50 or 10-100 bases long. For example, a portion of a variant allele which is 21 nucleotides in length includes the single nucleotide polymorphism (the nucleotide which differs from the reference allele at that site) and twenty additional nucleotides which flank the site in the variant allele. These nucleotides can be on one or both sides of the polymorphism. Polymorphisms which are the subject of this invention are defined in the Table with respect to the reference sequence deposited in GenBank or TIGR under the Accession number indicated. For example, the invention relates to a portion of a gene (e.g., AT3) having a nucleotide sequence as deposited in GenBank (e.g., U11270) comprising a single nucleotide polymorphism at a specific position (e.g., nucleotide 11918). The reference nucleotide for AT3 is shown in column 8, and the variant nucleotide is shown in column 9 of the Table. The nucleotide sequences of the invention can be double- or single-stranded.

The invention further provides allele-specific oligonucleotides that hybridize to the reference or variant allele of a gene comprising a single nucleotide polymorphism or to the complement thereof. These oligonucleotides can be probes or primers.

The invention further provides a method of analyzing a nucleic acid from an individual. The method determines which base is present at any one of the polymorphic sites shown in the Table and/or FIG. 3. Optionally, a set of bases occupying a set of the polymorphic sites shown in the Table and/or FIG. 3 is determined. This type of analysis can be performed on a number of individuals, who are tested for the presence of a disease phenotype. The presence or absence of disease phenotype is then correlated with a base or set of bases present at the polymorphic site or sites in the individuals tested.

Thus, the invention further relates to a method of predicting the presence, absence, likelihood of the presence or absence, or severity of a particular phenotype or disorder associated with a particular genotype. The method comprises obtaining a nucleic acid sample from an individual and determining the identity of one or more bases (nucleotides) at polymorphic sites of genes described herein, wherein the presence of a particular base is correlated with a specified phenotype or disorder, thereby predicting the presence, absence, likelihood of the presence or absence, or severity of the phenotype or disorder in the individual.

Definitions

A nucleic acid molecule or oligonucleotide can be DNA or RNA, and single- or double-stranded. Nucleic acid molecules and oligonucleotides can be naturally occurring or synthetic, but are typically prepared by synthetic means. Preferred nucleic acid molecules and oligonucleotides of the invention include segments of DNA, or their complements, which include any one of the polymorphic sites shown in the Table. The segments can be between 5 and 250 bases, and, in specific embodiments, are between 5-10, 5-20, 10-20, 10-50, 20-50 or 10-100 bases. For example, the segment can be 21 bases. The polymorphic site can occur within any position of the segment. The segments can be from any of the allelic forms of DNA shown in the Table.

As used herein, the terms “nucleotide”, “base” and “nucleic acid” are intended to be equivalent. The terms “nucleotide sequence”, “nucleic acid sequence”, “nucleic acid molecule” and “segment” are intended to be equivalent.

Hybridization probes are oligonucleotides which bind in a base-specific manner to a complementary strand of nucleic acid. Such probes include peptide nucleic acids, as described in Nielsen et al., Science 254, 1497-1500 (1991). Probes can be any length suitable for specific hybridization to the target nucleic acid sequence. The most appropriate length of the probe may vary depending upon the hybridization method in which it is being used; for example, particular lengths may be more appropriate for use in microfabricated arrays, while other lengths may be more suitable for use in classical hybridization methods. Such optimizations are known to the skilled artisan. Suitable probes and primers can range from about 5 nucleotides to about 30 nucleotides in length. For example, probes and primers can be 5, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 25, 26, 28 or 30 nucleotides in length. The probe or primer preferably overlaps at least one polymorphic site occupied by any of the possible variant nucleotides. The nucleotide sequence can correspond to the coding sequence of the allele or to the complement of the coding sequence of the allele.

As used herein, the term “primer” refers to a single-stranded oligonucleotide which acts as a point of initiation of template-directed DNA synthesis under appropriate conditions (e.g., in the presence of four different nucleoside triphosphates and an agent for polymerization, such as DNA or RNA polymerase or reverse transcriptase) in an appropriate buffer and at a suitable temperature. The appropriate length of a primer depends on the intended use of the primer, but typically ranges from 15 to 30 nucleotides. Short primer molecules generally require cooler temperatures to form sufficiently stable hybrid complexes with the template. A primer need not reflect the exact sequence of the template, but must be sufficiently complementary to hybridize with a template. The term primer site refers to the area of the target DNA to which a primer hybridizes. The term primer pair refers to a set of primers including a 5′ (upstream) primer that hybridizes with the 5′ end of the DNA sequence to be amplified and a 3′ (downstream) primer that hybridizes with the complement of the 3′ end of the sequence to be amplified.

As used herein, linkage describes the tendency of genes, alleles, loci or genetic markers to be inherited together as a result of their location on the same chromosome. It can be measured by percent recombination between the two genes, alleles, loci or genetic markers.

As used herein, polymorphism refers to the occurrence of two or more genetically determined alternative sequences or alleles in a population. A polymorphic marker or site is the locus at which divergence occurs. Preferred markers have at least two alleles, each occurring at frequency of greater than 1%, and more preferably greater than 10% or 20% of a selected population. A polymorphic locus may be as small as one base pair. Polymorphic markers include restriction fragment length polymorphisms, variable number of tandem repeats (VNTR's), hypervariable regions, minisatellites, dinucleotide repeats, trinucleotide repeats, tetranucleotide repeats, simple sequence repeats, and insertion elements such as Alu. The first identified allelic form is arbitrarily designated as the reference form and other allelic forms are designated as alternative or variant alleles. The allelic form occurring most frequently in a selected population is sometimes referred to as the wildtype form. Diploid organisms may be homozygous or heterozygous for allelic forms. A diallelic or biallelic polymorphism has two forms. A triallelic polymorphism has three forms.

Work described herein pertains to the resequencing of large numbers of genes in a large number of individuals to identify polymorphisms which can predispose individuals to disease. For example, polymorphisms in genes which are expressed in liver may predispose individuals to disorders of the liver. By altering amino acid sequence, SNPs may alter the function of the encoded proteins. The discovery of the SNP facilitates biochemical analysis of the variants and the development of assays to characterize the variants and to screen for pharmaceutical that would interact directly with on or another form of the protein. SNPs (including silent SNPs) also enable the development of specific DNA, RNA, or protein-based diagnostics that detect the presence or absence of the polymorphism in particular conditions.

A single nucleotide polymorphism occurs at a polymorphic site occupied by a single nucleotide, which is the site of variation between allelic sequences. The site is usually preceded by and followed by highly conserved sequences of the allele (e.g., sequences that vary in less than 1/100 or 1/1000 members of the populations).

A single nucleotide polymorphism usually arises due to substitution of one nucleotide for another at the polymorphic site. A transition is the replacement of one purine by another purine or one pyrimidine by another pyrimidine. A transversion is the replacement of a purine by a pyrimidine or vice versa. Single nucleotide polymorphisms can also arise from a deletion of a nucleotide or an insertion of a nucleotide relative to a reference allele. Typically the polymorphic site is occupied by a base other than the reference base. For example, where the reference allele contains the base “T” at the polymorphic site, the altered allele can contain a “C”, “G” or “A” at the polymorphic site.

The invention also relates to nucleic acid molecules which hybridize to the variant alleles identified herein (or their complements) and which also comprise the variant nucleotide at the SNP site. Hybridizations are usually performed under stringent conditions, for example, at a salt concentration of no more than 1 M and a temperature of at least 25° C. For example, conditions of 5×SSPE (750 mM NaCl, 50 mM NaPhosphate, 5 mM EDTA, pH 7.4) and a temperature of 25-30° C., or equivalent conditions, are suitable for allele-specific probe hybridizations. Equivalent conditions can be determined by varying one or more of the parameters given as an example, as known in the art, while maintaining a similar degree of identity or similarity between the target nucleotide sequence and the primer or probe used.

The invention also relates to nucleic acid molecules which share substantial sequence identity to the variant alleles identified herein (or their complements) and which also comprise the variant nucleotide at the SNP site. Particularly preferred are nucleic acid molecules and fragments which have at least about 60%, preferably at least about 70, 80 or 85%, more preferably at least about 90%, even more preferably at least about 95%, and most preferably at least about 98% identity with nucleic acid molecules described herein. The percent identity of two nucleotide or amino acid sequences can be determined by aligning the sequences for optimal comparison purposes (e.g., gaps can be introduced in the sequence of a first sequence). The nucleotides or amino acids at corresponding positions are then compared, and the percent identity between the two sequences is a function of the number of identical positions shared by the sequences (i.e., % identity=# of identical positions/total # of positions×100). In certain embodiments, the length of a sequence aligned for comparison purposes is at least 30%, preferably at least 40%, more preferably at least 60%, and even more preferably at least 70%, 80% or 90% of the length of the reference sequence. The actual comparison of the two sequences can be accomplished by well-known methods, for example, using a mathematical algorithm. A preferred, non-limiting example of such a mathematical algorithm is described in Karlin et al., Proc. Natl. Acad. Sci. USA, 90:5873-5877 (1993). Such an algorithm is incorporated into the NBLAST and XBLAST programs (version 2.0) as described in Altschul et al., Nucleic Acids Res., 25:389-3402 (1997). When utilizing BLAST and Gapped BLAST programs, the default parameters of the respective programs (e.g., NBLAST) can be used. See the world wide web at ncbi.nlm.nih.gov. In one embodiment, parameters for sequence comparison can be set at score=100, wordlength=12, or can be varied (e.g., W=5 or W=20).

The term “isolated” is used herein to indicate that the material in question exists in a physical milieu distinct from that in which it occurs in nature. For example, an isolated nucleic acid of the invention may be substantially isolated with respect to the complex cellular milieu in which it naturally occurs. In some instances, the isolated material will form part of a composition (for example, a crude extract containing other substances), buffer system or reagent mix. In other circumstance, the material may be purified to essential homogeneity, for example as determined by PAGE or column chromatography such as HPLC. Preferably, an isolated nucleic acid comprises at least about 50, 80 or 90 percent (on a molar basis) of all macromolecular species present.

I. Novel Polymorphisms of the Invention

Some of the novel polymorphisms of the invention are shown in the Table. Columns one and two show designations for the indicated polymorphism. Column three shows the Genbank or TIGR Accession number for the wild type (or reference) allele. Column four shows the location of the polymorphic site in the nucleic acid sequence with reference to the Genbank or TIGR sequence shown in column three. Column five shows common names for the gene in which the polymorphism is located. Column six shows the polymorphism and a portion of the 3′ and 5′ flanking sequence of the gene. Column seven shows the type of mutation; N, non-sense, S, silent, M, missense. Columns eight and nine show the reference and alternate nucleotides, respectively, at the polymorphic site. Columns ten and eleven show the reference and alternate amino acids, respectively, encoded by the reference and variant, respectively, alleles. Other novel polymorphisms of the invention are shown in FIG. 3.

II. Analysis of Polymorphisms

A. Preparation of Samples

Polymorphisms are detected in a target nucleic acid from an individual being analyzed. For assay of genomic DNA, virtually any biological sample (other than pure red blood cells) is suitable. For example, convenient tissue samples include whole blood, semen, saliva, tears, urine, fecal material, sweat, buccal, skin and hair. For assay of cDNA or mRNA, the tissue sample must be obtained from an organ in which the target nucleic acid is expressed. For example, if the target nucleic acid is a cytochrome P450, the liver is a suitable source.

Many of the methods described below require amplification of DNA from target samples. This can be accomplished by e.g., PCR. See generally PCR Technology: Principles and Applications for DNA Amplification (ed. H. A. Erlich, Freeman Press, NY, N.Y., 1992); PCR Protocols: A Guide to Methods and Applications (eds. Innis, et al., Academic Press, San Diego, Calif., 1990); Mattila et al., Nucleic Acids Res. 19, 4967 (1991); Eckert et al., PCR Methods and Applications 1, 17 (1991); PCR (eds. McPherson et al., IRL Press, Oxford); and U.S. Pat. No. 4,683,202.

Other suitable amplification methods include the ligase chain reaction (LCR) (see Wu and Wallace, Genomics 4, 560 (1989), Landegren et al., Science 241, 1077 (1988), transcription amplification (Kwoh et al., Proc. Natl. Acad. Sci. USA 86, 1173 (1989)), and self-sustained sequence replication (Guatelli et al., Proc. Nat. Acad. Sci. USA, 87, 1874 (1990)) and nucleic acid based sequence amplification (NASBA). The latter two amplification methods involve isothermal reactions based on isothermal transcription, which produce both single stranded RNA (ssRNA) and double stranded DNA (dsDNA) as the amplification products in a ratio of about 30 or 100 to 1, respectively.

B. Detection of Polymorphisms in Target DNA

There are two distinct types of analysis of target DNA for detecting polymorphisms. The first type of analysis, sometimes referred to as de novo characterization, is carried out to identify polymorphic sites not previously characterized (i.e., to identify new polymorphisms). This analysis compares target sequences in different individuals to identify points of variation, i.e., polymorphic sites. By analyzing groups of individuals representing the greatest ethnic diversity among humans and greatest breed and species variety in plants and animals, patterns characteristic of the most common alleles/haplotypes of the locus can be identified, and the frequencies of such alleles/haplotypes in the population can be determined. Additional allelic frequencies can be determined for subpopulations characterized by criteria such as geography, race, or gender. The de novo identification of polymorphisms of the invention is described in the Examples section. The second type of analysis determines which form(s) of a characterized (known) polymorphism are present in individuals under test. There are a variety of suitable procedures, which are discussed in turn.

1. Allele-Specific Probes

The design and use of allele-specific probes for analyzing polymorphisms is described by e.g., Saiki et al., Nature 324, 163-166 (1986); Dattagupta, EP 235,726, Saiki, WO 89/11548. Allele-specific probes can be designed that hybridize to a segment of target DNA from one individual but do not hybridize to the corresponding segment from another individual due to the presence of different polymorphic forms in the respective segments from the two individuals. Hybridization conditions should be sufficiently stringent that there is a significant difference in hybridization intensity between alleles, and preferably an essentially binary response, whereby a probe hybridizes to only one of the alleles. Some probes are designed to hybridize to a segment of target DNA such that the polymorphic site aligns with a central position (e.g., in a 15-mer at the 7 position; in a 16-mer, at either the 8 or 9 position) of the probe. This design of probe achieves good discrimination in hybridization between different allelic forms.

Allele-specific probes are often used in pairs, one member of a pair showing a perfect match to a reference form of a target sequence and the other member showing a perfect match to a variant form. Several pairs of probes can then be immobilized on the same support for simultaneous analysis of multiple polymorphisms within the same target sequence.

2. Tiling Arrays

The polymorphisms can also be identified by hybridization to nucleic acid arrays, some examples of which are described in WO 95/11995. One form of such arrays is described in the Examples section in connection with de novo identification of polymorphisms. The same array or a different array can be used for analysis of characterized polymorphisms. WO 95/11995 also describes subarrays that are optimized for detection of a variant form of a precharacterized polymorphism. Such a subarray contains probes designed to be complementary to a second reference sequence, which is an allelic variant of the first reference sequence. The second group of probes is designed by the same principles as described in the Examples, except that the probes exhibit complementarity to the second reference sequence. The inclusion of a second group (or further groups) can be particularly useful for analyzing short subsequences of the primary reference sequence in which multiple mutations are expected to occur within a short distance commensurate with the length of the probes (e.g., two or more mutations within 9 to 21 bases).

3. Allele-Specific Primers

An allele-specific primer hybridizes to a site on target DNA overlapping a polymorphism and only primes amplification of an allelic form to which the primer exhibits perfect complementarity. See Gibbs, Nucleic Acid Res. 17, 2427-2448 (1989). This primer is used in conjunction with a second primer which hybridizes at a distal site. Amplification proceeds from the two primers, resulting in a detectable product which indicates the particular allelic form is present. A control is usually performed with a second pair of primers, one of which shows a single base mismatch at the polymorphic site and the other of which exhibits perfect complementarity to a distal site. The single-base mismatch prevents amplification and no detectable product is formed. The method works best when the mismatch is included in the 3′-most position of the oligonucleotide aligned with the polymorphism because this position is most destabilizing to elongation from the primer (see, e.g., WO 93/22456).

4. Direct-Sequencing

The direct analysis of the sequence of polymorphisms of the present invention can be accomplished using either the dideoxy chain termination method or the Maxam-Gilbert method (see Sambrook et al., Molecular Cloning, A Laboratory Manual (2nd Ed., CSHP, New York 1989); Zyskind et al., Recombinant DNA Laboratory Manual, (Acad. Press, 1988)).

5. Denaturing Gradient Gel Electrophoresis

Amplification products generated using the polymerase chain reaction can be analyzed by the use of denaturing gradient gel electrophoresis. Different alleles can be identified based on the different sequence-dependent melting properties and electrophoretic migration of DNA in solution. Erlich, ed., PCR Technology, Principles and Applications for DNA Amplification, (W. H. Freeman and Co, New York, 1992), Chapter 7.

6. Single-Strand Conformation Polymorphism Analysis

Alleles of target sequences can be differentiated using single-strand conformation polymorphism analysis, which identifies base differences by alteration in electrophoretic migration of single stranded PCR products, as described in Orita et al., Proc. Nat. Acad. Sci. 86, 2766-2770 (1989). Amplified PCR products can be generated as described above, and heated or otherwise denatured, to form single stranded amplification products. Single-stranded nucleic acids may refold or form secondary structures which are partially dependent on the base sequence. The different electrophoretic mobilities of single-stranded amplification products can be related to base-sequence differences between alleles of target sequences.

7. Single-Base Extension

An alternative method for identifying and analyzing polymorphisms is based on single-base extension (SBE) of a fluorescently-labeled primer coupled with fluorescence resonance energy transfer (FRET) between the label of the added base and the label of the primer. Typically, the method, such as that described by Chen et al., (PNAS 94:10756-61 (1997), incorporated herein by reference) uses a locus-specific oligonucleotide primer labeled on the 5′ terminus with 5-carboxyfluorescein (FAM). This labeled primer is designed so that the 3′ end is immediately adjacent to the polymorphic site of interest. The labeled primer is hybridized to the locus, and single base extension of the labeled primer is performed with fluorescently labeled dideoxyribonucleotides (ddNTPs) in dye-terminator sequencing fashion, except that no deoxyribonucleotides are present. An increase in fluorescence of the added ddNTP in response to excitation at the wavelength of the labeled primer is used to infer the identity of the added nucleotide.

III. Methods of Use

After determining polymorphic form(s) present in an individual at one or more polymorphic sites, this information can be used in a number of methods.

A. Forensics

Determination of which polymorphic forms occupy a set of polymorphic sites in an individual identifies a set of polymorphic forms that distinguishes the individual. See generally National Research Council, The Evaluation of Forensic DNA Evidence (Eds. Pollard et al., National Academy Press, DC, 1996). The more sites that are analyzed, the lower the probability that the set of polymorphic forms in one individual is the same as that in an unrelated individual. Preferably, if multiple sites are analyzed, the sites are unlinked. Thus, polymorphisms of the invention are often used in conjunction with polymorphisms in distal genes. Preferred polymorphisms for use in forensics are biallelic because the population frequencies of two polymorphic forms can usually be determined with greater accuracy than those of multiple polymorphic forms at multi-allelic loci.

The capacity to identify a distinguishing or unique set of forensic markers in an individual is useful for forensic analysis. For example, one can determine whether a blood sample from a suspect matches a blood or other tissue sample from a crime scene by determining whether the set of polymorphic forms occupying selected polymorphic sites is the same in the suspect and the sample. If the set of polymorphic markers does not match between a suspect and a sample, it can be concluded (barring experimental error) that the suspect was not the source of the sample. If the set of markers does match, one can conclude that the DNA from the suspect is consistent with that found at the crime scene. If frequencies of the polymorphic forms at the loci tested have been determined (e.g., by analysis of a suitable population of individuals), one can perform a statistical analysis to determine the probability that a match of suspect and crime scene sample would occur by chance.

p(ID) is the probability that two random individuals have the same polymorphic or allelic form at a given polymorphic site. In biallelic loci, four genotypes are possible: AA, AB, BA, and BB. If alleles A and B occur in a haploid genome of the organism with frequencies x and y, the probability of each genotype in a diploid organism is (see WO 95/12607):

• • Homozygote: p(AA)=x²
  • Homozygote: p(BB)=y²=(1−x)²
  • Single Heterozygote: p(AB)=p(BA)=xy=x(1−x)
  • Both Heterozygotes: p(AB+BA)=2xy=2x(1−x)

The probability of identity at one locus (i.e, the probability that two individuals, picked at random from a population will have identical polymorphic forms at a given locus) is given by the equation:
p(ID)=(x²)²+(2xy)²+(y²)².

These calculations can be extended for any number of polymnorphic forms at a given locus. For example, the probability of identity p(ID) for a 3-allele system where the alleles have the frequencies in the population of x, y and z, respectively, is equal to the sum of the squares of the genotype frequencies:
p(ID)=x⁴+(2xy)²+(2yz)²+(2xz)²+z⁴+y⁴

In a locus of n alleles, the appropriate binomial expansion is used to calculate p(ID) and p(exc).

The cumulative probability of identity (cum p(ID)) for each of multiple unlinked loci is determined by multiplying the probabilities provided by each locus.
cum p(ID)=p(ID1)p(ID2)p(ID3) . . . p(IDn)

The cumulative probability of non-identity for n loci (i.e. the probability that two random individuals will be different at 1 or more loci) is given by the equation:
cump(nonID)=1−cump(ID).

If several polymorphic loci are tested, the cumulative probability of non-identity for random individuals becomes very high (e.g., one billion to one). Such probabilities can be taken into account together with other evidence in determining the guilt or innocence of the suspect.

B. Paternity Testing

The object of paternity testing is usually to determine whether a male is the father of a child. In most cases, the mother of the child is known and thus, the mother's contribution to the child's genotype can be traced. Paternity testing investigates whether the part of the child's genotype not attributable to the mother is consistent with that of the putative father. Paternity testing can be performed by analyzing sets of polymorphisms in the putative father and the child.

If the set of polymorphisms in the child attributable to the father does not match the set of polymorphisms of the putative father, it can be concluded, barring experimental error, that the putative father is not the real father. If the set of polymorphisms in the child attributable to the father does match the set of polymorphisms of the putative father, a statistical calculation can be performed to determine the probability of coincidental match.

The probability of parentage exclusion (representing the probability that a random male will have a polymorphic form at a given polymorphic site that makes him incompatible as the father) is given by the equation (see WO 95/12607):
p(exc)=xy(1−xy)
where x and y are the population frequencies of alleles A and B of a biallelic polymorphic site.

(At a triallelic site p(exc)=xy(1−xy)+yz(1−yz)+xz(1−xz)+3xyz(1−xyz))), where x, y and z and the respective population frequencies of alleles A, B and C).

The probability of non-exclusion is
p(non-exc)=1−p(exc)

The cumulative probability of non-exclusion (representing the value obtained when n loci are used) is thus:
cump(non-exc)=p(non-exc1)p(non-exc2)p(non-exc3) . . . p(non-excn)

The cumulative probability of exclusion for n loci (representing the probability that a random male will be excluded)
cump(exc)=1−cump(non-exc).

If several polymorphic loci are included in the analysis, the cumulative probability of exclusion of a random male is very high. This probability can be taken into account in assessing the liability of a putative father whose polymorphic marker set matches the child's polymorphic marker set attributable to his/her father.

C. Correlation of Polymorphisms with Phenotypic Traits

The polymorphisms of the invention may contribute to the phenotype of an organism in different ways. Some polymorphisms occur within a protein coding sequence and contribute to phenotype by affecting protein structure. The effect may be neutral, beneficial or detrimental, or both beneficial and detrimental, depending on the circumstances. For example, a heterozygous sickle cell mutationi confers resistance to malaria, but a homozygous sickle cell mutation is usually lethal. Other polymorphisms occur in noncoding regions but may exert phenotypic effects indirectly via influence on replication, transcription, and translation. A single polymorphism may affect more than one phenotypic trait. Likewise, a single phenotypic trait may be affected by polymorphisms in different genes. Further, some polymorphisms predispose an individual to a distinct mutation that is causally related to a certain phenotype.

Phenotypic traits include diseases that have known but hitherto unmapped genetic components (e.g., agammaglobulimenia, diabetes insipidus, Lesch-Nyhan syndrome, muscular dystrophy, Wiskott-Aldrich syndrome, Fabry's disease, familial hypercholesterolemia, polycystic kidney disease, hereditary spherocytosis, von Willebrand's disease, tuberous sclerosis, hereditary hemorrhagic telangiectasia, familial colonic polyposis, Ehlers-Danlos syndrome, osteogenesis imperfecta, and acute intermittent porphyria). Phenotypic traits also include symptoms of, or susceptibility to, multifactorial diseases of which a component is or may be genetic, such as autoimmune diseases, inflammation, cancer, diseases of the nervous system, and infection by pathogenic microorganisms. Some examples of autoimmune diseases include rheumatoid arthritis, multiple sclerosis, diabetes (insulin-dependent and non-independent), systemic lupus erythematosus and Graves disease. Some examples of cancers include cancers of the bladder, brain, breast, colon, esophagus, kidney, leukemia, liver, lung, oral cavity, ovary, pancreas, prostate, skin, stomach and uterus. Phenotypic traits also include characteristics such as longevity, appearance (e.g., baldness, obesity), strength, speed, endurance, fertility, and susceptibility or receptivity to particular drugs or therapeutic treatments.

The correlation of one or more polymorphisms with phenotypic traits can be facilitated by knowledge of the gene product of the wild type (reference) gene. The genes in which cSNPs of the present invention have been identified are genes which have been previously sequenced and characterized in one of their allelic forms.

Correlation is performed for a population of individuals who have been tested for the presence or absence of a phenotypic trait of interest and for polymorphic markers sets. To perform such analysis, the presence or absence of a set of polymorphisms (i.e. a polymorphic set) is determined for a set of the individuals, some of whom exhibit a particular trait, and some of which exhibit lack of the trait. The alleles of each polymorphism of the set are then reviewed to determine whether the presence or absence of a particular allele is associated with the trait of interest. Correlation can be performed by standard statistical methods such as a κ-squared test and statistically significant correlations between polymorphic form(s) and phenotypic characteristics are noted. For example, it might be found that the presence of allele A1 at polymorphism A correlates with heart disease. As a further example, it might be found that the combined presence of allele A1 at polymorphism A and allele B1 at polymorphism B correlates with increased milk production of a farm animal.

Such correlations can be exploited in several ways. In the case of a strong correlation between a set of one or more polymorphic forms and a disease for which treatment is available, detection of the polymorphic form set in a human or animal patient may justify immediate administration of treatment, or at least the institution of regular monitoring of the patient. Detection of a polymorphic form correlated with serious disease in a couple contemplating a family may also be valuable to the couple in their reproductive decisions. For example, the female partner might elect to undergo in vitro fertilization to avoid the possibility of transmitting such a polymorphism from her husband to her offspring. In the case of a weaker, but still statistically significant correlation between a polymorphic set and human disease, immediate therapeutic intervention or monitoring may not be justified. Nevertheless, the patient can be motivated to begin simple life-style changes (e.g., diet, exercise) that can be accomplished at little cost to the patient but confer potential benefits in reducing the risk of conditions to which the patient may have increased susceptibility by virtue of variant alleles. Identification of a polymorphic set in a patient correlated with enhanced receptiveness to one of several treatment regimes for a disease indicates that this treatment regime should be followed.

For animals and plants, correlations between characteristics and phenotype are useful for breeding for desired characteristics. For example, Beitz et al., U.S. Pat. No. 5,292,639 discuss use of bovine mitochondrial polymorphisms in a breeding program to improve milk production in cows. To evaluate the effect of mtDNA D-loop sequence polymorphism on milk production, each cow was assigned a value of 1 if variant or 0 if wildtype with respect to a prototypical mitochondrial DNA sequence at each of 17 locations considered. Each production trait was analyzed individually with the following animal model:
Y_ijkpn=μ+YS_i+P_j+X_k+β₁+ . . . β₁₇+PE_n+a_n+e_p
where Y_ijknp is the milk, fat, fat percentage, SNF, SNF percentage, energy concentration, or lactation energy record; μ is an overall mean; YS_i is the effect common to all cows calving in year-season; X_k is the effect common to cows in either the high or average selection line; β₁ to β₁₇ are the binomial regressions of production record on mtDNA D-loop sequence polymorphisms; PE_n is permanent environmental effect common to all records of cow n; a_n is effect of animal n and is composed of the additive genetic contribution of sire and dam breeding values and a Mendelian sampling effect; and e_p is a random residual. It was found that eleven of seventeen polymorphisms tested influenced at least one production trait. Bovines having the best polymorphic forms for milk production at these eleven loci are used as parents for breeding the next generation of the herd.

D. Genetic Mapping of Phenotypic Traits

The previous section concerns identifying correlations between phenotypic traits and polymorphisms that directly or indirectly contribute to those traits. The present section describes identification of a physical linkage between a genetic locus associated with a trait of interest and polymorphic markers that are not associated with the trait, but are in physical proximity with the genetic locus responsible for the trait and co-segregate with it. Such analysis is useful for mapping a genetic locus associated with a phenotypic trait to a chromosomal position, and thereby cloning gene(s) responsible for the trait. See Lander et al., Proc. Natl. Acad. Sci. (USA) 83, 7353-7357 (1986); Lander et al., Proc. Natl. Acad. Sci. (USA) 84, 2363-2367 (1987); Donis-Keller et al., Cell 51, 319-337 (1987); Lander et al., Genetics 121, 185-199 (1989)). Genes localized by linkage can be cloned by a process known as directional cloning. See Wainwright, Med. J. Australia 159, 170-174 (1993); Collins, Nature Genetics 1, 3-6 (1992).

Linkage studies are typically performed on members of a family. Available members of the family are characterized for the presence or absence of a phenotypic trait and for a set of polymorphic markers. The distribution of polymorphic markers in an informative meiosis is then analyzed to determine which polymorphic markers co-segregate with a phenotypic trait. See, e.g., Kerem et al., Science 245, 1073-1080 (1989); Monaco et al., Nature 316, 842 (1985); Yamoka et al., Neurology 40, 222-226 (1990); Rossiter et al., FASEB Journal 5, 21-27 (1991).

Linkage is analyzed by calculation of LOD (log of the odds) values. A lod value is the relative likelihood of obtaining observed segregation data for a marker and a genetic locus when the two are located at a recombination fraction θ, versus the situation in which the two are not linked, and thus segregating independently (Thompson & Thompson, Genetics in Medicine (5th ed, W. B. Saunders Company, Philadelphia, 1991); Strachan, “Mapping the human genome” in The Human Genome (BIOS Scientific Publishers Ltd, Oxford), Chapter 4). A series of likelihood ratios are calculated at various recombination fractions (θ), ranging from θ=0.0 (coincident loci) to θ=0.50 (unlinked). Thus, the likelihood at a given value of θ is: probability of data if loci linked at θ to probability of data if loci unlinked. The computed likelihoods are usually expressed as the log₁₀ of this ratio (i.e., a lod score). For example, a lod score of 3 indicates 1000:1 odds against an apparent observed linkage being a coincidence. The use of logarithms allows data collected from different families to be combined by simple addition. Computer programs are available for the calculation of lod scores for differing values of θ (e.g., LIPED, MLINK (Lathrop, Proc. Nat. Acad. Sci. (USA) 81, 3443-3446 (1984)). For any particular lod score, a recombination fraction may be determined from mathematical tables. See Smith et al., Mathematical tables for research workers in human genetics (Churchill, London, 1961); Smith, Ann. Hum. Genet. 32, 127-150 (1968). The value of θ at which the lod score is the highest is considered to be the best estimate of the recombination fraction.

Positive lod score values suggest that the two loci are linked, whereas negative values suggest that linkage is less likely (at that value of θ) than the possibility that the two loci are unlinked. By convention, a combined lod score of +3 or greater (equivalent to greater than 1000:1 odds in favor of linkage) is considered definitive evidence that two loci are linked. Similarly, by convention, a negative lod score of −2 or less is taken as definitive evidence against linkage of the two loci being compared. Negative linkage data are useful in excluding a chromosome or a segment thereof from consideration. The search focuses on the remaining non-excluded chromosomal locations.

IV. Modified Polypeptides and Gene Sequences

The invention further provides variant forms of nucleic acids and corresponding proteins. The nucleic acids comprise one of the sequences described in the Table, column 5, in which the polymorphic position is occupied by one of the alternative bases for that position. Some nucleic acids encode full-length variant forms of proteins. Similarly, variant proteins have the prototypical amino acid sequences encoded by nucleic acid sequences shown in the Table, column 5, (read so as to be in-frame with the full-length coding sequence of which it is a component) except at an amino acid encoded by a codon including one of the polymorphic positions shown in the Table. That position is occupied by the amino acid coded by the corresponding codon in any of the alternative forms shown in the Table.

Variant genes can be expressed in an expression vector in which a variant gene is operably linked to a native or other promoter. Usually, the promoter is a eukaryotic promoter for expression in a mammalian cell. The transcription regulation sequences typically include a heterologous promoter and optionally an enhancer which is recognized by the host. The selection of an appropriate promoter, for example trp, lac, phage promoters, glycolytic enzyme promoters and tRNA promoters, depends on the host selected. Commercially available expression vectors can be used. Vectors can include host-recognized replication systems, amplifiable genes, selectable markers, host sequences useful for insertion into the host genome, and the like.

The means of introducing the expression construct into a host cell varies depending upon the particular construction and the target host. Suitable means include fusion, conjugation, transfection, transduction, electroporation or injection, as described in Sambrook, supra. A wide variety of host cells can be employed for expression of the variant gene, both prokaryotic and eukaryotic. Suitable host cells include bacteria such as E. coli, yeast, filamentous fuigi, insect cells, mammalian cells, typically immortalized, e.g., mouse, CHO, human and monkey cell lines and derivatives thereof. Preferred host cells are able to process the variant gene product to produce an appropriate mature polypeptide. Processing includes glycosylation, ubiquitination, disulfide bond formation, general post-translational modification, and the like. As used herein, “gene product” includes mRNA, peptide and protein products.

The protein may be isolated by conventional means of protein biochemistry and purification to obtain a substantially pure product, i.e., 80, 95 or 99% free of cell component contaminants, as described in Jacoby, Methods in Enzymology Volume 104, Academic Press, New York (1984); Scopes, Protein Purification, Principles and Practice, 2nd Edition, Springer-Verlag, New York (1987); and Deutscher (ed), Guide to Protein Purification, Methods in Enzymology, Vol. 182 (1990). If the protein is secreted, it can be isolated from the supernatant in which the host cell is grown. If not secreted, the protein can be isolated from a lysate of the host cells.

The invention further provides transgenic nonhuman animals capable of expressing an exogenous variant gene and/or having one or both alleles of an endogenous variant gene inactivated. Expression of an exogenous variant gene is usually achieved by operably linking the gene to a promoter and optionally an enhancer, and microinjecting the construct into a zygote. See Hogan et al., “Manipulating the Mouse Embryo, A Laboratory Manual,” Cold Spring Harbor Laboratory. Inactivation of endogenous variant genes can be achieved by forming a transgene in which a cloned variant gene is inactivated by insertion of a positive selection marker. See Capecchi, Science 244, 1288-1292 (1989). The transgene is then introduced into an embryonic stem cell, where it undergoes homologous recombination with an endogenous variant gene. Mice and other rodents are preferred animals. Such animals provide useful drug screening systems.

In addition to substantially full-length polypeptides expressed by variant genes, the present invention includes biologically active fragments of the polypeptides, or analogs thereof, including organic molecules which simulate the interactions of the peptides. Biologically active fragments include any portion of the full-length polypeptide which confers a biological function on the variant gene product, including ligand binding, and antibody binding. Ligand binding includes binding by nucleic acids, proteins or polypeptides, small biologically active molecules, or large cellular structures.

Polyclonal and/or monoclonal antibodies that specifically bind to variant gene products but not to corresponding prototypical gene products are also provided. Antibodies can be made by injecting mice or other animals with the variant gene product or synthetic peptide fragments thereof. Monoclonal antibodies are screened as are described, for example, in Harlow & Lane, Antibodies, A Laboratory Manual, Cold Spring Harbor Press, New York (1988); Goding, Monoclonal antibodies, Principles and Practice (2d ed.) Academic Press, New York (1986). Monoclonal antibodies are tested for specific immunoreactivity with a variant gene product and lack of immunoreactivity to the corresponding prototypical gene product. These antibodies are useful in diagnostic assays for detection of the variant form, or as an active ingredient in a pharmaceutical composition.

V. Kits

The invention further provides kits comprising at least one allele-specific oligonucleotide as described herein. Often, the kits contain one or more pairs of allele-specific oligonucleotides hybridizing to different forms of a polymorphism. In some kits, the allele-specific oligonucleotides are provided immobilized to a substrate. For example, the same substrate can comprise allele-specific oligonucleotide probes for detecting at least 10, 100 or all of the polymorphisms shown in the Table. Optional additional components of the kit include, for example, restriction enzymes, reverse-transcriptase or polymerase, the substrate nucleoside triphosphates, means used to label (for example, an avidin-enzyme conjugate and enzyme substrate and chromogen if the label is biotin), and the appropriate buffers for reverse transcription, PCR, or hybridization reactions. Usually, the kit also contains instructions for carrying out the methods.

The thrombospondins are a family of extracellular matrix (ECM) glycoproteins that modulate many cell behaviors including adhesion, migration, and proliferation. Thrombospondins (also known as thrombin sensitive proteins or TSPs) are large molecular weight glycoproteins composed of three identical disulfide-linked polypeptide chains. TSPs are stored in the alpha-granules of platelets and secreted by a variety of mesenchymal and epithelial cells (Majack et al., Cell Membrane 3:57-77 (1987)). Platelets secrete TSPs when activated in the blood by such physiological agonists such as thrombin. TSPs have lectin properties and a broad function in the regulation of fibrinolysis and as a component of the ECM, and are one of a group of ECM proteins which have adhesive properties. TSPs bind to fibronectin and fibrinogen (Lahav et al., Eur J Biochem 145:151-6 (1984)), and these proteins are known to be involved in platelet adhesion to substratum and platelet aggregation (Leung, J Clin Invest 74:1764-1772 (1986)).

Recent work has implicated TSPs in response of cells to growth factors. Submitogenic doses of PDGF induce a rapid but transitory, increase in TSP synthesis and secretion by rat aortic smooth muscle cells (Majack et al., J Biol Chem 101: 1059-70 (1985)). PDGF responsiveness to TSP synthesis in glial cells has also been shown (Asch et al., Proc Natl Acad Sci 83:2904-8 (1986)). TSP mRNA levels rise rapidly in response to PDGF (Majack et al., J. Biol Chem 262:8821-5 (1987)). TSPs act synergistically with epidermal growth factor to increase DNA synthesis in smooth muscle cells (Majack et al., Proc Natl Acad Sci 83:9050-4 (1986)), and monoclonal antibodies to TSPs inhibit smooth muscle cell proliferation (Majack et al., J Biol Chem 106:415-22 (1988)). TSPs modulate local adhesions in endothelial cells, and TSPs, particularly TSP-1 primarily derived from platelet granules, are known to be an important activator of transforming growth factor beta-1 (TGFB-1) (Crawford et al., Cell 93:1159 (1998)) and appear to be a potential link between platelet-thrombosis and development of atherosclerosis.

To determine pivotal genes associated with premature coronary artery disease, we analyzed DNA from 347 patients with MI or coronary revascularization before age 40 (men) or 45 (women) and 422 general population controls. Cases were drawn (one per family) from a retrospective collection of sibling pairs with premature CAD. Controls were ascertained through random-digit dialing. Both cases and controls were Caucasian. A complete database of phenotypic and laboratory variables for the affected patients afforded logistic regression to control for age, diabetes, body mass index, gender.

Thrombospondin (TSP) 4 and 1 emerged as important SNPs associated with premature CAD and MI. For CAD, 148 of 347 patients carried at least one copy of the TSP-4 variant compared with 142 of 422 control subjects; adjusted odds ratio 1.47, p=0.01. For premature MI, the association was even stronger: 91 of 187 cases vs. 142 of 422 controls had the variant; adjusted odds ratio 2.08, p=0.0003. The TSP-1 SNP was rare. Nonetheless, homozygosity for the variant allele gave an adjusted odds ratio of 9.5, p=0.04.

Specific reference nucleotide (SEQ ID NO: 1) and amino acid (SEQ ID NO: 2) sequences for TSP-1 are shown in FIGS. 1A-1D. Specific reference nucleotide (SEQ ID NO: 3) and amino acid (SEQ ID NO: 4) sequences for TSP-4 are shown in FIGS. 2A-2C. It is understood that the invention is not limited by these exemplified reference sequences, as variants of these sequences which differ at locations other than the SNP sites identified herein can also be utilized. The skilled artisan can readily determine the SNP sites in these other reference sequences which correspond to the SNP sites identified herein by aligning the sequence of interest with the reference sequences specifically disclosed herein, and programs for performing such alignments are commercially available. For example, the ALIGN program in the GCG software package can be used, utilizing a PAM120 weight residue table, a gap length penalty of 12 and a gap penalty of 4, for example.

Two SNPs have been specifically studied as described herein. The first (G334u4) is a change from A (reference nucleotide) to G (alternate or variant nucleotide) at nucleotide position 2210 of the nucleic acid sequence of TSP—I (FIGS. 1A-1D), resulting in a missense amino acid mutation from asparagine (reference) to serine (alternate) at amino acid 700. The second SNP (G355u2) is a change from G (reference) to C (alternate) at nucleotide position 1186 of the nucleic acid sequence of TSP-4 (FIGS. 2A-2C), resulting in a missense amino acid alteration from alanine (reference) to proline (alternate) at amino acid 387. With respect to the G355u2 SNP, individuals with CAD carried at least one copy of the variant “C” allele more frequently than control individuals (43% as compared with 34%). With respect to the G355u2 SNP, individuals with MI carried at least one copy of the variant “C” allele more frequently than control individuals (49% as compared with 34%). With respect to the G334u4 SNP, individuals with CAD carried two copies of the variant “G” allele more frequently than control individuals (1.7% as compared with 0.2%). With respect to the G334u4 SNP, individuals with MI carried two copies of the variant “G” allele more frequently than control individuals (2% as compared with 0.2%).

As used herein, the term “polymorphism” refers to the occurrence of two or more genetically determined alternative sequences or alleles in a population. A polymorphic marker or site is the locus at which divergence occurs. Preferred markers have at least two alleles, each occurring at frequency of greater than 1%, and more preferably greater than 10% or 20% of a selected population. A polymorphic locus may be as small as one base pair, in which case it is referred to as a single nucleotide polymorphism (SNP).

Thus, the invention relates to a method for predicting the likelihood that an individual will have a vascular disease, or for aiding in the diagnosis of a vascular disease, or predicting the likelihood of having altered symptomology associated with a vascular disease, comprising the steps of obtaining a DNA sample from an individual to be assessed and determining the nucleotide present at one or more of nucleotide positions 2210 of the TSP-1 gene or 1186 of the TSP-4 gene. In a preferred embodiment, the nucleotides present at both of these nucleotide positions are determined. In one embodiment the TSP-1 gene has the nucleotide sequence of SEQ ID NO: 1 and the TSP-4 gene has the nucleotide sequence of SEQ ID NO: 3. The presence of one or more of a G (the variant nucleotide) at position 2210 of SEQ ID NO: 1 or a C (the variant nucleotide) at position 1186 of SEQ ID NO: 1186 indicates that the individual has a greater likelihood of having a vascular disease, or a greater likelihood of having severe symptomology associated with a vascular disease, than if that individual had the reference nucleotide at one or more of these positions. Conversely, the presence of one or more of an A (the reference nucleotide) at position 2210 of SEQ ID NO: 1 or a G (the reference nucleotide) at position 1186 of SEQ ID NO: 3 indicates that the individual has a reduced likelihood of having a vascular disease or a likelihood of having reduced symptomology associated with a vascular disease than if that individual had the variant nucleotide at one or more of these positions.

In a particular embodiment, the individual is an individual at risk for development of a vascular disease. In another embodiment the individual exhibits clinical symptomology associated with a vascular disease. In one embodiment, the individual has been clinically diagnosed as having a vascular disease. Vascular diseases include, but are not limited to, atherosclerosis, coronary heart disease, myocardial infarction (MI), stroke, peripheral vascular diseases, venous thromboembolism and puhnonary embolism. In preferred embodiments, the vascular disease is CAD or MI.

The genetic material to be assessed can be obtained from any nucleated cell from the individual. For assay of genomic DNA, virtually any biological sample (other than pure red blood cells) is suitable. For example, convenient tissue samples include whole blood, semen, saliva, tears, urine, fecal material, sweat, skin and hair. For assay of cDNA or mRNA, the tissue sample must be obtained from a tissue or organ in which the target nucleic acid is expressed.

Many of the methods described herein require amplification of DNA from target samples. This can be accomplished by e.g., PCR. See generally PCR Technology: Principles and Applications for DNA Amplification (ed. H. A. Erlich, Freeman Press, NY, N.Y., 1992); PCR Protocols: A Guide to Methods and Applications (eds. Innis, et al., Academic Press, San Diego, Calif., 1990); Mattila et al., Nucleic Acids Res. 19, 4967 (1991); Eckert et al., PCR Methods and Applications 1, 17 (1991); PCR (eds. McPherson et al., IRL Press, Oxford); and U.S. Pat. No. 4,683,202.

Other suitable amplification methods include the ligase chain reaction (LCR) (see Wu and Wallace, Genomics 4, 560 (1989), Landegren et al., Science 241, 1077 (1988), transcription amplification (Kwoh et al., Proc. Natl. Acad. Sci. USA 86, 1173 (1989)), and self-sustained sequence replication (Guatelli et al., Proc. Nat. Acad. Sci. USA, 87, 1874 (1990)) and nucleic acid based sequence amplification (NASBA). The latter two amplification methods involve isothermal reactions based on isothermal transcription, which produce both single stranded RNA (ssRNA) and double stranded DNA (dsDNA) as the amplification products in a ratio of about 30 or 100 to 1, respectively.

The nucleotide which occupies the polymorphic site of interest (e.g., nucleotide position 2210 in TSP-1 and/or nucleotide position 1186 in TSP-4) can be identified by a variety of methods, such as Southern analysis of genomic DNA; direct mutation analysis by restriction enzyme digestion; Northern analysis of RNA; denaturing high pressure liquid chromatography (DHPLC); gene isolation and sequencing; hybridization of an allele-specific oligonucleotide with amplified gene products; single base extension (SBE). In a preferred embodiment, determination of the allelic form of TSP is carried out using SBE-FRET methods as described herein, or using chip-based oligonucleotide arrays as described herein.

The invention also relates to a method for predicting the likelihood that an individual will have a vascular disease, or for aiding in the diagnosis of a vascular disease, or predicting the likelihood of having altered symptomology associated with a vascular disease, comprising the steps of obtaining a biological sample comprising TSP-1 and/or TSP-4 protein or relevant portion thereof from an individual to be assessed and determining the amino acid present at one or more of amino acid positions 700 of the TSP-1 gene product (e.g., as exemplified by SEQ ID NO: 2) or 387 of the TSP-4 gene product (e.g., as exemplified by SEQ ID NO: 4). In a preferred embodiment, the amino acids present at both of these amino acid positions are determined. As used herein, the term “relevant portion” of the TSP-1 and TSP-4 proteins is intended to encompass any portion of the protein which comprises the polymorphic amino acid positions. The presence of one or more of a serine (the variant amino acid) at position 700 of SEQ ID NO: 2, or a proline (the variant amino acid) at position 387 of SEQ ID NO: 4 indicates that the individual has a greater likelihood of having a vascular disease, or a greater likelihood of having severe symptomology associated with a vascular disease, than if that individual had the reference amino acid at one or more of these positions. Conversely, the presence of one or more of an asparagine (the reference amino acid) at position 700 of SEQ ID NO: 2, or an alanine (the reference amino acid) at position 387 of SEQ ID NO: 4 indicates that the individual has a reduced likelihood of having a vascular disease or a likelihood of having reduced symptomology associated with a vascular disease, than if that individual had the varaint amino acid at one or more of these positions.

In a particular embodiment, the individual is an individual at risk for development of a vascular disease. In another embodiment the individual exhibits clinical symptomology associated with a vascular disease. In one embodiment, the individual has been clinically diagnosed as having a vascular disease.

In this embodiment of the invention, the biological sample contains protein molecules from the test subject. In vitro techniques for detection of protein include enzyme linked immunosorbent assays (ELISAs), Western blots, immunoprecipitations and immunofluorescence. Furthermore, in vivo techniques for detection of protein include introducing into a subject a labeled anti-protein antibody. For example, the antibody can be labeled with a radioactive marker whose presence and location in a subject can be detected by standard imaging techniques. Polyclonal and/or monoclonal antibodies that specifically bind to variant gene products but not to corresponding reference gene products, and vice versa, are also provided. Antibodies can be made by injecting mice or other animals with the variant gene product or synthetic peptide fragments thereof comprising the variant portion. Monoclonal antibodies are screened as are described, for example, in Harlow & Lane, Antibodies, A Laboratory Manual, Cold Spring Harbor Press, New York (1988); Goding, Monoclonal antibodies, Principles and Practice (2d ed.) Academic Press, New York (1986). Monoclonal antibodies are tested for specific immunoreactivity with a variant gene product and lack of immunoreactivity to the corresponding prototypical gene product. These antibodies are useful in diagnostic assays for detection of the variant form, or as an active ingredient in a pharmaceutical composition.

The polymorphisms of the invention may be associated with vascular disease in different ways. The polymorphisms may exert phenotypic effects indirectly via influence on replication, transcription, and translation. Additionally, the described polymorphisms may predispose an individual to a distinct mutation that is causally related to a certain phenotype, such as susceptibility or resistance to vascular disease and related disorders. The discovery of the polymorphisms and their correlation with CAD and MI facilitates biochemical analysis of the variant and reference forms and the development of assays to characterize the variant and reference forms and to screen for pharmaceutical agents that interact directly with one or another form of the protein.

Alternatively, these particular polymorphisms may belong to a group of two or more polymorphisms in the TSP gene(s) which contributes to the presence, absence or severity of vascular disease. An assessment of other polymorphisms within the TSP gene(s) can be undertaken, and the separate and combined effects of these polymorphisms, as well as alternations in other, distinct genes, on the vascular disease phenotype can be assessed.

Correlation between a particular phenotype, e.g., the CAD or MI phenotype, and the presence or absence of a particular allele is performed for a population of individuals who have been tested for the presence or absence of the phenotype. Correlation can be performed by standard statistical methods such as a Chi-squared test and statistically significant correlations between polymorphic form(s) and phenotypic characteristics are noted. This correlation can be exploited in several ways. In the case of a strong correlation between a particular polymorphic form, e.g., the variant allele for TSP-1 and/or TSP-4, and a disease for which treatment is available, detection of the polymorphic form in an individual may justify immediate administration of treatment, or at least the institution of regular monitoring of the individual. Detection of a polymorphic form correlated with a disorder in a couple contemplating a family may also be valuable to the couple in their reproductive decisions. For example, the female partner might elect to undergo in vitro fertilization to avoid the possibility of transmitting such a polymorphism from her husband to her offspring. In the case of a weaker, but still statistically significant correlation between a polymorphic form and a particular disorder, immediate therapeutic intervention or monitoring may not be justified. Nevertheless, the individual can be motivated to begin simple life-style changes (e.g., diet modification, therapy or counseling) that can be accomplished at little cost to the individual but confer potential benefits in reducing the risk of conditions to which the individual may have increased susceptibility by virtue of the particular allele. Furthermore, identification of a polymorphic form correlated with enhanced receptiveness to one of several treatment regimes for a disorder indicates that this treatment regimen should be followed for the individual in question.

Furthermore, it may be possible to identify a physical linkage between a genetic locus associated with a trait of interest (e.g., CAD or MI) and polymorphic markers that are or are not associated with the trait, but are in physical proximity with the genetic locus responsible for the trait and co-segregate with it. Such analysis is useful for mapping a genetic locus associated with a phenotypic trait to a chromosomal position, and thereby cloning gene(s) responsible for the trait. See Lander et al., Proc. Natl. Acad. Sci. (USA) 83, 7353-7357 (1986); Lander et al., Proc. Natl. Acad. Sci. (USA) 84, 2363-2367 (1987); Donis-Keller et al., Cell 51, 319-337 (1987); Lander et al., Genetics 121, 185-199 (1989)). Genes localized by linkage can be cloned by a process known as directional cloning. See Wainwright, Med. J Australia 159, 170-174 (1993); Collins, Nature Genetics 1, 3-6 (1992). Linkage studies are discussed in more detail above.

In another embodiment, the invention relates to pharmaceutical compositions comprising a reference TSP-1 and/or TSP-4 gene or gene product for use in the treatment of vascular disease, e.g., CAD and MI. As used herein, a reference TSP gene product is intended to mean gene products which are encoded by the reference allele of the TSP gene. In addition to substantially full-length polypeptides expressed by the genes, the present invention includes biologically active fragments of the polypeptides, or analogs thereof, including organic molecules which simulate the interactions of the peptides. Biologically active fragments include any portion of the full-length polypeptide which confers a biological function on the variant gene product, including ligand binding, and antibody binding. Ligand binding includes binding by nucleic acids, proteins or polypeptides, small biologically active molecules, or large cellular structures.

For instance, the polypeptide or protein, or fragment thereof, of the present invention can be formulated with a physiologically acceptable medium to prepare a pharmaceutical composition. The particular physiological medium may include, but is not limited to, water, buffered saline, polyols (e.g., glycerol, propylene glycol, liquid polyethylene glycol) and dextrose solutions. The optimum concentration of the active ingredient(s) in the chosen medium can be determined empirically, according to procedures well known to medicinal chemists, and will depend on the ultimate pharmaceutical formulation desired. Methods of introduction of exogenous peptides at the site of treatment include, but are not limited to, intradernal, intramuscular, intraperitoneal, intravenous, subcutaneous, oral and intranasal. Other suitable methods of introduction can also include rechargeable or biodegradable devices and slow release polymeric devices. The pharmaceutical compositions of this invention can also be administered as part of a combinatorial therapy with other agents and treatment regimens.

The invention further pertains to compositions, e.g., vectors, comprising a nucleotide sequence encoding reference or variant TSP-1 and/or TSP-4 gene products. For example, reference genes can be expressed in an expression vector in which a reference gene is operably linked to a native or other promoter. Usually, the promoter is a eukaryotic promoter for expression in a mammalian cell. The transcription regulation sequences typically include a heterologous promoter and optionally an enhancer which is recognized by the host. The selection of an appropriate promoter, for example trp, lac, phage promoters, glycolytic enzyme promoters and tRNA promoters, depends on the host selected. Commercially available expression vectors can be used. Vectors can include host-recognized replication systems, amplifiable genes, selectable markers, host sequences useful for insertion into the host genome, and the like.

The means of introducing the expression construct into a host cell varies depending upon the particular construction and the target host. Suitable means include fusion, conjugation, transfection, transduction, electroporation or injection, as described in Sambrook, supra. A wide variety of host cells can be employed for expression of the variant gene, both prokaryotic and eukaryotic. Suitable host cells include bacteria such as E. coli, yeast, filamentous fungi, insect cells, mammalian cells, typically immortalized, e.g., mouse, CHO, human and monkey cell lines and derivatives thereof. Preferred host cells are able to process the variant gene product to produce an appropriate mature polypeptide. Processing includes glycosylation, ubiquitination, disulfide bond formation, general post-translational modification, and the like.

It is also contemplated that cells can be engineered to express the reference allele of the invention by gene therapy methods. For example, DNA encoding the reference TSP gene product, or an active fragment or derivative thereof, can be introduced into an expression vector, such as a viral vector, and the vector can be introduced into appropriate cells in an animal. In such a method, the cell population can be engineered to inducibly or constitutively express active reference TSP gene product. In a preferred embodiment, the vector is delivered to the bone marrow, for example as described in Corey et al. (Science 244:1275-1281 (1989)).

The invention further relates to the use of compositions (i.e., agonists) which enhance or increase the activity of the reference (or variant) TSP (e.g., TSP-1 or TSP-4) gene product, or a functional portion thereof, for use in the treatment of vascular disease. The invention also relates to the use of compositions (i.e., antagonists) which reduce or decrease the activity of the variant (or reference) TSP (e.g., TSP-1 or TSP-4) gene product, or a functional portion thereof, for use in the treatment of vascular disease.

The invention also relates to constructs which comprise a vector into which a sequence of the invention has been inserted in a sense or antisense orientation. For example, a vector comprising a nucleotide sequence which is antisense to the variant TSP-1 or TSP-4 allele may be used as an antagonist of the activity of the TSP-1 or TSP-4 variant allele. Alternatively, a vector comprising a nucleotide sequence of the TSP-1 or TSP-4 reference allele may be used therapeutically to treat vascular diseases. As used herein, the term “vector” refers to a nucleic acid molecule capable of transporting another nucleic acid to which it has been linked. One type of vector is a “plasmid”, which refers to a circular double stranded DNA loop into which additional DNA segments can be ligated. Another type of vector is a viral vector, wherein additional DNA segments can be ligated into the viral genome. Certain vectors are capable of autonomous replication in a host cell into which they are introduced (e.g., bacterial vectors having a bacterial origin of replication and episomal mammalian vectors). Other vectors (e.g., non-episomal mammalian vectors) are integrated into the genome of a host cell upon introduction into the host cell, and thereby are replicated along with the host genome. Moreover, certain vectors, expression vectors, are capable of directing the expression of genes to which they are operably linked. In general, expression vectors of utility in recombinant DNA techniques are often in the form of plasmids (vectors). However, the invention is intended to include such other forms of expression vectors, such as viral vectors (e.g., replication defective retroviruses, adenoviruses and adeno-associated viruses) that serve equivalent functions.

Preferred recombinant expression vectors of the invention comprise a nucleic acid of the invention in a form suitable for expression of the nucleic acid in a host cell. This means that the recombinant expression vectors include one or more regulatory sequences, selected on the basis of the host cells to be used for expression, which is operably linked to the nucleic acid sequence to be expressed. Within a recombinant expression vector, “operably linked” is intended to mean that the nucleotide sequence of interest is linked to the regulatory sequence(s) in a manner which allows for expression of the nucleotide sequence (e.g., in an in vitro transcription/translation system or in a host cell when the vector is introduced into the host cell). The term “regulatory sequence” is intended to include promoters, enhancers and other expression control elements (e.g., polyadenylation signals). Such regulatory sequences are described, for example, in Goeddel, Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990). Regulatory sequences include those which direct constitutive expression of a nucleotide sequence in many types of host cell and those which direct expression of the nucleotide sequence only in certain host cells (e.g., tissue-specific regulatory sequences). It will be appreciated by those skilled in the art that the design of the expression vector can depend on such factors as the choice of the host cell to be transformed, the level of expression of protein desired, etc.

The expression vectors of the invention can be introduced into host cells to thereby produce proteins or peptides, including fusion proteins or peptides, encoded by nucleic acids as described herein. The recombinant expression vectors of the invention can be designed for expression of a polypeptide of the invention in prokaryotic or eukaryotic cells, e.g., bacterial cells such as E. coli, insect cells (using baculovirus expression vectors), yeast cells or mammalian cells. Suitable host cells are discussed further in Goeddel, supra. Alternatively, the recombinant expression vector can be transcribed and translated in vitro, for example using T7 promoter regulatory sequences and T7 polymerase.

Another aspect of the invention pertains to host cells into which a recombinant expression vector of the invention has been introduced. The terms “host cell” and “recombinant host cell” are used interchangeably herein. It is understood that such terms refer not only to the particular subject cell but also to the progeny or potential progeny of such a cell. Because certain modifications may occur in succeeding generations due to either mutation or environmental influences, such progeny may not, in fact, be identical to the parent cell, but are still included within the scope of the term as used herein. A host cell can be any prokaryotic or eukaryotic cell. For example, a nucleic acid of the invention can be expressed in bacterial cells (e.g., E. coli), insect cells, yeast or mammalian cells (such as Chinese hamster ovary cells (CHO) or COS cells). Other suitable host cells are known to those skilled in the art.

Vector DNA can be introduced into prokaryotic or eukaryotic cells via conventional transformation or transfection techniques. As used herein, the terms “transformation” and “transfection” are intended to refer to a variety of art-recognized techniques for introducing foreign nucleic acid (e.g., DNA) into a host cell, including calcium phosphate or calcium chloride co-precipitation, DEAE-dextran-mediated transfection, lipofection, or electroporation. Suitable methods for transforming or transfecting host cells can be found in Sambrook, et al. (supra), and other laboratory manuals.

A host cell of the invention, such as a prokaryotic or eukaryotic host cell in culture, can be used to produce (i.e., express) a polypeptide of the invention. Accordingly, the invention further provides methods for producing a polypeptide using the host cells of the invention. In one embodiment, the method comprises culturing the host cell of the invention (into which a recombinant expression vector encoding a polypeptide of the invention has been introduced) in a suitable medium such that the polypeptide is produced. In another embodiment, the method further comprises isolating the polypeptide from the medium or the host cell.

The host cells of the invention can also be used to produce nonhuman transgenic animals. For example, in one embodiment, a host cell of the invention is a fertilized oocyte or an embryonic stem cell into which a nucleic acid of the invention has been introduced. Such host cells can then be used to create non-human transgenic animals in which exogenous nucleotide sequences have been introduced into their genome or homologous recombinant animals in which endogenous nucleotide sequences have been altered. Such animals are useful for studying the function and/or activity of the nucleotide sequence and polypeptide encoded by the sequence and for identifying and/or evaluating modulators of their activity. As used herein, a “transgenic animal” is a non-human animal, preferably a mammal, more preferably a rodent such as a rat or mouse, in which one or more of the cells of the animal includes a transgene. Other examples of transgenic animals include non-human primates, sheep, dogs, cows, goats, chickens, amphibians, etc. A transgene is exogenous DNA which is integrated into the genome of a cell from which a transgenic animal develops and which remains in the genome of the mature animal, thereby directing the expression of an encoded gene product in one or more cell types or tissues of the transgenic animal. As used herein, an “homologous recombinant animal” is a non-human animal, preferably a mammal, more preferably a mouse, in which an endogenous gene has been altered by homologous recombination between the endogenous gene and an exogenous DNA molecule introduced into a cell of the animal, e.g., an embryonic cell of the animal, prior to development of the animal.

A transgenic animal of the invention can be created by introducing a nucleic acid of the invention into the male pronuclei of a fertilized oocyte, e.g., by microinjection, retroviral infection, and allowing the oocyte to develop in a pseudopregnant female foster animal. The sequence can be introduced as a transgene into the genome of a non-human animal. Intronic sequences and polyadenylation signals can also be included in the transgene to increase the efficiency of expression of the transgene. A tissue-specific regulatory sequence(s) can be operably linked to the transgene to direct expression of a polypeptide in particular cells. Methods for generating transgenic animals via embryo manipulation and microinjection, particularly animals such as mice, have become conventional in the art and are described, for example, in U.S. Pat. Nos. 4,736,866 and 4,870,009, U.S. Pat. No. 4,873,191 and in Hogan, Manipulating the Mouse Embryo (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1986). Similar methods are used for production of other transgenic animals. A transgenic founder animal can be identified based upon the presence of the transgene in its genome and/or expression of mRNA in tissues or cells of the animals. A transgenic founder animal can then be used to breed additional animals carrying the transgene. Moreover, transgenic animals carrying a transgene encoding the transgene can further be bred to other transgenic animals carrying other transgenes.

The invention also relates to the use of the variant and reference gene products to guide efforts to identify the causative mutation for vascular diseases or to identify or synthesize agents useful in the treatment of vascular diseases, e.g., CAD and MI. Amino acids that are essential for function can be identified by methods known in the art, such as site-directed mutagenesis or alanine-scanning mutagenesis (Cunningham et al., Science, 244:1081-1085 (1989)). The latter procedure introduces single alanine mutations at every residue in the molecule. The resulting mutant molecules are then tested for biological activity in vitro, or in vitro activity. Sites that are critical for polypeptide activity can also be determined by structural analysis such as crystallization, nuclear magnetic resonance or photoaffinity labeling (Smith et al., J. Mol. Biol., 224:899-904 (1992); de Vos et al. Science, 255:306-312 (1992)).

Another aspect of the invention pertains to monitoring the influence of agents (e.g., drugs, compounds) on the expression or activity of proteins of the invention in clinical trials. An exemplary method for detecting the presence or absence of proteins or nucleic acids of the invention in a biological sample involves obtaining a biological sample from a test subject and contacting the biological sample with a compound or an agent capable of detecting the protein, or nucleic acid (e.g., mRNA, genomic DNA) that encodes the protein, such that the presence of the protein or nucleic acid is detected in the biological sample. A preferred agent for detecting mRNA or genomic DNA is a labeled nucleic acid probe capable of hybridizing to mRNA or genomic DNA sequences described herein, preferably in an allele-specific manner. The nucleic acid probe can be, for example, a full-length nucleic acid, or a portion thereof, such as an oligonucleotide of at least 15, 30, 50, 100, 250 or 500 nucleotides in length and sufficient to specifically hybridize under stringent conditions to appropriate mRNA or genomic DNA. Other suitable probes for use in the diagnostic assays of the invention are described herein.

The invention also encompasses kits for detecting the presence of proteins or nucleic acid molecules of the invention in a biological sample. For example, the kit can comprise a labeled compound or agent (e.g., nucleic acid probe) capable of detecting protein or mRNA in a biological sample; means for determining the amount of protein or mRNA in the sample; and means for comparing the amount of protein or mRNA in the sample with a standard. The compound or agent can be packaged in a suitable container. The kit can further comprise instructions for using the kit to detect protein or nucleic acid.

The following Examples are offered for the purpose of illustrating the present invention and are not to be construed to limit the scope of this invention. The teachings of all references cited herein are hereby incorporated herein by reference.

EXAMPLES

Identification of Single Nucleotide Polymorphisms

The polymorphisms shown in the Table were identified by resequencing of target sequences from individuals of diverse ethnic and geographic backgrounds by hybridization to probes immobilized to microfabricated arrays. The strategy and principles for design and use of such arrays are generally described in WO 95/11995.

A typical probe array used in this analysis has two groups of four sets of probes that respectively tile both strands of a reference sequence. A first probe set comprises a plurality of probes exhibiting perfect complementarily with one of the reference sequences. Each probe in the first probe set has an interrogation position that corresponds to a nucleotide in the reference sequence. That is, the interrogation position is aligned with the corresponding nucleotide in the reference sequence, when the probe and reference sequence are aligned to maximize complementarily between the two. For each probe in the first set, there are three corresponding probes from three additional probe sets. Thus, there are four probes corresponding to each nucleotide in the reference sequence. The probes from the three additional probe sets are identical to the corresponding probe from the first probe set except at the interrogation position, which occurs in the same position in each of the four corresponding probes from the four probe sets, and is occupied by a different nucleotide in the four probe sets. In the present analysis, probes were 25 nucleotides long. Arrays tiled for multiple different references sequences were included on the same substrate.

Publicly available sequences for a given gene were assembled into Gap4, which can be found on the world wide web at biozentrum.unibas.ch/biocomp/staden/Overview.html. PCR primers covering each exon were designed using Primer 3, which can be found on the world wide web at genome.wi.mit.edu/cgi-bin/primer/primer3.cgi. Primers were not designed in regions where there were sequence discrepancies between reads. Genomic DNA was amplified in at least 50 individuals using 2.5 pmol each primer, 1.5 mM MgCl₂, 100 μM dNTPs, 0.75 μM AmpliTaq GOLD polymerase, and 19 ng DNA in a 15 μl reaction. Reactions were assembled using a PACKARD MultiPROBE robotic pipetting station and then put in MJ 96-well tetrad thermocyclers (96° C. for 10 minutes, followed by 35 cycles of 96° C. for 30 seconds, 59° C. for 2 minutes, and 72° C. for 2 minutes). A subset of the PCR assays for each individual were run on 3% NuSieve gels in 0.5×TBE to confirm that the reaction worked.

For a given DNA, 5 μL (about 50 ng) of each PCR or RT-PCR product were pooled (Final volume=150-200 μl). The products were purified using QiaQuick PCR purification from Qiagen. The samples were eluted once in 35 μl sterile water and 4 μl 10× One-Phor-All buffer (Pharmacia). The pooled samples were digested with 0.2μ DNaseI (Promega) for 10 minutes at 37° C. and then labeled with 0.5 mmols biotin-N-6-ddATP and 15μ Terminal Transferase (GibcoBRL Life Technology) for 60 minutes at 37° C. Both fragmentation and labeling reactions were terminated by incubating the pooled sample for 15 minutes at 100° C.

Low-density DNA chips (Affymetrix, Calif.) were hybridized following the manufacturer's instructions. Briefly, the hybridization cocktail consisted of 3M TMACl, 10 mM Tris pH 7.8, 0.01% Triton X-100, 100 mg/ml herring sperm DNA (Gibco BRL), 200 pM control biotin-labeled oligo. The processed PCR products were denatured for 7 minutes at 100° C. and then added to prewarmed (37° C.) hybridization solution. The chips were hybridized overnight at 44° C. Chips were washed in 1×SSPET and 6×SSPET followed by staining with 2 μg/ml SARPE and 0.5 mg/ml acetylated BSA in 200 μl of 6×SSPET for 8 minutes at room temperature. Chips were scanned using a Molecular Dynamics scanner.

Chip image files were analyzed using Ulysses (Affymetrix, Calif.) which uses four algorithms to identify potential polymorphisms. Candidate polymorphisms were visually inspected and assigned a confidence value: high confidence candidates displayed all three genotypes, while likely candidates showed only two genotypes (homozygous for reference sequence and heterozygous for reference and variant). Some of the candidate polymorphisms were confirmed by ABI sequencing. Identified polymorphisms were compared to several databases to determine if they were novel. Results are shown in the Table.

Association of Thrombospondin Gene Polymorphisms with Vascular Disease

To determine pivotal genes associated with premature coronary artery disease, we analyzed DNA from 347 patients with MI or coronary revascularization before age 40 (men) or 45 (women) and 422 general population controls. Cases were drawn (one per family) from a retrospective collection of sibling pairs with premature CAD. Controls were ascertained through random-digit dialing. Both cases and controls were Caucasian. A complete database of phenotypic and laboratory variables for the affected patients afforded logistic regression to control for age, diabetes, body mass index, gender.

Thrombospondin (TSP) 4 and 1 emerged as important SNPs associated with premature CAD and MI. For CAD, 148 of 347 patients carried at least one copy of the TSP-4 variant compared with 142 of 422 control subjects; adjusted odds ratio 1.47, p=0.01. For premature MI, the association was even stronger: 91 of 187 cases vs. 142 of 422 controls had the variant; adjusted odds ratio 2.08, p=0.0003. The TSP-1 SNP was rare. Nonetheless, homozygosity for the variant allele gave an adjusted odds ratio of 9.5, p=0.04.

		Genbank
		or TIGR	Position			Muta-
Poly	WIAF	Accession	in	Gene	Flanking	tion	Ref	Alt	Ref	Alt
ID	ID	Number	Sequence	Description	Seq	Type	NT	NT	AA	AA

AT3a7	WIAF-13246	U11270	11918	AT3,	CTGCAGGAGT[G/A]GCTGGATGAA	N	G	A	W	*
				antithrombin III
DRD5u22	WIAF-12913	M67439	310	DRD1,	CATCTGGACC[C/T]TGCTGGGCAA	S	C	T	L	L
				dopamine receptor
				D1
DRD5u23	WIAF-12914	M67439	332	DRD1,	GTGCTGGTGT[G/C]CGCAGCCATC	M	G	C	C	S
				dopamine receptor
				D1
DRD5u24	WIAF-12915	M67439	369	DRD1,	TGCGCGCCAA[C/G]ATGACCAACG	M	C	G	N	K
				dopamine receptor
				D1
DRD5u25	WIAF-12916	M67439	522	DRD1,	TGTGCTCCAC[T/C]GCCTCCATCC	S	T	C	T	T
				dopamine receptor
				D1
DRD5u26	WIAF-12917	M67439	953	DRD1,	GCAGAGCACG[C/T]GCAGAGCTGC	M	C	T	A	V
				dopamine receptor
				D1
DRD5u27	WIAF-12918	M67439	635	DRD1,	ATGGTCGGCC[T/C]GGCATGGACC	M	T	C	L	P
				dopamine receptor
				D1
DRD5u2B	WIAF-129l9	M67439	606	DRD1,	GCAAGATGAC[T/C]CAGCGCATGG	S	T	C	T	T
				dopamine receptor
				D1
DRD5u29	WIAF-12920	M67439	845	DRD1,	TCGCTCATCA[G/A]CTTCTACATC	M	G	A	S	N
				dopamine receptor
				D1
DRD5u30	WIAF-12921	M67439	720	DRD1,	CGGGCCGGCT[G/T]GACCTGCCAA	S	G	T	L	L
				dopamine receptor
				D1
DRD5u31	WIAF-12922	M67439	1044	DRD1,	AGACCCTGTC[G/A]GTGATCATGG	S	G	A	S	S
				dopamine receptor
				D1
DRD5u32	WIAF-12923	M67439	766	DRD1,	GGAGGAGGAC[T/G]TTTGGGAGCC	M	T	G	F	V
				dopamine receptor
				D1
DRD5u33	WIAF-12924	N67439	777	DRD1,	TTTCCGAOCC[C/T]GACCTCAATG	S	C	T	P	P
				dopamine receptor
				D1
DRD5u34	WIAF-12925	M67439	786	DRD1,	CCGACGTGAA[T/C]GCACACAACT	M	T	G	N	K
				dopamine receptor
				D1
DRD5u35	WIAF-12926	M67439	881	DRD1,	ACCTACACGC[G/A]CATCTACCGC	M	G	A	R	H
				dopamine receptor
				D1
DRD5u36	WIAF-12927	M67439	1279	DRD1,	GTGCACCCAC[T/G]TCTGCTCCCG	M	T	G	F	V
				dopamine receptor
				D1
DRD5u37	WIAF-12928	M67439	1370	DRD1,	GAAATCGCAG[C/T]TGCCTACATC	M	C	T	A	V
				dopamine receptor
				D1
DRD5u38	WIAF-12929	M67439	1500	DRD1,	ACCCTGTTGC[T/A]GAGTCTGTCT	S	T	A	A	A
				dopamine receptor
				D1
DRD5u39	WIAF-12930	M67439	1338	DRD1,	TCTCCTACAA[C/T]CAAGACATCG	S	C	T	N	N
				dopamine receptor
				D1
DRD5u40	WIAF-12931	M67439	1215	DRD1,	CACTCAACCC[C/A]CTCATCTATG	S	C	A	P	P
				dopamine receptor
				D1
DRD5u41	WIAF-12932	M67439	1242	DRD1,	ACGCCGACTT[T/C]CAGAAGGTGT	S	T	C	P	F
				dopamine receptor
				D1
DRD5u42	WIAF-12933	M67439	1441	DRD1,	CGAGGAGGAC[G/A]GTCCTTTCGA	M	G	A	G	S
				dopamine receptor
				D1
DRD5u43	WIAF-12934	M67439	1460	DRD1,	GATCGCATGT[T/C]CCAGATCTAT	M	T	C	F	S
				dopamine receptor
				D1
DRD5u44	WIAF-12960	M67439	399	DRD1,	TGTCTCTGGC[C/T]GTGTCTGACC	S	C	T	A	A
				dopamine receptor
				D1
DRD5u45	WIAF-12961	M46743	9162	DRD1,	TGCCGCCAGC[C/G]AGcAAcOCCA	S	C	G	G	G
				dopamine receptor
				D1
DRD5u46	WIAF-12962	M67439	195	DRD1,	GGCAGTTCGC[T/G]CTATACCAGC	S	T	G	A	A
				dopamine receptor
				D1
DRD5u47	WIAF-12963	M67439	264	DRD1,	TGGGGCCCTC[A/C]CAGCTCCTCA	S	A	G	S	S
				dopamine receptor
				D1
DRD5u48	WIAF-12964	M61439	465	DRD1,	TGGCCGGTTA[C/T]TGCCCCTTTC	S	C	T	Y	Y
				dopamine receptor
				D1
DRD5u49	WIAF-12965	M67439	511	DRD1,	CTTCGACATC[A/T]TGTGCTCCAC	M	A	T	M	L
				dopamine receptor
				D1
DRD5u50	WIAF-12966	M67439	557	DRD1,	ATCAGCGTGG[A/C]CCCCTACTGG	M	A	G	D	G
				dopamine receptor
				D1
DRD5u51	WIAF-12967	M67439	476	DRD1,	TGGCCCTTTG[C/A]AGCGTTCTGC	M	G	A	G	E
				dopamine receptor
				D1
DRD5u52	WIAF-12968	M67439	1004	DRD1,	AGCCTGCGCG[C/T]TTCCATCAAC	M	C	T	A	V
				dopamine receptor
				D1
DRD5u53	WIAF-12969	M67439	1036	DRD1,	GGTTCTCAAG[A/C]CCCTGTCGGT	M	A	C	T	P
				dopamine receptor
				D1
DRD5u54	WIAF-12970	M67439	859	DRD1,	CTACATCCCC[G/A]TTGCCATCAT	M	G	A	V	I
				dopamine receptor
				D1
DRD5u55	WIAF-12971	M67439	931	DRD1,	GATTTCCTCC[C/T]TGGAGAGGGC	S	C	T	L	L
				dopamine receptor
				D1
G10u1	WIAF-10234	J04111	1308	JUN, v-jun avian	CCCTCAACGC[C/T]TCGTTCCTCC	S	C	T	A	A
				sarcoma virus 17
				oncogene homolog
G10u2	WIAF-10235	J04111	1471	JUN, v-jun avian	GCTGCTCAAG[C/T]TGGCGTCGCC	S	C	T	L	L
				sarcoma virus 17
				oncogene homolog
G10u3	WIAF-10253	J04111	2010	JUN, v-jun avian	TGGAGTCCCA[G/A]GAGCCGATCA	S	G	A	Q	Q
				sarcoma virus 17
				oncogene homolog
G1001u1	WIAF-13746	D26135	993	DGKG, diacyl-	CCCCAGTCGT[C/A]TACCTGAAGG	S	G	A	V	V
				glycerol kinase,
				gamma (90 kD)
G1001u2	WIAF-13764	D26135	2313	DGKG, diacyl-	ATGTGATGAG[A/T]GAGAAACATC	M	A	T	R	S
				glycerol kinase,
				gamma (90 kD)
G1002u1	WIAF-13918	X57206	334	ITPKB, inositol	CCCCAACATC[A/C]GGACAAGCCT	M	A	C	Q	P
				1,4,5-trisphosphate
				3-kinase B
G1002u2	WIAF-13925	X57206	575	ITPKB, inositol	CCAACTCAGC[T/C]TTCCTGCATA	S	T	C	A	A
				1,4,5-trisphosphate
				3-kinase B
G1004u1	WIAF-13567	L36151	1854	PIK4CA, phospha-	GCCGCTCAGA[C/T]TCCGAGGATG	S	C	T	D	D
				tidylinositol 4-
				kinase, catalytic,
				alpha polypeptide
G1006u1	WIAF-12375	HT2690	858	PRKCA, protein	GGTACAAGTT[G/A]CTTAACCAAG	S	G	A	L	L
				kinase C, alpha
G1008u1	WIAF-12397	HT2136	300	PRKCZ, protein	CTGGCCTGCC[A/C]TCTCCCCGAC	S	A	G	P	P
				kinase C, zeta
C1008u2	WIAF-12398	HT2136	246	PRKCZ, protein	AGTGCAGGGA[T/C]GAAGGCCTCA	S	T	C	D	D
				kinase C, zeta
G1008u3	WIAF-12399	HT2136	504	PRKCZ, protein	GCTCCCACCC[C/T]CTCGTCCCCC	S	C	T	G	G
				kinase C, zeta
G1008u4	WIAF-12403	HT2136	807	PRKCZ, protein	AGAAGAATGA[C/T]CAAATTTACG	S	C	T	D	D
				kinase C, zeta
G1008u5	WIAF-12404	HT2136	1514	PRKCZ, protein	GGATTTTCTG[A/T]CATCAACTCC	M	A	T	D	V
				kinase C, zeta
G1008u6	WIAF-12412	HT2136	166	PRKCZ, protein	CAAGTGGGTC[C/A]ACACCGAAGG	M	G	A	D	N
				kinase C, zeta
C1008u7	WIAF-12418	HT2136	560	PRKCZ, protein	TCCCAACAGC[C/T]TCCACTACAC	M	C	T	P	L
				kinase C, zeta
C1009u1	WIAF-12396	L05186	2495	PTK2, PTK2 protein	TCATCAACAA[G/A]ATGAAACTCG	S	G	A	K	K
				tyrosine kinase 2
G1011u1	WIAF-11988	X07876	1250	WNT2, wingless-type	TCCCATCTCA[C/A]CCGCATGACC	M	C	A	T	N
				MMTV integration
				site family member
				2
G1011u2	WIAF-11997	X07876	788	WNT2, wingless-type	CACTATGGGA[T/C]CAAATTTGCC	M	T	C	I	T
				MMTV integration
				site family member
				2
G1011u3	WIAF-12014	X07876	1338	WNT2, wingless-type	TGCACACATG[C/A]AAGGCCCCCA	N	C	A	C	*
				MMTV integration
				site family member
				2
C1011u4	WIAF-13475	X07876	856	WNT2, wingless-type	CCTGATGAAT[C/T]TTCACAACAA	M	C	T	L	F
				MMTV integration
				site family member
				2
C1011u5	WIAF-13476	X07876	958	WNT2, wingless-type	GACATGCTGG[C/T]TGGCCATGGC	S	C	T	L	L
				MMTV integration
				site family member
				2
G1011u6	WIAF-13477	X07876	789	WNT2, wingless-type	ACTATCCGAT[C/T]AAATTTCCCC	S	C	T	I	I
				MMTV integration
				site family member
				2
G1011u7	WIAF-13478	X07876	823	WNT2, wingless-type	TGCAAAGGAA[A/C]GCAAACCAAA	M	A	G	R	G
				MMTV integration
				site family member
				2
G1012u1	WIAF-12408	HT48910	1574	WNT2B, wingless-type	ATACTTGCAA[A/C]GCCCCCAAGA	S	A	G	K	K
				MMTV integration
				site family, member
				2B
G1016a1	WIAF-12125	Z22534	793	ACVR1, activin A	CCCAAGCCGA[A/C]AATGTTCCCG	S	A	G	E	E
				receptor, type I
G1016u2	WIAF-12392	Z22534	373	ACVR1, activin A	CTGGCCAACC[T/C]GTGGACTGCT	S	T	C	A	A
				receptor, type I
G1018u1	WIAF-12413	X74210	1150	ADCY2, adenylate	CAAATTCCGA[C/T]TGCGTATTAA	M	G	T	V	L
				cyclase 2 (brain)
G1019u1	WIAF-12394	U83867	5475	SPTAN1, spectrin,	GCGACCTAAC[T/C]CGCCTCCACA	S	T	C	T	T
				alpha, nonerythro-
				cytic 1 (alpha-
				fodrin)
G1019u2	WIAF-12406	U83867	1223	SPTAN1, spectrin,	GCCCTCATCA[A/G]TGCACATCAC	M	A	G	N	S
				alpha, nonerythro-
				cytic 1 (alpha-
				fodrin)
G1019u3	WIAF-12409	U83867	3555	SPTAN1, spectrin,	CTCAAGCTCT[T/C]ATCCCACACC	S	T	C	L	L
				alpha, nonerythro-
				cytic 1 (alpha-
				fodrin)
G1019u4	WIAF-12415	U83867	3369	SPTAN1, spectrin,	TCCCTCAACC[C/A]AATGAACTAC	S	G	A	A	A
				alpha, nonerythro-
				cytic 1 (alpha-
				fodrin)
C1019u5	WIAF-12417	U83867	5839	SPTAN1, spectrin,	TCACACACAC[T/A]TCACCCTCCA	M	T	A	F	I
				alpha, nonerythro-
				cytic 1 (alpha-
				fodrin)
G1022u1	WIAF-12393	U45945	631	ATP1B2, ATPase,	CATCAATCTT[A/C]CCTCTCCTCC	M	A	G	T	A
				Na+/K+
				transporting, beta
				2 polypeptide
G1022u2	WIAF-12400	U45945	432	ATP1B2, ATPase,	GCCGCCCTGG[G/A]CGCTATTACG	S	G	A	G	G
				Na+/K+
				transporting, beta
				2 polypeptide
G1023u1	WIAF-12401	D89722	395	ARNTL, aryl hydro-	AACATTAAGA[C/C]GTGCCACCAA	M	G	C	G	R
				carbon receptor
				nuclear
				translocator-like
G1023u2	WIAF-12407	D89722	681	ARNTL, aryl hydro-	CTCATAGATC[C/T]AAAAACTGGA	M	C	T	A	V
				carbon receptor
				nuclear
				translocator-like
G1024u1	WIAF-12410	U85946	731	Homo sapiens brain	CATACATTTT[C/T]ACAACTTAAA	M	C	T	S	L
				secretory protein
				hSec10p (HSEC10)
				mRNA, complete cds.
G1027u1	WIAF-12402	L47647	1135	CKB, creatine	TCGAGATGGA[A/G]CAGCGGCTGG	S	A	G	E	E
				kinase, brain
G1027u2	WIAF-12405	L47647	499	CKB, creatine	CCGAGCCCCG[A/C]GCCATCGACA	S	A	C	R	R
				kinase, brain
G103u1	WIAF-10427	HT2269	335	ERCC5, excision	GGGATCCCCA[T/C]CCGAACTCAA	S	T	C	H	H
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G103u2	WIAF-10429	HT2269	1221	ERCC5, excision	CCCTCCTTCT[C/T]CAAGAACTTT	M	C	T	P	S
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G103u3	WIAF-10431	HT2269	1783	ERCC5, excision	TCTCCAACTT[C/C]TACAAATTCT	M	G	C	C	S
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complenientation
				group G (Cockayne
				syndrome))
G103u4	WIAF-10432	HT2269	2077	ERCC5, excision	ACTGAATCTG[C/A]AGGCCAGGAT	M	C	A	A	E
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G103u5	WIAF-10446	HT2269	3338	ERCC5, excision	AATTTGAGCT[A/T]CTTGATAAGG	S	A	T	L	L
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G103u6	WIAF-10447	HT2269	3487	ERCC5, excision	TCAGAATCAT[C/T]TGATGGATCT	M	C	T	S	F
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G103u7	WIAF-10448	HT2269	3507	ERCC5, excision	TTCAAGTGAA[C/G]ATGCTGAAAG	M	C	G	H	D
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G103u8	WIAF-10457	HT2269	1388	ERCC5, excision	CTCTTCACGAE[T/G]CACCAAGATC	M	T	G	D	E
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma-
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G103u9	WIAF-10458	HT2269	1362	ERCC5, excision	CCGGACTCTT[T/C]CAGCCATTAA	M	T	C	S	P
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G103u10	WIAF-10459	HT2269	2357	ERCC5, excision	CTGAGAAAGA[T/C]GCCGAACATT	S	T	C	D	D
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G103u11	WIAF-10462	HT2269	3109	ERCC5, excision	TGGAACAGAA[C/T]GAAGACAGAT	M	C	T	T	M
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G103u12	WIAF-10463	HT2269	3138	ERCC5, excision	GTTTCCTGTA[T/C]TAAAGCAACT	S	T	C	L	L
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G103u14	WIAF-10484	HT2269	3553	ERCC5, excision	AGAACAGCTG[C/T]GAAAGAGCCA	M	C	T	A	V
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G103u15	WIAF-10485	HT2269	1429	ERCC5, excision	CATCTCCACA[C/T]CCGACCGCCA	M	C	T	T	M
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G103a16	WIAF-12097	HT2269	3335	ERCC5, excision	AACAATTTGA[G/T]CTACTTCATA	M	G	T	E	D
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 5 (xeroderma
				pigmentosum,
				complementation
				group G (Cockayne
				syndrome))
G1030u1	WIAF-12411	U07358	203	ZPK, zipper	ACACTTCTGA[C/T]TGCACTCCCG	S	C	T	D	D
				(leucine) protein
				kinase
G1030u2	WIAF-12416	U07358	1806	ZPK, zipper	GCCACCCCAT[G/T]AACCTGGACG	N	G	T	E	*
				(leucine) protein
				kinase
G1031a1	WIAF-12124	U87460	2825	GPR37, G protein-	GAGTCACCAC[C/T]TTCACCTTAT	S	C	T	T	T
				coupled receptor 37
				(endothelin
				receptor type
				B-like)
G1032u1	WIAF-12381	U57911	926	C110RF8, chromosome	ACGTACATCA[A/C]TGCCTCGACG	M	A	C	N	T
				11 open reading
				frame 8
G1033u1	WIAF-12437	M65188	431	GJA1, gap junction	TCTGTACCCA[C/T]ACTCTTCTAC	M	C	T	T	I
				protein, alpha 1,
				43 kD (connexin 43)
G1033u2	WIAF-12438	M65188	169	GJA1, gap junction	ACGCAACATG[G/C]GTGACTGGAG	M	G	C	G	R
				protein, alpha 1,
				43 kD (connexin 43)
G1033u3	WIAF-12439	M65188	467	GJA1, gap junction	TATCTCATGC[C/A]AAAGGAACAG	M	G	A	R	Q
				protein, alpha 1,
				43 kD (connexin 43)
G1033u4	WIAF-12440	M65188	263	GJA1, gap junction	TTCATTTTCC[C/A]AATCCTGCTG	M	C	A	R	Q
				protein, alpha 1,
				43 kD (connexin 43)
G1033u5	WIAF-12441	M65188	218	GJA1, gap junction	CAAGCCTACT[C/T]AACTGCTCGA	M	C	T	S	L
				protein, alpha 1,
				43 kD (connexin 43)
G1033u6	WIAF-12442	M65188	498	GJA1, gap junction	AGAAAGAGGA[A/G]GAACTCAAGC	S	A	G	E	E
				protein, alpha 1,
				43 kD (connexin 43)
G1033u7	WIAF-12465	M65188	550	GJA1, gap junction	GCACTTGAAG[C/A]AGATTGAGAT	M	C	A	Q	K
				protein, alpha 1,
				43 kD (connexin 43)
G1033u8	WIAF-12466	M65188	548	GJA1, gap junction	ATGCACTTGA[A/G]GCACATTGAC	M	A	G	K	R
				protein, alpha 1,
				43 kD (connexin 43)
G1033u9	WIAF-12486	M65188	933	GJA1, gap junction	CCCTGAGCCC[T/C]GCCAAACACT	S	T	C	P	P
				protein, alpha 1,
				43 kD (connexin 43)
G1033u10	WIAF-12487	M65188	990	GJA1, gap junction	CCTCACCAAC[C/T]GCTCCCCTCT	S	C	T	T	T
				protein, alpha 1,
				43 kD (connexin 43)
G1033u11	WIAF-12488	M65188	1034	GJA1, gap junction	AACCTGCTTA[C/A]TCGCGACAGA	M	C	A	T	N
				protein, alpha 1,
				43 kD (connexin 43)
G1033u12	WIAF-12489	M65188	1158	GJA1, gap junction	CTAACTCCCA[T/C]CCACAGCCTT	S	T	C	H	H
				protein, alpha 1,
				43 kD (connexin 43)
G1033u13	WIAF-12490	M65188	1222	GJA1, gap junction	TGGACATGAA[T/C]TACAGCCACT	S	T	C	L	L
				protein, alpha 1,
				43 kD (connexin 43)
G1033u14	WIAF-12491	M65188	1069	GJA1, gap junction	CCGCAATTAC[A/C]ACAAGCAAGC	M	A	G	N	D
				protein, alpha 1,
				43 kD (connexin 43)
G1033u15	WIAF-12492	M65188	1250	GJA1, gap junction	CTCCACCACC[G/A]ACCTTCAAGC	M	G	A	R	Q
				protein, alpha 1,
				43 kD (connexin 43)
G1033u16	WIAF-12496	M65188	423	GJA1, gap junction	TATTTCTCTC[T/C]GTACCCACAC	S	T	C	S	S
				protein, alpha 1,
				43 kD (connexin 43)
G1033u17	WIAF-12503	M65188	880	GJA1, gap junction	CCTTAAGGAT[C/T]GGGTTAACCG	M	C	T	R	W
				protein, alpha 1,
				43 kD (connexin 43)
G1033u18	WIAF-12504	M65188	855	GJA1, gap junction	AACTCTTCTA[T/C]GTTTTCTTCA	S	T	C	Y	Y
				protein, alpha 1,
				43 kD (connexin 43)
G1033u19	WIAF-12505	M65188	576	GJA1, gap junction	AGTTCAAGTA[C/T]GGTATTGAAG	S	C	T	Y	Y
				protein, alpha 1,
				43 kD (connexin 43)
G1033u20	WIAF-12512	M65188	1255	GJA1, gap junction	CCACCCACCT[T/G]CAACCACACC	M	T	G	S	A
				protein, alpha 1,
				43 kD (connexin 43)
G1033u21	WIAF-12513	M65188	1078	GJA1, gap junction	CAACAAGCAA[C/A]CAAGTGACCA	M	G	A	A	T
				protein, alpha 1,
				43 kD (connexin 43)
G1033u22	WIAF-12514	M65188	1097	GJA1, gap junction	CAAAACTCCG[C/G]TAATTACACT	M	C	G	A	G
				protein, alpha 1,
				43 kD (connexin 43)
G1034u1	WIAF-12443	J03544	1201	PYGB, phosphory-	AGACCTGTGC[A/G]TACACCAACC	S	A	G	A	A
				lase, glycogen;
				brain
G1034u2	WIAF-12469	J03544	771	PYGB, phosphory-	GACACCCCAG[T/C]CCCCGGCTAC	M	T	C	V	A
				lase, glycogen;
				brain
G1034u3	WIAF-12470	J03544	1465	PYGB, phosphory-	TCCACTCCGA[C/C]ATCGTCAAAC	M	G	C	E	D
				lase, glycogen;
				brain
G1034u4	WIAF-12471	J03544	1583	PYGB, phosphory-	CCCGCTCCCC[G/A]ATACCATCCT	M	G	A	D	N
				lase, glycogen;
				brain
G1034u5	WIAF-12472	J03544	1774	PYGB, phosphory-	CCATGTTCGA[T/C]GTGCATGTGA	S	T	C	D	D
				lase, glycogen;
				brain
G1034u6	WIAF-12474	J03544	2449	PYGB, phosphory-	AGGTGGACCA[G/A]CTGTACCGGA	S	G	A	Q	Q
				lase, glycogen;
				brain
G1034u7	WIAF-12508	J03544	718	PYGB, phosphory-	CCCCCGACGG[C/T]GTGAAGTGGC	S	C	T	G	G
				lase, glycogen;
				brain
G1035u1	WIAF-12484	U97105	1962	DPYSL2, dihydro-	GCAGAGGAGC[A/G]GCAGACGATC	M	A	G	Q	R
				pyrimidinase-like 2
G1035u2	WIAF-12485	U97105	2842	DPYSL2, dihydro-	ATGACGGACC[T/C]GTGTGTGAAG	S	T	C	P	P
				pyrimidinase-like 2
G1035u3	WIAF-12511	U97105	2062	DPYSL2, dihydro-	CCATCACCAT[C/T]GCCAACCAGA	S	C	T	I	I
				pyrimidinase-like 2
G1036u1	WIAF-12444	D88460	311	WASL, Wiskott-	ACGTGGGGTC[C/T]CTGTTGCTCA	S	C	T	S	S
				Aldrich syndrome
				like
G1038u1	WIAF-12445	HT2746	994	PCTK2, PCTAIRE	TAGAAGAAAG[C/A]TATTGCATCG	M	G	A	V	I
				protein kinase 2
G1039u1	WIAF-12429	HT2747	955	serine/threonine	ATCCAAGAGT[C/T]GCATGTCAGC	M	C	T	R	C
				kinase, PCTAIRE-3
G1039u2	WIAF-12458	HT2747	808	serine/threonine	CACAGAAGAG[A/T]CGTGGCCCGG	M	A	T	T	S
				kinase, PCTAIRE-3
G1041u1	WIAF-12459	X72886	544	H.sapiens TYRO3	CAAGTGGCTG[G/C]CCCTGGAGAG	M	G	C	A	P
				mRNA.
G1041u2	WIAF-12460	X72886	693	H.sapiens TYRO3	TTGGCGGGAA[C/T]CGCCTGAAAC	S	C	T	N	N
				mRNA.
G1041u3	WIAF-12502	X72886	561	H.sapiens TYRO3	AGAGCCTGGC[C/T]GACAACCTGT	S	C	T	A	A
				mRNA.
G1043u1	WIAF-12448	M94055	5481	Human voltage-gated	CTCTGAGTGA[G/A]GATGACTTTG	S	G	A	E	E
				sodium channel
				mRNA, complete cds.
G1043u2	WIAF-12449	M94055	5205	Human voltage-gated	TTGACACCTT[T/C]GGCAACAGCA	S	T	C	F	F
				sodium channel
				mRNA, complete cds.
G1043u3	WIAF-12450	M94055	5224	Human voltage-gated	CATGATCTGC[C/T]TGTTCCAAAT	S	C	T	L	L
				sodium channel
				mRNA, complete cds.
G1043u4	WIAF-12451	M94055	5514	Human voltage-gated	AGGTTTGGGA[C/A]AACTTTCATC	S	C	A	E	E
				sodium channel
				mRNA, complete cds.
G1043u5	WIAF-12452	M94055	5217	Human voltage-gated	CCAACAGCAT[G/C]ATCTCCCTGT	M	G	C	M	I
				sodium channel
				mRNA, complete cds.
G1043u6	WIAF-12453	M94055	5334	Human voltage-gated	CCTCACTTAA[A/G]CCAGACTCTG	S	A	G	K	K
				sodium channel
				mRNA, complete cds.
G1043u7	WIAF-12454	M54055	5424	Human voltage-gated	TGTACATCGC[G/C]GTCATCCTGG	S	G	C	A	A
				sodium channel
				mRNA, complete cds.
G1043u8	WIAF-12455	M94055	5322	Human voltage-gated	ATCACCCTGG[A/C]AGCTCAGTTA	S	A	C	G	G
				sodium channel
				mRNA, complete cds.
G1043u9	WIAF-12456	M94055	1200	Human voltage-gated	ATGGCTACAC[G/A]AGCTTTGACA	S	G	A	T	T
				sodium channel
				mRNA, complete cds.
G1043u10	WIAF-12499	M94055	1170	Human voltage-gated	TCTGTGTGAA[G/T]GCTCGTAGAA	M	G	T	K	N
				sodium channel
				mRNA, complete cds.
G1046a1	WIAF-13187	U50352	267	ACCN1, amiloride-	TCCCACCTGT[C/A]ACCCTCTCTA	S	G	A	V	V
				sensitive cation
				channel 1, neuronal
				(degenerin)
G1046a2	WIAF-13188	U50352	282	ACCN1, amiloride-	TCTGTAACCT[C/g]AATGGCTTCC	S	C	g	L	L
				sensitive cation
				channel 1, neuronal
				(degenerin)
G1046a3	WIAF-13189	U50352	315	ACCN1, amiloride-	TCACCACCAA[C/t]CACCTGTACC	S	C	t	N	N
				sensitive cation
				channel 1, neuronal
				(degenerin)
G1046a4	WIAF-13190	U50352	386	ACCN1, amiloride-	CCCCATCTGG[C/a]TGACCCCTCC	M	C	a	A	D
				sensitive cation
				channel 1, neuronal
				(degenerin)
G1046a5	WIAF-13191	U50352	417	ACCN1, amiloride-	CCCTCCGGCA[C/A]AACCCCAACT	S	G	A	Q	Q
				sensitive cation
				channel 1, neuronal
				(degenerin)
G1048u1	WIAF-12641	HT5174S	3214	REST, RE1-silencing	CAGTCAAACC[G/A]CCTAAGGCAC	S	G	A	A	A
				transcription
				factor
G1048u2	WIAF-12642	HT5174S	3199	REST, RE1-silencing	CAAAGGAAGC[C/G]TTGGCAGTCA	S	C	G	A	A
				transcription
				factor
G1048u3	WIAF-12657	HT5174S	2125	REST, RE1-silencing	CTCCCATCGA[C/T]ACTCCTCAGA	M	G	T	E	D
				transcription
				factor
G1048u4	WIAF-12660	HT5174S	2333	REST, RE1-silencing	CGAACCTCTT[A/C]ACATACACCT	M	A	C	K	Q
				transcription
				factor
G1051u1	WIAF-12431	HT28321	658	SCNN1G, sodium	ATGACACCTC[C/T]GACTGTGCCA	S	C	T	S	S
				channel, non-
				voltage gated 1,
				gamma
G1051u2	WIAF-12434	HT28321	1735	SCNN1G, sodium	AAGCCAAGGA[G/A]TGGTCCGCCT	S	C	A	E	E
				channel, non-
				voltage gated 1,
				gamma
G1051u3	WIAF-12473	HT28321	409	SCNN1G, sodium	AGTCCCTGTA[T/C]GCCTTTCCAC	S	T	C	Y	Y
				channel, non-
				voltage gated 1,
				gamma
G1051u4	WIAF-12475	HT28321	953	SCNN1G, sodium	AGTCATTTTG[T/C]ACATAAACGA	M	T	C	Y	H
				channel, non-
				voltage gated 1,
				gamma
G1051u5	WIAF-12476	HT28321	975	SCNN1G, sodium	GAGCAATACA[A/C]CCCATTCCTC	M	A	G	N	S
				channel, non-
				voltage gated 1,
				gamma
G1051u6	WIAF-12477	HT28321	1192	SCNN1G, sodium	CTGCCTACTC[C/A]CTCCAGATCT	S	G	A	S	S
				channel, non-
				voltage gated 1,
				gamma
G1053a1	WIAF-13192	HT2201	4085	SCN5A, sodium	CGTCCTCTGA[C/A]AGCTCTCTCA	M	G	A	R	K
				channel, voltage-
				gated, type V,
				alpha polypeptide
				(long (electro-
				cardiographic)
				QT syndrome 3)
G1053a2	WIAF-13193	HT2201	5607	SCN5A, sodium	ACTTTCCCCA[C/T]CCCCTGTCTG	S	C	T	D	D
				channel, voltage-
				gated, type V,
				alpha polypeptide
				(long (electro-
				cardiographic)
				QT syndrome 3)
G1053a3	WIAF-13194	HT2201	5828	SCN5A, sodium	GACCCCATCA[C/T]CACCACACTC	M	C	T	T	I
				channel, voltage-
				gated, type V,
				alpha polypeptide
				(long (electro-
				cardiographic)
				QT syndrome 3)
G1053a4	WIAF-13202	HT2201	713	SCN5A, sodium	GCGTTCACTT[T/A]CCTTCCGGAC	M	T	A	F	Y
				channel, voltage-
				gated, type V,
				alpha polypeptide
				(long (electro-
				cardiographic)
				QT syndrome 3)
G1053a5	WIAF-13203	HT2201	6148	SCN5A, sodium	CCACACTGAA[G/T]ATCTCGCCGA	M	G	T	D	Y
				channel, voltage-
				gated, type V,
				alpha polypeptide
				(long (electro-
				cardiographic)
				QT syndrome 3)
G1053a6	WIAF-13204	HT2201	6217	SCN5A, sodium	GCCCTCGCTC[C/T]CCACGACACA	—	G	T	—	—
				channel, voltage-
				gated, type V,
				alpha polypeptide
				(long (electro-
				cardiographic)
				QT syndrome 3)
G1053a7	WIAF-13205	HT2201	6324	SCN5A, sodium	AATCCCCCTC[G/A]CCCCCGCCCA	—	G	A	—	—
				channel, voltage-
				gated, type V,
				alpha polypeptide
				(long (electro-
				cardiographic)
				QT syndrome 3)
G1054u1	WIAF-12419	HT2202	2252	SCN4A, sodium	TTGGCAAGAG[C/T]TACAAGGAGT	S	C	T	S	S
				channel, voltage-
				gated, type IV,
				alpha polypeptide
G1054u2	WIAF-12423	HT2202	4559	SCN4A, sodium	TGGTCATGTT[C/T]ATCTACTCCA	S	C	T	F	F
				channel, voltage-
				gated, type IV,
				alpha polypeptide
G1054u3	WIAF-12424	HT2202	4856	SCN4A, sodium	TCAACATGTA[C/G]ATCGCCATCA	N	C	G	Y	*
				channel, voltage-
				gated, type IV,
				alpha polypeptide
G1054u4	WIAF-12425	HT2202	4777	SCN4A, sodium	GTCAAGGCTC[A/G]CTGCGGCAAC	M	A	G	D	G
				channel, voltage-
				gated, type IV,
				alpha polypeptide
G1054u5	WIAF-12426	HT2202	4863	SCN4A, sodium	GTACATCGCC[A/G]TCATCCTGGA	M	A	G	I	V
				channel, voltage-
				gated, type IV,
				alpha polypeptide
G1054u6	WIAF-12427	HT2202	4566	SCN4A, sodium	GTTCATCTAC[T/G]CCATCTTCGG	M	T	G	S	A
				channel, voltage-
				gated, type IV,
				alpha polypeptide
G1054u7	WIAF-12428	HT2202	4923	SCN4A, sodium	TGGTGAAGAT[G/T]ACTTTGAGAT	M	G	T	D	Y
				channel, voltage-
				gated, type IV,
				alpha polypeptide
G1054u8	WIAF-12446	HT2202	3595	SCN4A, sodium	TTCTGGCTGA[T/C]CTTCAGCATC	M	T	C	I	T
				channel, voltage-
				gated, type IV,
				alpha polypeptide
G1054u9	WIAF-12447	HT2202	4203	SCN4A, sodium	GGAGACAGAC[G/A]ACCAGAGCCA	M	G	A	D	N
				channel, voltage-
				gated, type IV,
				alpha polypeptide
G1054u10	WIAF-12495	HT2202	4811	SCN4A, sodium	TCTGCTTCTT[C/A]TGCAGCTATA	M	C	A	F	L
				channel, voltage-
				gated, type IV,
				alpha polypeptide
G1054u11	WIAF-12497	HT2202	5555	SCN4A, sodium	CAGGGCAGAC[T/G]GTGCGCCCAG	S	T	G	T	T
				channel, voltage-
				gated, type IV,
				alpha polypeptide
G1054u12	WIAF-12498	HT2202	5480	SCN4A, sodium	CACGGGACGC[C/T]GGACCCACTA	S	C	T	A	A
				channel, voltage-
				gated, type IV,
				alpha polypeptide
G1059u1	WIAF-12432	HT33704	112	APLP1, amyloid beta	CGCTGCTGCT[G/A]CCACTATTGC	S	G	A	L	L
				(A4) precursor-like
				protein 1
G1059u2	WIAF-12433	HT33704	140	APLP1, amyloid beta	TCTGCGCGCG[C/T]AGCCCGCCAT	N	C	T	Q	*
				(A4) precursor-like
				protein 1
G1059u3	WIAF-12435	HT33704	1344	APLP1, amyloid beta	CACCATGTGG[C/T]CGCCCTGGAT	M	C	T	A	V
				(A4) precursor-like
				protein 1
G1059u4	WIAF-12457	HT33704	1687	APLP1, amyloid beta	ATCACCGAAA[C/A]CTGAATGCGT	S	C	A	K	K
				(A4) precursor-like
				protein 1
G1059u5	WIAF-12500	HT33704	976	APLP1, amyloid beta	CGTTCCTGAG[A/C]GCCAAGATGG	S	A	G	R	R
				(A4) precursor-like
				protein 1
G1059u6	WIAF-12501	HT33704	1786	APLP1, amyloid beta	GTCAGGCTCT[A/G]TCGGGTCTGC	S	A	G	V	V
				(A4) precursor-like
				protein 1
G1060u1	WIAF-12436	HT1418	1744	APLP2, amyloid beta	CCAAGAAATT[C/C]AAGAGGAAAT	M	C	G	Q	E
				(A4) precursor-like
				protein 2
G1060u2	WIAF-12467	HT1418	2213	APLP2, amyloid beta	ATCACCCTGC[T/C]GATGCTGACC	M	T	G	V	G
				(A4) precursor-like
				protein 2
G1060u3	WIAF-12468	HT1418	2256	APLP2, amyloid beta	GCCACGGGAT[C/T]CTGGAGGTTG	S	C	T	I	I
				(A4) precursor-like
				protein 2
G1066a1	WIAF-13195	HT3538	566	CCKBR, cholecysto-	CTTTGGCACC[G/A]TCATCTGCAA	M	G	A	V	I
				kinin B receptor
G1066a2	WIAF-13196	HT3538	607	CCKBR, cholecysto-	GGGTGTCTGT[G/A]AGTGTGTCCA	S	G	A	V	V
				kinin B receptor
G1066a3	WIAF-13206	HT3538	864	CCKBR, cholecysto-	CTGCTGCTTC[T/A]GCTCTTGTTC	M	T	A	L	Q
				kinin B receptor
G1067u1	WIAF-12478	HT0830	684	KCNA1, potassium	AAACGCTGTG[C/T]ATCATCTGGT	S	C	T	C	C
				voltage-gated
				channel, shaker-
				related subfamily,
				member 1 (episodic
				ataxia with
				myokymia)
G1067u2	WIAF-12479	HT0830	722	KCNA1, potassium	GTGCGCTTCT[T/C]CGCCTGCCCC	M	T	C	F	S
				voltage-gated
				channel, shaker-
				related subfamily,
				member 1 (episodic
				ataxia with myo-
				kymia)
G1067u3	WIAF-12480	HT0830	804	KCNA1, potassium	ATTTCATCAC[C/C]CTCGCCACCG	S	C	G	T	T
				voltage-gated
				channel, shaker-
				related subfamily,
				member 1 (episodic
				ataxia with myo-
				kymia)
G1067u4	WIAF-12509	HT0830	690	KCNA1, potassium	TGTGCATCAT[C/T]TGGTTCTCCT	S	C	T	I	I
				voltage-gated
				channel, shaker-
				related subfamily,
				member 1 (episodic
				ataxia with myo-
				kymia)
G1068u1	WIAF-12493	HT0831	774	KCNA2, potassium	TGAACATCAT[T/A]GACATTGTGG	S	T	A	I	I
				voltage-gated
				channel, shaker-
				related subfamily,
				member 2
G1070a1	WIAF-13197	HT27728	522	KCNJ6, potassium	CACAGTGACC[T/C]GGCTCTTTTT	M	T	C	W	R
				inwardly-rectifying
				channel, subfamily
				J, member 6
G1070a2	WIAF-13201	HT27728	1244	KCNJ6, potassium	CCCTGGAGGA[T/C]GGGTTCTACG	S	T	C	D	D
				inwardly-rectifying
				channel, subfamily
				J, member 6
G1070a3	WIAF-13207	HT27728	707	KCNJ6, potassium	ATAAATGCCC[C/A]GACCGAATTA	S	G	A	P	P
				inwardly-rectifying
				channel, subfamily
				J, member 6
G1071u1	WIAF-12422	HT48672	1534	KCNJ3, potassium	TTCCGGGCAA[C/T]TCAGAACAAA	S	C	T	N	N
				inwardly-rectifying
				channel, subfamily
				J, member 3
G1073u1	WIAF-12461	HT4556	1127	KCNJ1, potassium	CACTGTGCCA[T/C]GTGCCTTTAT	M	T	C	M	T
				inwardly-rectifying
				channel, subfamily
				J, member 1
G1074u1	WIAF-12462	HT27804	289	KCNAB2, potassium	ACCTCTTCGA[T/C]ACACCAGAAG	S	T	C	D	D
				voltage-gated
				channel, shaker-
				related subfamily,
				beta member 2
G1079u1	WIAF-12463	HT27383	1130	potassium channel,	ACCTGGCCGA[T/A]GAGATCCTGT	M	T	A	D	E
				inwardly rectifing
				(GB:D50582)
G1079u2	WIAF-12464	HT27383	1192	potassium channel,	CCTTACTCTG[T/G]GGACTACTCC	M	T	G	V	G
				inwardly rectifing
				(GB:D50582)
G1079u3	WIAF-12481	HT27383	708	potassium channel,	CCTTCCCTCC[A/G]TCTTCATCAA	M	A	G	I	V
				inwardly rectifing
				(GB:D50582)
G1079u4	WIAF-12482	HT27383	779	potassium channel,	CGGTCATCGC[T/C]CTCCCCCACG	S	T	C	A	A
				inwardly rectifing
				(GB:D50582)
G1079u5	WIAF-12483	HT27383	276	potassium channel,	GCACCCTGCC[C/A]ACCCCACCTA	M	G	A	E	K
				inwardly rectifing
				(GB:D50582)
G1079u6	WIAF-12510	HT27383	489	potassium channel,	CTGCCTCATC[C/A]CCTTCCCCCA	M	G	A	A	T
				inwardly rectifing
				(GB:D50582)
G1080u1	WIAF-12536	HT4412	1099	KCNJ4, potassium	TCGACTACTC[A/G]CGTTTTCACA	S	A	G	S	S
				inwardly rectifying
				channel, subfamily
				J, member 4
G1080u2	WIAF-12537	HT4412	1050	KCNJ4, potassium	GGCCACCGCT[T/A]TGAGCCTGTG	M	T	A	F	Y
				inwardly-rectifying
				channel, subfamily
				J, member 4
G1081u1	WIAF-12538	HT27724	1090	KCNJ2, potassium	GGCCACCGCT[A/T]TGAGCCTGTG	M	A	T	Y	F
				inwardly-rectifying
				channel, subfamily
				J, member 2
G1082u1	WIAF-12662	HT28319	768	potassium channel,	CGCGGGTCAC[C/T]GACGAGGGCG	S	C	T	T	T
				inwardly rectify-
				ing, high
				conductance,
				alpha subunit
G1082u2	WIAF-12663	HT28319	854	potassium channel,	CTGGTGTCGC[C/T]CATCACCATC	M	C	T	P	L
				inwardly rectify-
				ing, high
				conductance, alpha
				subunit
G1082u3	WIAF-12679	HT28319	471	potassium channel,	TCTCCATCGA[G/C]ACGCAGACCA	M	G	C	E	D
				inwardly rectify-
				ing, high
				conductance, alpha
				subunit
G1084a1	WIAF-13198	HT0383	2028	KCNB1, potassium	CACTCCCCAG[C/A]AAGACTCCGG	M	C	A	S	R
				voltage-gated
				channel, Shab-
				related subfamily,
				member 1
G1084a2	WIAF-13199	HT0383	2033	KCNB1, potassium	CCCAGCAAGA[C/G]TGGGCGCAGC	M	C	G	T	S
				voltage-gated
				channel, Shab-
				related subfamily,
				member 1
G1084a3	WIAF-13200	HT0383	2321	KCNB1, potassium	GAGTGTGCCA[C/A]GCTTTTGGAC	M	C	A	T	K
				voltage-gated
				channel, Shab-
				related subfamily,
				member 1
G1084a4	WIAF-13208	HT0383	870	KCNB1, potassium	ACAACCCCCA[G/A]CTGGCCCACG	S	C	A	Q	Q
				voltage-gated
				channel, Shab-
				related subfamily,
				member 1
G1088u1	WIAF-12516	HT0522	1503	KCNA5, potassium	TCCTGGGCAA[G/A]ACCTTCCAGC	S	G	A	K	K
				voltage-gated
				channel, shaker-
				related subfamily,
				member 5
G1088u2	WIAF-12519	HT0522	1249	KCNA5, potassium	CGAGCTGCTC[G/A]TGCGCTTCTT	M	G	A	V	M
				voltage-gated
				channel, shaker-
				related subfamily,
				member 5
G1088u3	WIAF-12520	HT0522	973	KCNA5, potassium	CTCTGGGTCC[G/A]CGCGGGCCAT	M	G	A	A	T
				voltage-gated
				channel, shaker-
				related subfamily,
				member 5
G1088u4	WIAF-12521	HT0522	1013	KCNA5, potassium	GTTATCCTCA[T/C]CTCCATCATC	M	T	C	I	T
				voltage-gated
				channel, shaker-
				related subfamily,
				member 5
G1090u1	WIAF-12651	HT1497	1836	KCNA5, potassium	CAACCAGCCA[G/A]TGGAGGAGGC	M	G	A	S	N
				voltage-gated
				channel, shaker-
				related subfamily,
				member 6
G1091u1	WIAF-12714	HT0222	843	KCNA3, potassium	CATCATCTGG[T/C]TCTCCTTCGA	M	T	C	F	L
				voltage-gated
				channel, shaker-
				related subfamily,
				member 3
G1094a1	WIAF-13218	HT27381	1280	KCNJ8, potassium	GTGTATTCTG[T/A]GGATTACTCC	M	T	a	V	E
				inwardly-rectifying
				channel, subfamily
				J, member 8
G1095u1	WIAF-12532	HT2629	765	KCNMA1, potassium	TTCTCTACTT[C/T]GGCTTGCGGT	S	C	T	F	F
				large conductance
				calcium-activated
				channel, subfamily
				M, alpha member 1
G1095u2	WIAF-12533	HT2629	2441	KCNMA1, potassium	GTGGTCTGCA[T/C]CTTTGCCCAC	M	T	C	I	T
				large conductance
				calcium-activated
				channel, subfamily
				M, alpha member 1
G1095u3	WIAF-12534	HT2629	2714	KCNMA1, potassium	GATGATACTT[C/C]GCTCCACCAC	M	C	G	S	W
				large conductance
				calcium-activated
				channel, subfamily
				M, alpha member 1
G1095u4	WIAF-12535	HT2629	2439	KCNMA1, potassium	TCGTGGTCTG[C/T]ATCTTTGGCG	S	C	T	C	C
				large conductance
				calcium-activated
				channel, subfamily
				M, alpha member 1
G1095u5	WIAF-12539	HT2629	3048	KCNMA1, potassium	CACTCATGAG[C/T]GCGACGTACT	S	C	T	S	S
				large conductance
				calcium-activated
				channel, subfamily
				M, alpha member 1
G1095u6	WIAF-12544	HT2629	2352	KCNMA1, potassium	GGATGTTTCA[C/T]TGGTGTGCAC	S	C	T	H	H
				large conductance
				calcium-activated
				channel, subfamily
				M, alpha member 1
G1095u7	WIAF-12545	HT2629	2392	KCNMA1, potassium	CATCCTGACT[C/T]GAAGTGAAGC	N	C	T	R	*
				large conductance
				calcium-activated
				channel, subfamily
				M, alpha member 1
G1095u8	WIAF-12546	HT2629	2295	KCNMA1, potassium	CTGGCAATGA[T/C]CAGATTGACA	S	T	C	D	D
				large conductance
				calcium-activated
				channel, subfamily
				M, alpha member 1
G1095u9	WIAF-12548	HT2629	2949	KCNMA1, potassium	AGTTTTTGGA[C/T]CAAGACGATG	S	C	T	D	D
				large conductance
				calcium-activated
				channel, subfamily
				M, alpha member 1
G1095u10	WIAF-12549	HT2629	2865	KCNMA1, potassium	TGCACGGCAT[G/A]TTACGTCAAC	M	C	A	M	I
				large conductance
				calcium-activated
				channel, subfamily
				M, alpha member 1
G1095u1	WIAF-12547	L26318	930	PRKMB, protein	TGCTGGTAAT[A/T]CATCCATCTA	S	A	T	I	I
				kinase mitogen
				activated 8
				(MAP kinase)
G1098u1	WIAF-12515	L19711	2650	DAG1, dystroglycan	TCTACCTGCA[C/T]ACAGTCATTC	S	C	T	H	H
				1 (dystrophin-
				associated
				glycoprotein 1)
G110u1	WIAF-10385	HT27392	230	meiosis-specific	CAAAGGTATA[C/T]AGATGACAAC	N	C	T	Q	*
				recA homolog,
				HsLim15
G110u2	WIAF-10397	HT27392	1050	meiosis-specific	CCTGAAAATG[A/G]AGCCACCTTC	M	A	G	E	G
				recA homolog,
				HsLim15
G110u3	WIAF-10399	HT27392	674	meiosis-specific	TGAACATCAG[A/G]TGGACCTACT	M	A	G	M	V
				recA homolog,
				HsLim15
G1106u1	WIAF-12647	HT5073	5781	MAP1B, microtubule-	ACTATGAGAA[G/A]ATAGACAGAA	S	C	A	K	K
				associated protein
				1B
G1106u2	WIAF-12648	HT5073	5916	MAP1B, microtubule-	CTGAACAGCG[C/T]GGGTACTCAT	S	C	T	G	G
				associated protein
				1B
G1106u3	WIAF-12650	HT5073	1837	MAP1B, microtubule-	AGACAAGCCA[G/A]TAAAAACAGA	M	G	A	V	I
				associated protein
				1B
G1105u4	WIAF-12653	HT5073	2476	MAP1B, microtubule-	CACCACACCA[G/A]CTGTCATGGC	M	G	A	A	T
				associated protein
				1B
G1106u5	WIAF-12656	HT5073	3913	MAP1B, microtubule-	GCCCAATGAG[A/C]TTAAACTCTC	M	A	G	I	V
				associated protein
				1B
G1106u6	WIAF-12667	HT5073	559	MAP1B, microtubule-	GATTTTCACC[G/A]ATCAAGAGAT	M	G	A	D	N
				associated protein
				1B
G1106u7	WIAF-12668	HT5073	570	MAP1B, microtubule-	ATCAAGAGAT[C/T]CCGGAGTTAC	S	C	T	I	I
				associated protein
				1B
G1106u8	WIAF-12669	HT5073	6175	MAP1B, microtubule-	TACTTCCACA[T/C]ACTCTTACCA	M	T	C	Y	H
				associated protein
				1B
G1106u9	WIAF-12670	HT5073	1215	MAP1B, microtubule-	TCACTCTCCA[C/C]TACCTAAACA	M	G	C	Q	H
				associated protein
				1B
G1106u10	WIAF-12672	HT5073	1821	MAP1B, microtubule-	AGGTAATGGT[G/A]AAAAAAGACA	S	G	A	V	V
				associated protein
				1B
G1106u11	WIAF-12673	HT5073	2727	MAP1B, microtubule-	CTCCTGCCGA[G/T]TCCCCTGATG	M	G	T	E	D
				associated protein
				1B
G1106u12	WIAF-12674	HT5073	2739	MAP1B, microtubule-	CCCCTCATGA[G/A]GGAATCACTA	S	G	A	E	E
				associated protein
				1B
G1106u13	WIAF-12676	HT5073	3643	MAP1B, microtubule-	ACATGCCACT[C/A]ATCCCAAGCA	M	G	A	D	N
				associated protein
				1B
G1106u14	WIAF-12677	HT5073	3609	MAP1B, microtubule-	CACCCCTCAA[C/T]CCATTTTCTG	S	C	T	N	N
				associated protein
				1B
G1106u15	WIAF-12682	HT5073	4752	MAP1B, microtubule-	TTCCACACCC[A/T]ACAACAGATG	S	A	T	p	p
				associated protein
				1B
G1110u1	WIAF-12517	HT1096	1527	myelin associated	GCCCCCTCGT[G/C]CTCACCAGCA	S	G	C	V	V
				glycoprotein
G1110u2	WIAF-12518	HT1096	1678	myelin associated	TGTGCGCCCC[G/T]TGGTCGCCTT	M	G	T	V	L
				glycoprotein
G1110u3	WIAF-12522	HT1096	1271	myelin associated	GCCGTGTCAC[C/T]CCACGATGAT	M	C	T	P L
				glycoprotein
G1113u1	WIAF-12523	HT2242	353	myelin transcrip-	AATTCCGATC[C/T]GATCCTCACC	M	C	T	R	L
				tion factor 1
G1116a1	WIAF-13217	HT28451	417	myelin oligodendro-	CAACCTTATC[G/A]ACACCCTCTC	S	G	A	S	S
				cyte glycoprotein
				(MOG)
G1116a2	WIAF-13219	HT28451	913	myelin oligodendro-	GCAGATCACT[C/G]TTGGCCTCGT	M	C	G	L	V
				cyte glycoprotein
				(MOG)
G1116a3	WIAF-132201	HT28451	922	myelin oligodendro-	TCTTGGCCTC[G/A]TCTTCCTCTG	M	G	A	V	I
				cyte glycoprotein
				(MOG)
G1120u1	WIAF-12525	HT3695	1200	neurofilament,	TAGAGATAGC[T/C]GCTTACAGAA	S	T	C	A	A
				subunit H
G1123u1	WIAF-12542	HT2569	2269	OMG, oligodendro-	CAGCTGCAAC[T/C]CTAACTATTC	S	T	C	T	T
				cyte myelin
				glycoprotein
G1126u1	WIAF-12526	HT28354	626	PSEN2, presenilin 2	GAGCGAAGCA[T/C]GTGATCATGC	S	T	C	H	H
				(Alzheimer disease
				4)
G1126u2	WIAF-12527	HT28354	494	PSEN2, presenilin 2	ATGGAGAGAA[T/C]ACTGCCCAGT	S	T	C	N	N
				(Alzheimer disease
				4)
G1126u3	WIAF-12528	HT28354	434	PSEN2, presenilin 2	TAATGTCGGC[C/T]GAGAGCCCCA	S	C	T	A	A
				(Alzheimer disease
				4)
G1126u4	WIAF-12543	HT28354	550	PSEN2, presenilin 2	GACCCTGACC[G/A]CTATGTCTGT	M	G	A	R	H
				(Alzheimer disease
				4)
G117u1	WIAF-10391	HT27765	156	GTBP, G/T mismatch-	ACTTCTCACC[A/G]GGAGATTTGG	S	A	G	P	P
				binding protein
G117u2	WIAF-10392	HT27765	420	GTBP, G/T mismatch-	AACGTGCAGA[T/C]GAAGCCTTAA	S	T	C	S	S
				binding protein
G117u3	WIAF-10407	HT27765	939	GTBP, G/T mismatch-	CCCACGTTAG[T/C]GGAGGTGGTG	S	T	C	S	S
				binding protein
G117u4	WIAF-10411	HT27765	1622	GTBP, G/T mismatch-
				binding protein	CATTGTTCGA[G/A]ATTTAGGACT	M	G	A	R	K
G117u5	WIAF-10412	HT27765	2405	GTBP, G/T mismatch-	GACAGCAGGG[C/T]TATAATGTAT	M	C	T	A	V
				binding protein
G117u6	WIAF-10413	HT27765	2387	GTBP, G/T mismatch-	AAGAGTCAGA[A/T]CCACCCAGAC	M	A	T	N	I
				binding protein
G125u1	WIAF-10371	HT28632	1999	ATM, ataxia	CAGTAATTTT[C/T]CTCATCTTGT	M	C	T	P	S
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G125u2	WIAF-10372	HT28632	2631	ATM, ataxia	TAATGAATGA[C/A]ATTGCAGATA	M	C	A	D	E
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G125u3	WIAF-10373	HT28632	3084	ATM, ataxia	CAATGGAAGA[T/G]GTTCTTGAAC	M	T	G	D	E
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G125Su5	WIAF-10375	HT28632	4767	ATM, ataxia	CACTTATACC[C/T]CTTGTGTATG	S	C	T	P	P
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G125u6	WIAF-10383	HT28632	8713	ATM, ataxia	ATTCTTGGAT[C/T]CAGCTATTTG	M	C	T	P	S
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G125u7	WIAF-10396	HT28632	1825	ATM, ataxia	CACTTTGGCA[C/G]TGACCACCAG	M	C	G	L	V
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G125u8	WIAF-10398	HT28632	2924	ATM, ataxia	ACTACTGCTC[A/G]GACCAATACT	M	A	G	Q	R
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G125u9	WIAF-10405	HT28632	8967	ATM, ataxia	TTCAACGTGT[C/T]TTCACAAGAT	S	C	T	V	V
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G125u10	WIAF-10408	HT28632	6954	ATM, ataxia	CCAAACACCT[T/C]GTACAACTCT	S	T	C	L	L
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G125u11	WIAF-10409	HT28632	6855	ATM, ataxia	TTCACCACCC[T/C]ATCATCGCTC	S	T	C	P	P
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G125u12	WIAF-10410	HT28632	6801	ATM, ataxia	TATATATTAA[G/T]TGGCAGAAAC	M	G	T	K	N
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G125u13	WIAF-10421	HT28632	335	ATM, ataxia	CATTCAGATT[C/C]CAAACAAGCA	M	C	G	S	C
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G125u14	WIAF-11607	HT28632	3966	ATM, ataxia	TTCCACATCT[C/A]GTCATTAGAA	S	G	A	L	L
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G125a15	WIAF-13130	HT28632	8642	ATM, ataxia	CAGAAATATC[A/C]ACTCTTCATG	M	A	C	E	A
				telangiectasia
				mutated (includes
				complementation
				groups A, C and D)
G136u1	WIAF-10388	HT3337	535	MLH1, mutL	AGGAGAAAAG[C/T]TTTAAAAAAT	M	C	T	A	V
				(E. coli) homolog 1
				(colon cancer, non-
				polyposis type 2)
G136u2	WIAF-10389	HT3337	769	MLH1, mutL	TTCAAAATGA[A/G]TGGTTACATA	M	A	G	N	S
				(E. coli) homolog 1
				(colon cancer, non-
				polyposis type 2)
G144u1	WIAF-11638	HT3625	1129	FOS, v-fos FBJ	CCTCTGCACT[C/T]CGGTCGTCAC	M	C	T	P	S
				murine osteo-
				sarcoma viral
				oncogene homolog
G1461u1	WIAF-12562	HT0329	684	pRB-binding protein	TTGCCAAGAA[C/A]TCCAAGAACC	S	G	A	K	K
G1466u1	WIAF-12571	HT27849	2128	API2, apoptosis	ATGATCCATG[G/C]GTAGAACATG	M	G	C	W	C
				inhibitor 2
G1468u1	WIAF-12563	HT4986	1928	apoptosis	CCACCAGACC[A/T]GACGAGGGGC	S	A	T	P	P
				inhibitor, neuronal
G1468u2	WIAF-12564	HT4986	3057	apoptosis	TTTGCAATTC[C/C]TTCAAGGGAG	M	C	G	L	V
				inhibitor, neuronal
G1472u1	WIAF-12565	HT28478	242	BAK1, BCL2-	GGCACCAGTC[C/T]GGAGAGCCTG	S	C	T	C	C
				antagonist/killer 1
G1472u2	WIAF-12572	HT28478	509	BAK1, BCL2-	TGCACCCCAC[G/A]GCAGAGAATG	S	G	A	T	T
				antagonist/killer 1
G1473u1	WIAF-12568	HT28606	394	CASP6, caspase 6,	GGTGTCAACT[G/C]TTAGCCACGC	M	G	C	V	L
				apoptosis-related
				cysteine protease
G1473u2	WIAF-12576	HT28606	411	CASP6, caspase 6,	ACGCAGATGC[C/T]GATTGCTTTG	S	C	T	A	A
				apoptosis related
				cysteine protease
G1479u1	WIAF-12550	Y09077	711	ATR, ataxia	ACTTTATTAA[T/C]GGTTCTTACT	M	T	C	M	T
				telangiectasis and
				Rad3 related
G1479u2	WIAF-12551	Y09077	4303	ATR, ataxia	TTGCGTATGC[T/C]GATAATAGCC	S	T	C	A	A
				telangiectasia and
				Rad3 related
G1479u3	WIAF-12552	Y09077	1894	ATR, ataxia	ATTCTGATGA[T/C]CCCTGTTTAA	S	T	C	D	D
				telangiectasia and
				Rad3 related
G1479u4	WIAF-12553	Y09077	1855	ATR, ataxia	ATTTATGTGG[T/A]ATGCTCTCAC	S	T	A	G	G
				telangiectasia and
				Rad3 related
G1479u5	WIAF-12558	Y09077	5287	ATR, ataxia	TCATTCATTA[T/C]CATGGTCTAG	S	T	C	Y	Y
				telangiectasia and
				Rad3 related
G1479u6	WIAF-12559	Y09077	5539	ATR, ataxia	CAGCTTTTTA[T/C]GACTCACTGA	S	T	C	Y	Y
				telangiectasia and
				Rad3 related
G1479u7	WIAF-12569	Y09077	1540	ATR, ataxia	ATCCTGTTAT[T/C]GAGATGTTAG	S	T	C	I	I
				telangiectasia and
				Rad3 related
G1479u8	WIAF-12570	Y09077	2521	ATR, ataxia	ATTTAATGGA[A/C]GATCCAGACA	S	A	G	E	E
				telangiectasia and
				Rad3 related
G1482u1	WIAF-12560	HT27870	3176	BLM, Bloom syndrome	AAAATATAAC[G/A]GAATCCAGGA	S	G	A	T	T
G1482u2	WIAF-12561	HT27870	3605	BLM, Bloom syndrome	GAAATAAAGC[C/A]CAAACTGTAC	S	C	A	A	A
G1482u3	WIAF-12573	HT27870	2677	BLM, Bloom syndrome	TATCTATTAC[C/T]GAAAAACCCT	M	C	T	P	L
G1483u1	WIAF-12597	HT1470	1910	MYBL2, v-myb avian	GGATGAGGAT[C/A]TGAAGCTGAT	M	G	A	V	M
				myeloblastosis
				viral oncogene
				homolog-like 2
G14B3u2	WIAF-12610	HT1470	244	MYBL2, v-myb avian	ATGAGGAGGA[C/T]GAGCAGCTGA	S	C	T	D	D
				myeloblastosis
				viral oncogene
				homolog-like 2
G1483u3	WIAF-12611	HT1470	1406	MYBL2, v-myb avian	CACTCAGAAT[A/G]GCACCAGTCT	M	A	G	S	G
				myeloblastosis
				viral oncogene
				homolog-like 2
G1485u1	WIAF-12581	HT1432	1941	BCR, breakpoint	TGGAGATGAG[A/G]AAATGGGTCC	S	A	G	R	R
				cluster region
G1485u2	WIAF-12582	HT1432	3144	BCR, breakpoint	TGACCATCAA[T/C]AAGGAAGATG	S	T	C	N	N
				cluster region
G1485u3	WIAF-12583	HT1432	3777	BCR, breakpoint	ATAACAAGGA[T/C]GTGTCGGTGA	S	T	C	D	D
				cluster region
G1485u4	WIAF-12603	HT1432	2831	BCR, breakpoint	CAGATCAAGA[C/A]TGACATCCAG	M	G	A	S	N
				cluster region
G1485u5	WIAF-12608	HT1432	4217	BCR, breakpoint	ATCCCTGCCC[C/T]GGACAGCAAG	M	C	T	P	L
				cluster region
G1486u1	WIAF-12578	HT33770	1909	BRCA2, breast	ATTGATAATG[G/A]AAGCTGGCCA	M	G	A	G	E
				cancer 2, early
				onset
G1486u2	WIAF-12579	HT33770	3623	BRCA2, breast	AGTTTAGAAA[A/G]CCAAGCTACA	S	A	G	K	K
				cancer 2,
				early onset
G1486u3	WIAF-12586	HT33770	1341	BRCA2, breast	AAATGTAGCA[A/C]ATCAGAAGCC	M	A	C	N	H
				cancer 2, early
				onset
G1486u4	WIAF-12594	HT33770	446	BRCA2, breast	CTTATAATCA[G/A]CTGGCTTCAA	S	G	A	Q	Q
				cancer 2, early
				onset
G1486u5	WIAF-12598	HT33770	3013	BRCA2, breast	ACCATGGTTT[T/C]ATATGGAGAC	M	T	C	L	S
				cancer 2, early
				onset
G1486u6	WIAF-12599	HT33770	3187	BRCA2, breast	GAAAAAAATA[A/T]TGATTACATG	M	A	T	N	I
				cancer 2, early
				onset
G1486u7	WIAF-12604	HT33770	4971	BRCA2, breast	AGCATGTGAG[A/C]CCATTGAGAT	M	A	C	T	P
				cancer 2, early
				onset
G1486u8	WIAF-12607	HT33770	4034	BRCA2, breast	ATGATTCTGT[C/T]GTTTCAATGT	S	C	T	V	V
				cancer 2, early
				onset
G1487u1	WIAF-12584	HT27632	2536	BRCA1, breast	AGTCAGTGTG[C/G]AGCATTTGAA	M	C	G	A	G
				cancer 1, early
				onset
G1487u2	WIAF-12587	HT27632	4697	BRCA1, breast	CATCTCAAGA[G/C]GAGCTCATTA	M	G	C	E	D
				cancer 1, early
				onset
G1487u3	WIAF-12595	HT27632	469	BRCA1, breast	TCTCCTGAAC[A/G]TCTAAAAGAT	M	A	G	H	R
				cancer 1, early
				onset
G1487u4	WIAF-12600	HT27632	3667	BRCA1, breast	AGCGTCCAGA[A/G]AGGAGAGCTT	M	A	G	K	R
				cancer 1, early
				onset
G1487u5	WIAF-12601	HT27632	3537	BRCA1, breast	TATGGGAAGT[A/G]GTCATGCATC	M	A	G	S	G
				cancer 1, early
				onset
G1487u6	WIAF-12602	HT27632	4956	BRCA1, breast	ATCTGCCCAG[A/G]GTCCAGCTGC	M	A	G	S	G
				cancer 1, early
				onset
G1487u7	WIAF-12605	HT27632	2090	BRCA1,breast	AGTACAACCA[A/G]ATGCCAGTCA	S	A	G	Q	Q
				cancer 1, early
				onset
G1487u8	WIAF-12614	HT27632	233	BRCA1,breast	TCTCCACAAA[G/A]TGTGACCACA	S	G	A	K	K
				cancer 1, early
				onset
G1492u1	WIAF-12585	HT3506	3912	cell death-	TCCAGGTCCG[T/C]GGCCTGGAGA	S	T	C	R	R
				associated kinase
G1492u2	WIAF-12593	HT3506	4352	cell death-	TACAACACCA[A/G]TAACGGGGCT	M	A	G	N	S
				associated kinase
G1492u3	WIAF-12606	HT3506	2127	cell death-	GCAATTTGGA[C/T]ATCTCCAACA	S	C	T	D	D
				associated kinase
G1492u4	WIAF-12612	HT3506	1605	cell death-	TCAAATTTCT[C/T]ACTGACAACA	S	C	T	L	L
				associated kinase
G1494u1	WIAF-12589	HT28507	366	cell death-inducing	TTCACCACAC[T/C]TAAGGAGAAC	M	T	C	L	P
				protein Bik
G1495u1	WIAF-12580	HT27803	759	CSE1L, chromosome	TTTCTTCCCT[G/C]ATCCTGATCT	S	G	C	L	L
				segregation 1
				(yeast homolog)-
				like
G1501u1	WIAF-13502	HT1949	1181	MCC, mutated in	CAGCAATGAC[A/C]TTCCCATCGC	M	A	C	I	L
				colorectal cancers
G1501u2	WIAF-13503	HT1949	1753	MCC, mutated in	CAGCTGAGAA[C/T]GCTGCCAAGG	S	C	T	N	N
				colorectal cancers
G1501u3	WIAF-13504	HT1949	2344	MCC, mutated in	TGTCCCTAGC[T/C]GAACTCAGGA	S	T	C	A	A
				colorectal cancers
G1501u4	WIAF-13521	HT1949	445	MCC, mutated in	AGCGAACGAC[G/A]CTTCGCTATG	S	G	A	T	T
				colorectal cancers
G1501u5	WIAF-13522	HT1949	1504	MCC, mutated in	AAAGCAATGC[T/C]GAGAGGATGA	S	T	C	A	A
				colorectal cancers
G1501u6	WIAF-13527	HT1949	2511	MCC, mutated in	TTCGTGAATG[A/G]TCTAAAGCGG	M	A	G	D	G
				colorectal cancers
G1502u1	WIAF-12633	HT1547	870	CCND1, cyclin D1	AGTGTGACCC[A/G]GACTGCCTCC	S	A	G	P	P
				(PRAD1: para-
				thyroid adeno-
				matosis 1)
G1503u1	WIAF-13741	U37022	1151	CDK4, cyclin-	CATGCCAATT[G/A]CATCGTTCAC	M	G	A	C	Y
				dependent kinase 4
G1503u2	WIAF-13742	U37022	1410	CDK4, cyclin-	CTGAAGCCCA[C/T]CAGTTGGGCA	S	C	T	D	D
				dependent kinase 4
G1503u3	WIAF-13743	U37022	1328	CDK4, cyclin-	TATGCAACAC[C/T]TGTGGACATG	M	C	T	P	L
				dependent kinase 4
G1503u4	WIAF-13780	U37022	1194	CDK4, cyclin-	TTCTGGTCAC[A/G]AGTGGTCCAA	S	A	G	T	T
				dependent kinase 4
G1503u5	WIAF-13781	U37022	1443	CDK4, cyclin-	TGATTGGGCT[G/A]CCTCCAGAGG	S	G	A	L	L
				dependent kinase 4
G1503u6	WIAF-13787	U37022	1633	CDK4, cyclin-	CTCTTATCTA[C/T]ATAAGGATGA	M	C	T	H	Y
				dependent kinase 4
G1517u1	WIAF-12618	HT1132	3894	ERBB3, v-erb-b2	CAGACCTCAG[T/C]GCCTCTCTGG	S	T	C	S	S
				avian erythro-
				blastic leukemia
				viral oncogene
				homolog 3
G152u1	WIAF-11608	HT3854	1673	HSPA1L, heat shock	GTGAGTGATG[A/C]AGGTTTCAAG	M	A	C	E	A
				70 kD protein like
				1
G152u2	WIAF-11629	HT3854	1683	HSPA1L, heat shock	AAGGTTTGAA[G/A]GGCAAGATTA	S	G	A	K	K
				70 kD protein like
				1
G152u3	WIAF-11609	HT3854	1478	HSPA1L, heat shock	GTCACAGCCA[C/T]GGACAAGAGC	M	C	T	T	M
				70 kD protein like
				1
G152u4	WIAF-11610	HT3854	1443	HSPA1L, heat shock	TGACGTTTCA[C/T]ATTGATGCCA	S	C	T	D	D
				70 kD protein like
				1
G1520u1	WIAF-12162	HT1175	2211	DNA excision repair	TGACCGTGGA[C/T]GAGGGTGTCC	S	C	T	D	D
				protein ERCC2, 5′
				end
G1520u2	WIAF-12166	HT1175	546	DNA excision repair	CCCACTGCCG[A/C]TTCTATGAGG	S	A	C	R	R
				protein ERCC2, 5′
				end
G1527u1	WIAF-12168	HT0086	577	GSTM2, glutathione	TCATCTCCCG[A/C]TTTGAGGGCT	S	A	C	R	R
				S-transferase M2
				(muscle)
G1527u2	WIAF-12169	HT0086	644	GSTM2, glutathione	ACCTGTGTTC[A/T]CAAAGATGGC	M	A	T	T	S
				S-transferase M2
				(muscle)
G1527u3	WIAF-12171	HT0086	100	GSTM2, glutathione	ACTCAAGCTA[C/T]GAGGAAAAGA	S	C	T	Y	Y
				S-transferase M2
				(muscle)
G1527u4	WIAF-12172	HT0086	41	GSTM2, glutathione	GGGGTACTGG[A/G]ACATCCGCGG	M	A	G	N	D
				S-transferase M2
				(muscle)
G1527u5	WIAF-12173	HT0086	215	GSTM2, glutathione	GATTGATGGG[A/G]CTCACAAGAT	M	A	G	T	A
				S-transferase M2
				(muscle)
G1527u6	WIAF-12194	HT0086	238	GSTM2, glutathione	CCCAGAGCAA[T/C]GCCATCCTGC	S	T	C	N	N
				S-transferase M2
				(muscle)
G1528u1	WIAF-11950	HT1811	529	GSTM3, glutathione	GTATATTTGA[C/G]CCCAAGTGCC	M	C	G	D	E
				S-transferase M3
				(brain)
G1528u2	WIAF-11951	HT1811	674	GSTM3, glutathione	CAACAAGCCT[C/A]TATGCTGAGC	M	G	A	V	I
				S-transferase M3
				(brain)
G1528u3	WIAF-11989	HT1811	572	GSTM3, glutathione	GGCTTTCATG[T/C]GCCGTTTTGA	M	T	G	C	G
				S-transferase M3
				(brain)
G1528u4	WIAF-13470	HT1811	240	GSTM3, glutathione	CAGAGCAATG[C/A]CATCTTGCGC	M	C	A	A	D
				S-transferase M3
				(brain)
G1529u1	WIAF-14146	HT2006	797	GSTM4, glutathione	TGGACGCCTT[C/T]CCAAATCTGA	S	C	T	F	F
				S-transferase M4
G153u1	WIAF-12163	HT3856	1212	HSPA1B, heat shock	TGGGGCTGGA[G/A]ACGGCCGGAG	S	G	A	E	E
				70 kD protein 1
G153u2	WIAF-12182	HT3856	676	HSPA1B, heat shock	GGCCGGGGAC[A/G]CCCACCTGGG	M	A	G	T	A
				70 kD protein 1
G153u3	WIAF-12183	HT3856	1695	HSPA1B, heat shock	TCAGCGAGGC[C/G]GACAAGAAGA	S	C	G	A	A
				70 kD protein 1
G153u4	WIAF-12189	HT3856	330	HSPA1B, heat shock	ACAAGGGGGA[G/C]ACCAAGGCAT	M	G	C	E	D
				70 kD protein 1
G153u5	WIAF-12190	HT3856	1053	HSPA1B, heat shock	AGCTGCTGCA[A/G]GACTTCTTCA	S	A	G	Q	Q
				70 kD protein 1
G1530u1	WIAF-11964	HT3010	673	GSTM5, glutathione	ATTCCTCCGA[G/A]GTCTTTTGTT	M	G	A	G	S
				S-transferase M5
G1530u2	WIAF-11995	HT3010	593	GSTM5, glutathione	GACGCCTTCC[T/C]AAACTTGAAG	M	T	C	L	P
				S-transferase M5
G1530u3	WIAF-13473	HT3010	693	GSTM5, glutathione	TTGGAAAGTC[A/G]GCTACATGGA	S	A	G	S	S
				S-transferase M5
G1533u1	WIAF-13458	HT27460	543	GSTT2, glutathione	CTCTCGGCTA[C/T]GAACTGTTTG	S	C	T	Y	Y
				S-transferase
				theta 2
G1533u2	WIAF-13460	HT27460	417	GSTT2, glutathione	GGACTGCCAT[G/A]GACCAGGCCC	M	G	A	M	I
				S-transferase
				theta 2
G1533u3	WIAF-13461	HT27460	359	GSTT2, glutathione	CAGGTGTTGG[G/A]GCCACTCATT	M	G	A	G	E
				S-transferase
				theta 2
G1533u4	WIAF-13462	HT27460	363	GSTT2, glutathione	TGTTGGGGCC[A/C]CTCATTGGGG	S	A	C	P	P
				S-transferase
				theta 2
G1533u5	WIAF-13463	HT27460	385	GSTT2, glutathione	CCAGGTGCCC[G/A]AGGAGAAGGT	M	G	A	E	K
				S-transferase
				theta 2
G1535u1	WIAF-11952	HT0436	517	HCK, hemopoietic	CCGCGTTGAC[T/C]CTCTGGACAC	M	T	C	S	P
				cells kinase
G1535u2	WIAF-12013	HT0436	783	HCK, hemopoietic	TGGACCACTA[C/T]AAGAAGGGGA	S	C	T	Y	Y
				cells kinase
G1535u3	WIAF-13464	HT0436	357	HCK, hemopoietic	TCATCGTGGT[T/C]GCCCTGTATG	S	T	C	V	V
				cells kinase
G1535u4	WIAF-13465	HT0436	387	HCK, hemopoietic	CCATTCACCA[C/T]GAAGACCTCA	S	C	T	H	H
				cells kinase
G1535u5	WIAF-13466	HT0436	471	HCK, hemopoietic	CCCTGGCCAC[C/G]CGGAAGGACG	S	C	G	T	T
				cells kinase
G1535u6	WIAF-13467	HT0436	240	HCK, hemopoietic	CCAGCGCCAG[C/T]CCACACTCTC	S	C	T	S	S
				cells kinase
G1535u7	WIAF-13468	HT0436	394	HCK, hemopoietic	CCACGAAGAC[C/T]TCAGCTTCCA	M	C	T	L	F
				cells kinase
G1537u1	WIAF-12020	U04045	1514	MSH2, mutS	GTGAATTAAG[A/C]GAAATAATCA	S	A	G	R	R
				(E. coli) homolog 2
				(colon cancer, non-
				polyposis type 1)
G1537u2	WIAF-12044	U04045	599	MSH2, mutS	GACTGTGTGA[A/T]TTCCCTGATA	M	A	T	E	D
				(E. coli) homolog 2
				(colon cancer, non-
				polyposis type 1)
G1537u3	WIAF-12045	U04045	1452	MSH2, mutS	AGATATGGAT[C/T]AGGTGGAAAA	N	C	T	Q	*
				(E. coli) homolog 2
				(colon cancer, non-
				polyposis type 1)
G1537u4	WIAF-12076	U04045	938	MSH2, mutS	GACACTTTGA[A/T]CTGACTACTT	M	A	T	E	D
				(E. coli) homolog 2
				(colon cancer, non-
				polyposis type 1)
G1537u5	WIAF-12077	U04045	1878	MSH2, mutS	TCAGCTAGAT[G/A]CTGTTGTCAG	M	G	A	A	T
				(E. coli) homolog 2
				(colon cancer, non-
				polyposis type 1)
G1543u1	WIAF-13856	J00119	553	MOS, v-mos Moloney	GAGTTTCTGG[G/T]CTGAGCTCAA	M	G	T	A	S
				murine sarcoma
				viral oncogene
				homolog
G1543u2	WIAF-13857	J00119	621	MOS, v-mos Moloney	GCACGCGCAC[G/A]CCCGCAGGGT	S	G	A	T	T
				murine sarcoma
				viral oncogene
				homolog
G1544u1	WIAF-12018	U59464	3821	PTCH, patched	CATCCCGAAT[C/T]CAGGCATCAC	M	C	T	S	F
				(Drosophila)
				homolog
G1544u2	WIAF-12019	U59464	3618	PTCH, patched	GCGTGGTCCG[C/T]TTCGCCATGC	S	C	T	R	R
				(Drosophila)
				homolog
G1544u3	WIAF-12027	U59464	1761	PTCH, patched	ATTTTGCCAT[G/T]GTTCTGCTCA	M	G	T	M	I
				(Drosophila)
				homolog
G1544u4	WIAF-12029	U59464	4074	PTCH, patched	CTGCCATGGG[C/T]AGCTCCGTGC	S	C	T	G	G
				(Drosophila)
				homolog
G1544u5	WIAF-12043	U59464	3845	PTCH, patched	CCCTCGAACC[C/T]GAGACAGCAG	M	C	T	P	L
				(Drosophila)
				homolog
G1544u6	WIAF-12056	U59464	1433	PTCH, patched	CTGCTGGTTG[C/T]ACTGTCAGTG	M	C	T	A	V
				(Drosophila)
				homolog
G1544u7	WIAF-12058	U59464	3298	PTCH, patched	CACCGTTCAC[G/C]TTGCTTTGGC	M	G	C	V	L
				(Drosophila)
				homolog
G1544u8	WIAF-12062	U59464	3986	PTCH, patched	TCTACTGAAG[G/A]GCATTCTGGC	M	G	A	G	E
				(Drosophila)
				homolog
G1544u9	WIAF-13489	U59464	1665	PTCH, patched	CCATCAGCAA[T/C]GTCACAGCCT	S	T	C	N	N
				(Drosophila)
				homolog
G1544u10	WIAF-13490	U59464	2396	PTCH, patched	AAATACTTTT[C/T]TTTCTACAAC	M	C	T	S	F
				(Drosophila)
				homolog
G1544u11	WIAF-13491	U59464	2199	PTCH, patched	GGACACTCTC[A/G]TCTTTTGCTG	S	A	G	S	S
				(Drosophila)
				homolog
G1544u12	WIAF-13492	U59464	2222	PTCH, patched	AAGCACTATG[C/T]TCCTTTCCTC	M	C	T	A	V
				(Drosophila)
				homolog
G1544u13	WIAF-13500	U59464	1686	PTCH, patched	TCTTCATGGC[C/T]GCGTTAATCC	S	C	T	A	A
				(Drosophila)
				homolog
G1545u1	WIAF-12032	HT0473	1835	RAG1, recombina-	GGACATGGAA[G/A]AAGACATCTT	M	G	A	E	K
				tion activating
				gene 1
G1545u2	WIAF-12035	HT0473	2519	RAG1, recombina-	TGACATTGGC[A/G]ATGCAGCTGA	M	A	G	N	D
				tion activating
				gene 1
G1545u3	WIAF-12046	HT0473	3045	RAG1, recombina-	CGGAAAATGA[A/G]TGCCAGGCAG	M	A	G	N	S
				tion activating
				gene 1
G1545u4	WIAF-12047	HT0473	3146	RAG1, recombina-	TCATAATGCA[T/C]TAAAAACCTC	S	T	C	L	L
				tion activating
				gene 1
G1545u5	WIAF-12075	HT0473	2513	RAG1, recombina-	CCACTGTGAC[A/T]TTGGCAATGC	M	A	T	I	F
				tion activating
				gene 1
G1545u6	WIAF-13484	HT0473	1322	RAG1, recombina-	GTCGCTGACT[C/T]GGAGAGCTCA	M	C	T	R	W
				tion activating
				gene 1
G1545u7	WIAF-13494	HT0473	2571	RAG1, recombina-	GAAGTGTATA[A/C]GAATCCCAAT	M	A	G	K	R
				tion activating
				gene 1
G1545u8	WIAF-13498	HT0473	1018	RAG1, recombina-	TTCTGGCTGA[C/A]CCTGTGGAGA	M	C	A	D	E
				tion activating
				gene 1
G1545u9	WIAF-13499	HT0473	2782	RAG1, recombina-	ATCTTTACCT[G/C]AAGATGAAAC S	G	C	L	L
				tion activating
				gene 1
G1548u1	WIAF-12015	HT4999	133	IF127, interferon,	CTCTGCCGTA[G/A]TTTTGCCCCT	M	G	A	V	I
				alpha-inducible
				protein 27
G1548u2	WIAF-13482	HT4999	380	IFI27, interferon,	ATCCTGGGCT[C/T]CATTGGGTCT	M	C	T	S	F
				alpha-inducible
				protein 27
G1548u3	WIAF-13483	HT4999	135	IF127, interferon,	CTGCCGTAGT[T/C]TTGCCCCTGG	S	T	C	V	V
				alpha-inducible
				protein 27
G155u1	WIAF-11634	HT3962	991	CHCl, chromosome	AGCTGGATGT[G/A]CCTGTGGTAA	S	G	A	V	V
				condensation 1
G155u2	WIAF-11635	HT3962	1271	CHCl, chromosome	CGGCTTCGGC[C/T]TCTCCAACTA	M	C	T	L	F
				condensation 1
G155u3	WIAF-11636	HT3962	1192	CHCl, chromosome	GCCGGGGCCA[C/T]GTGAGATTCC	S	C	T	H	H
				condensation 1
G155u4	WIAF-11637	HT3962	1267	CHCl, chromosome	TGTACGGCTT[C/T]GGCCTCTCCA	S	C	T	F	F
				condensation 1
G155u5	WIAF-11649	HT3962	1657	CHCl, chromosome	TGATGGGCAA[A/G]CAGCTGGAGA	S	A	G	K	K
				condensation 1
G1550u1	WIAF-12057	M16038	611	LYN, v-yes-1 Yama-	GCAAAGTCCC[T/G]TTTAACAAAA	M	T	G	L	R
				guchi sarcoma viral
				related oncogene
				homolog
G1550u2	WIAF-12061	M16038	1371	LYN, v-yes-1 Yama-	TGGCATACAT[C/T]GAGCGGAAGA	S	C	T	I	I
				guchi sarcoma viral
				related oncogene
				homolog
G1550u3	WIAF-12080	M16038	1059	LYN, v-yes-1 Yama-	AAAGGCTTGG[C/T]GCTGGGCAGT	S	C	T	G	G
				guchi sarcoma viral
				related oncogene
				homolog
G1550u4	WIAF-12081	M16038	996	LYN, v-yes-1 Yama-	AGCCACAGAA[G/A]CCATGGGATA	S	G	A	K	K
				guchi sarcoma viral
				related oncogene
				homolog
G1552u1	WIAF-12030	HT4578	2355	PMS1, postmeiotic	CCTGCTATTT[A/T]AAAGACTTCT	N	A	T	K	*
				segregation
				increased
				(S. cerevisiae) 1
G1552u2	WIAF-12031	HT4578	2231	PMS1, postmeiotic
				segregation	ACAAAGTTGA[C/T]TTAGAAGAGA	S	C	T	D	D
				increased
				(S. cerevisiae) 1
G1552u3	WIAF-12040	HT4578	617	PMS1, postmeiotic	TCATGAGCTT[T/C]GGTATCCTTA	S	T	C	F	F
				segregation
				increased
				(S. cerevisiae) 1
G1552u4	WIAF-12063	HT4578	1723	PMS1, postmeiotic	TCATGTAACA[A/C]AAAATCAAAT	M	A	G	K	R
				segregation
				increased
				(S. cerevisiae) 1
G1552u5	WIAF-12064	HT4578	1732	PMS1, postmeiotic	AAAAAATCAA[A/G]TGTAATAGAT	M	A	G	N	S
				segregation
				increased
				(S. cerevisiae) 1
G1552u6	WIAF-12065	HT4578	1660	PMS1, postmeiotic	TTACCATGTA[A/G]AGTAAGTAAT	M	A	G	K	R
				segregation
				increased
				(S. cerevisiae) 1
G1552u7	WIAF-12066	HT4578	1975	PMS1, postmeiotic	GAACGATACA[A/G]TAGTCAAATG	M	A	G	N	S
				segregation
				increased
				(S. cerevisiae) 1
G1552u8	WIAF-12067	HT4578	1881	PMS1, postmeiotic	TTTAGAGGAT[G/T]CAACACTACA	M	G	T	A	S
				segregation
				increased
				(S. cerevisiae) 1
G1552u9	WIAF-12068	HT4578	2454	PMS1, postmeiotic	TTTAGACGTT[T/A]TATATAAAAT	M	T	A	L	I
				segregation
				increased
				(S. cerevisiae) 1
G1552u10	WIAF-12069	HT4578	2457	PMS1, postmeiotic	AGACGTTTTA[T/C]ATAAAATGAC	M	T	C	Y	H
				segregation
				increased
				(S. cerevisise) 1
G1552u11	WIAF-12082	HT4578	2557	PMS1, postmeiotic	ATACCAGGAC[T/C]TTCAATTACT	M	T	C	V	A
				segregation
				increased
				(S. cerevisiae) 1
G1552u12	WIAF-12083	HT4578	971	PMS1, postmeiotic
				segregation	TTTTCTTTCT[G/T]AAAATCGATG	S	G	T	L	L
				increased
				(S. cerevisiae) 1
G1554u1	WIAF-12028	HT4161	1500	ELK3, ELK3, ETS-	CTCAGAAATC[C/T]TGATGACCTC	S	C	T	S	S
				domain protein (SRF
				accessory protein
				2) NOTE: Symbol
				and name
				provisional.
G1554u2	WIAF-12059	HT4161	1380	ELK3, ELK3, ETS-	CTGCCAGGCT[G/A]CAAGGGCCAA	S	G	A	L	L
				domain protein (SRF
				accessory protein
				2) NOTE: Symbol
				and name
				provisional.
G1554u3	WIAF-12060	HT4161	1436	ELK3, ELK3, ETS-	CACATGCCAG[T/C]GCCAATCCCC	M	T	C	V	A
				domain protein (SRF
				accessory protein
				2) NOTE: Symbol
				and name
				provisional.
G1562u1	WIAF-12024	HT28220	804	PDCD1, programmed	GGGGCTCAGC[T/C]GACGGCCCTC	S	T	C	A	A
				cell death 1
G1562u2	WIAF-13488	HT28220	644	PDCD1, programmed	GACCCCTCAG[C/T]CGTGCCTCTG	M	C	T	A	V
				cell death 1
G1563u1	WIAF-13493	HT1187	1748	EGFR, epidermal	CCGGAGCCCA[G/A]GGACTGCGTC	M	G	A	R	K
				growth factor
				receptor (avian
				erythroblastic
				leukemia viral
				(v-erb-b) oncogene
				homolog)
G1563u2	WIAF-13497	HT1187	2073	EGFR, epidermal	ACGGATGCAC[T/A]GGGCCAGGTC	S	T	A	T	T
				growth factor
				receptor (avian
				erythroblastic
				leukemia viral
				(v-erb-b) oncogene
				homolog)
G1566u1	WIAF-12016	HT27594	235	PDCD2, programmed	GCGCCGCTGC[C/G]TGGCCGCCCG	M	C	G	P	R
				cell death 2
G1566u2	WIAF-12033	HT27594	904	PDCD2, programmed	TTGGAATTCC[A/G]GGTCATGCCT	M	A	G	Q	R
				cell death 2
G1566u3	WIAF-12041	HT27594	331	PDCD2, programmed	AATCAACTAC[C/T]CAGGAAAAAC	M	C	T	P	L
				cell death 2
G1566u4	WIAF-12071	HT27594	649	PDCD2, programmed	CCTGAGGTTG[T/C]GGAAAAGGAA	M	T	C	V	A
				cell death 2
G1566u5	WIAF-12072	HT27594	633	PDCD2,programmed	AGAAGATGAG[A/T]TTATGCCTGA	M	A	T	I	F
				cell death 2
G1567u1	WIAF-12042	M95936	293	AKT2, v-akt murine	GAGAGGCCGC[G/A]ACCCAACACC	M	G	A	R	Q
				thymoma viral
				oncogene homolog 2
G1572u1	WIAF-12212	HT3998	1894	proto-oncogene c-	TGTTCCAGGA[A/G]TCCAGTATCT	S	A	G	E	E
				abl, tyrosine
				protein kinase,
				alt. transcript 2
G1572u2	WIAF-12233	HT3998	3694	proto-oncogene c-	AGCTTCAGAT[C/T]TGCCCGGCGA	S	C	T	I	I
				abl, tyrosine
				protein kinase,
				alt. transcript 2
G1572u3	WIAF-12234	HT3998	3721	proto-oncogene c-	GCAGTGGTCC[G/A]GCGGCCACTC	S	G	A	P	P
				abl, tyrosine
				protein kinase,
				alt. transcript 2
G1573u1	WIAF-12021	HT0642	343	CBL, Cas-Br-M	TCATGGACAA[G/C]CTGGTGCGGT	M	G	C	K	N
				(murine) ecotropic
				retroviral
				transforming
				sequence
G1573u2	WIAF-12022	HT0642	363	CBL, Cas-Br-M	TTGTGTCAGA[A/T]CCCAAAGCTG	M	A	T	N	I
				(murine) ecotropic
				retroviral
				transforming
				sequence
G1573u3	WIAF-12034	HT0642	2364	CBL, Cas-Br-M	AATATTCAGT[C/T]CCAGGCGCCA	M	C	T	S	P
				(murine) ecotropic
				retroviral
				transforming
				sequence
G1573u4	WIAF-12049	HT0642	387	CBL, Cas-Br-M	CTAAAGAATA[G/A]CCCACCTTAT	M	G	A	S	N
				(murine) ecotropic
				retroviral
				transforming
				sequence
G1573u5	WIAF-12050	HT0642	947	CBL, Cas-Br-M	AACTCATCCT[G/A]GCTACATGGC	M	G	A	G	S
				(murine) ecotropic
				retroviral
				transforming
				sequence
G1573u6	WIAF-12070	HT0642	2740	CBL, Cas-Br-M	TCGAGAACCT[C/T]ATGAGTCAGG	S	C	T	L	L
				(murine) ecotropic
				retroviral
				transforming
				sequence
G1573u7	WIAF-12073	HT0642	661	CBL, Cas-Br-M	TCTTTCCAAG[T/C]GGACTCTTTC	S	T	C	S	S
				(murine) ecotropic
				retroviral
				transforming
				sequence
G1573u8	WIAF-12074	HT0642	2569	CBL, Cas-Br-M	CTCTGGATGG[T/C]GATCCTACAA	S	T	C	G	G
				(murine) ecotropic
				retroviral
				transforming
				sequence
G1573u9	WIAF-13486	HT0642	2006	CBL, Cas-Br-M	CCGGCACTCA[C/T]TTCCATTTTC	M	C	T	L	F
				(murine) ecotropic
				retroviral
				transforming
				sequence
G1574u1	WIAF-12037	HT1508	2493	FES, feline sarcoma
				(Snyder-Theilen)	AGCGGCCCAG[C/T]TTCAGCACCA	S	C	T	S	S
				viral (v-fes)/
				Fujinami avian
				sarcoma (PRCII)
				viral (v-
				fps) oncogene
				homolog
G1574u2	WIAF-12051	HT1508	189	FES, feline sarcoma
				(Snyder-Theilen)	CCCAGCGGGT[C/T]AAGAGTGACA	S	C	T	V	V
				viral (v-fes)/
				Fujinami avian
				sarcoma (pRCII)
				viral (v-
				fps) oncogene
				homolog
G1574u3	WIAF-12052	HT1508	1441	FES, feline sarcoma	GAAGCCCCTG[C/T]ATGAGCAGCT	M	C	T	H	Y
				(Snyder-Theilen)
				viral (v-fes)/
				Fujinami avian
				sarcoma (PRCII)
				viral (v-
				fps) oncogene
				homolog
G1574u4	WIAF-12053	HT1508	2202	FES, feline sarcoma	GAGAGGAAGC[C/T]GATGGGGTCT	S	C	T	A	A
				(Snyder-Theilen)
				viral (v-fes)/
				Fujinami avian
				sarcoma (PRCII)
				viral (v-fps)
				oncogene homolog
G1574u5	WIAF-12054	HT1508	2088	FES, feline sarcoma	CTGCTGGCAT[G/T]GAGTACCTGG	M	G	T	M	I
				(Snyder-Theilen)
				viral (v-fes)/
				Fujinami avian
				sarcoma (PRCII)
				viral (v-fps)
				oncogene homolog
G1574u6	WIAF-12078	HT1508	1577	FES, feline sarcoma	GATGGTCTGC[C/T]CCGGCACTTC	M	C	T	P	L
				(Snyder-Theilen)
				viral (v-fes)/
				Fujinami avian
				sarcoma (PRCII)
				viral (v-fps)
				oncogene homolog
G1574u7	WIAF-13495	HT1508	579	FES, feline sarcoma	GTGACAAGGC[T/C]AAGGACAAGT	S	T	C	A	A
				(Snyder-Theilen)
				viral (v-fes)/
				Fujinami avian
				sarcoma (PRCII)
				viral (v-fps)
				oncogene homolog
G1575u1	WIAF-12079	HT1052	963	FGR, Gardner-	TGGGCACCGG[C/T]TGCTTCGGGG	S	C	T	G	G
				Rasheed feline
				sarcoma viral
				(v-fgr) oncogene
				homolog
G1575u2	WIAF-13487	HT1052	232	FGR, Gardner-	CAGAAGCTAC[G/A]GGGCAGCAGA	M	G	A	G	R
				Rasheed feline
				sarcoma viral
				(v-fgr) oncogene
				homolog
G1585u1	WIAF-12017	HT1675	996	CRK, v-crk avian	TGGATCAACA[G/A]AATCCCGATG	S	G	A	Q	Q
				sarcoma virus CT10
				oncogene homolog
G1585u2	WIAF-12036	HT1675	446	CRK, v-crk avian	ACTACAACGT[T/C]GATAGAACCA	M	T	C	L	S
				sarcoma virus CT10
				oncogene homolog
G1587u1	WIAF-12023	HT0590	1473	proto-oncogene dbl	GGCCAATCCA[A/G]TTTGTGGTAC	S	A	G	Q	Q
G1587u2	WIAF-12025	HT0590	2549	proto-oncogene dbl	GTCCAGGCTT[C/T]TAATGTAGAT	M	C	T	S	F
G1587u3	WIAF-12026	HT0590	2828	proto-oncogene dbl	GCATCACAAT[C/T]TGCAGAAATC	M	C	T	S	F
G1587u4	WIAF-12038	HT0590	982	proto-oncogene dbl	AAATTCTCAG[G/C]AGCTATTATC	M	G	C	E	Q
G1587u5	WIAF-12039	HT0590	2343	proto-oncogene dbl	AACCAATGCA[G/T]CGACACCTTT	M	G	T	Q	H
G1587u6	WIAF-12048	HT0590	683	proto-oncogene dbl	GACACTGAAG[G/A]AGCTGTCAGT	M	G	A	G	E
G1587u7	WIAF-12055	HT0590	2686	proto-oncogene dbl	TTCTCTTCAG[C/T]AGAATGATGA	N	C	T	Q	*
G1587u8	WIAF-13485	HT0590	2136	proto-oncogene dbl	ACTGTGAAGG[T/A]TCTGCTCTGT	S	T	A	G	G
G1587u9	WIAF-13496	HT0590	1566	proto-oncogene dbl	AAAATCAGAG[C/T]AACTTAAAAA	S	C	T	S	S
G159u1	WIAF-11616	HT4209	1059	RAD23B, RAD23	AGTACTGGGG[C/T]TCCTCAGTCT	M	C	T	A	V
				(S. cerevisiae)
				homolog B
G1590u1	WIAF-13897	HT2455	1257	ETS2, v-ets avian	GCCAGTCTCT[C/G]TGCCTCAATA	S	C	G	L	L
				erythroblastosis
				virus E26 oncogene
				homolog 2
G1590u2	WIAF-13913	HT2455	1107	ETS2, v-ets avian	ATTCTGGGAC[T/G]CCCAAAGACC	S	T	G	T	T
				erythroblastosis
				virus E26 oncogene
				homolog 2
G1590u3	WIAF-13914	HT2455	1314	ETS2, v-ets avian	GGAGTGACCC[A/G]GTGGAGCAAG	S	A	G	P	P
				erythroblastosis
				virus E26 oncogene
				homolog 2
G1591u1	WIAF-13924	HT2333	417	HRAS, v-Ha-ras	TCCAGAACCA[T/C]TTTGTGGACG	S	T	C	H	H
				Harvey rat sarcoma
				viral oncogene
				homolog
G1595u1	WIAF-12262	HT33778	1302	proto-oncogene	GCATACCTCA[G/C]TGGCTACTAA	M	G	C	S	T
				1-myc, alt.
				transcript 1
G1597u1	WIAF-12243	HT0410	900	MAS1, MAS1 oncogene	CCATCTTGGT[C/T]GTGAAGATCC	S	C	T	V	V
G150u1	WIAF-11630	HT4247	690	RAD23A, RAD23	AGAGCCAGGT[A/G]TCGGAGCAGC	S	A	G	V	V
				(S. cerevisiae)
				homolog
G1602u1	WIAF-14180	HT1903	1321	proto-oncogene	GTCGCCGGGG[C/A]CCAGCAAATA	M	C	A	P	T
				pim-1
G1604u1	WIAF-12319	HT2788	1182	REL, v-rel avian	CCTCCCAAAG[T/C]GCTGGGATTA	S	T	C	S	S
				reticuloendo-
				theliosis viral
				oncogene homolog
G1609u1	WIAF-12358	HT33646	348	RIPK1, receptor	GACGCACGGT[C/T]TCCCATGACC	S	C	T	V	V
				(TNFRSF) interact-
				ing serine-
				threonine kinase
				1
G161u1	WIAF-11654	HT4251	1522	DNA repair and	TATGATCCAT[C/T]TTAACTGAGG	M	C	T	S	F
				recombination
				homolog RAD52
G1610a1	WIAF-12101	HT27727	501	replication	TGCAACTCCT[G/A]CTATTAAGAC	M	G	A	A	T
				protein Rpa4,
				30 kDa
G1610a2	WIAF-12102	HT27727	554	replication	TACCGTGTAA[C/T]GTGAACCAGC	S	C	T	N	N
				protein Rpa4,
				30 kDa
G1610u3	WIAF-12307	HT27727	450	replication	TTCTGCTGCT[G/A]ATGGAGCGAG	M	G	A	D	N
				protein Rpa4,
				30 kDa
G1610u4	WIAF-12320	HT27727	1037	replication	TGATTCATGA[G/C]TGTCCTCATC	M	G	C	E	D
				protein Rpa4,
				30 kDa
G1610u5	WIAF-12321	HT27727	857	replication	TAGAGGACAT[G/A]AACGAGTTCA	M	G	A	M	I
				protein Rpa4,
				30 kDa
G1610u6	WIAF-12343	HT27727	539	replication	GAATTCAGGA[C/T]GTTGTACCGT	S	C	T	D	D
				protein Rpa4,
				30 kDa
G1630u1	WIAF-12302	HT3563	4312	DCC, deleted in	ACTCATGAAG[C/T]AGCTTAATGC	N	C	T	Q	*
				colorectal
				carcinoma
G1632u1	WIAF-13572	HT27355	742	tumor suppressor,	TTTATGACAT[G/C]AAGCGGGGCT	M	G	C	M	I
				PDGF receptor
				beta-like
G1632u2	WIAF-13584	HT27355	1102	tumor suppressor,	TGGAAGACTT[C/T]GAGACGATTG	S	C	T	F	F
				PDGF receptor
				beta-like
G1632u3	WIAF-13601	HT27355	258	tumor suppressor,	AAGACGCAGT[C/T]TATCATGATG	M	C	T	S	F
				PDGF receptor
				beta-like
G1633u1	WIAF-13957	HT1778	1263	FER, fer (fps/	TTCAGGCAAA[T/C]GAGATCATGT	S	T	C	N	N
				fes related)
				tyrosine kinase
				(phosphoprotein
				NCP94)
G1633u2	WIAF-13958	HT1778	2407	F2R, fer (fps/	TATGTTGTAT[C/T]TCGAGAGTAA	M	C	T	L	F
				fes related)
				tyrosine kinase
				(phosphoprotein
				NCP94)
G1634u1	WIAF-13505	HT3216	1569	ELK1, ELK1, member	TCTCGACCCC[C/T]GTGGTGCTCT	S	C	T	P	P
				of ETS oncogene
				family
G1634u2	WIAF-13858	HT3216	456	ELK1, ELK1, member	GGCTGTGGGG[A/G]CTACGCAAGA	S	A	G	G	G
				oncogene family
G1634u3	WIAF-13859	HT3216	745	ELK1, ELK1, member	AGGCCCAGGC[G/A]GTTTGGCACG	M	G	A	G	S
				of ETS oncogene
				family
G1638u1	WIAF-14172	HT1224	98	uracil-DNA	GCTGGGACCT[G/C]TTCCACAAAT	—	G	C	—	—
				glycosylase
G1643u1	WIAF-13517	HT3751	629	DXS648E, DNA seg-	TACATCCCCA[G/A]TCGTGGCCCT	M	G	A	S	N
				ment on chromosome
				X (unique) 648
				expressed sequence
G1645u1	WIAF-14087	D21089	363	XPC, xeroderma	AAAACCTCAA[G/A]GTTATAAAGG	S	G	A	K	K
				pigmentosum, com-
				plementation group
				C
G1645u2	WIAF-14088	D21089	2166	XPC, xeroderma	TGCATTCCAG[G/A]CACACGTGGC	S	G	A	R	R
				pigmentosum, com-
				plementation group
				C
G1645u3	WIAF-14089	D21089	1580	XPC, xeroderma	GGGAGCCATC[G/A]TAAGGACCCA	M	G	A	R	H
				pigmentosum, com-
				plementation group
				C
G1645u4	WIAF-14090	D21089	1601	XPC, xeroderma	AGCTTGCCAG[T/C]GGCATCCTCA	M	T	C	V	A
				pigmentosum, com-
				plementation group
				C
G1645u5	WIAF-14091	D21089	2920	XPC, xeroderma	CCCATTTGAG[A/C]AGCTGTGAGC	M	A	C	K	Q
				pigmentosum, com-
				plementation group
				C
G1645u6	WIAF-14103	D21089	405	XPC, xeroderma	ATGACCTCAG[G/A]GACTTTCCAA	S	G	A	R	R
				pigmentosum, com-
				plementation group
				C
G1645u7	WIAF-14104	D21089	151	XPC, xeroderma	GGGACGCGAA[C/G]TGCGCAGCCA	M	C	G	L	V
				pigmentosum, com-
				plementation group
				C
G1645u8	WIAF-14105	D21089	2133	XPC, xeroderma	AAGCGGTCTA[C/T]TCCAGGGATT	S	C	T	Y	Y
				pigmentosum, com-
				plementation group
				C
G167u1	WIAF-11632	HT4579	83	PMS2L8, postmeiotic	CCTATTCATC[G/A]GAAGTCAGTC	M	G	A	R	Q
				segregation
				increased 2-like 8
G167u2	WIAF-11633	HT4579	219	PMS2L8, postmeiotic	GAGTGGATCT[T/C]ATTGAAGTTT	S	T	C	L	L
				segregation
				increased 2-like 8
G167u3	WIAF-11644	HT4579	768	PMS2L8, postmeiotic	TGCCCCCTAG[T/C]GACTCCGTGT	S	T	C	S	S
				segregation
				increased 2-like 8
G161u4	WIAF-11622	HT4579	1645	PMS2L8, postmeiotic	GAAAGCGCCT[G/A]AAACTGACGA	M	G	A	E	K
				segregation
				increased 2-like 8
G167u5	WIAF-11645	HT4579	1512	PMS2L8, postmeiotic	ACTCGGGGCA[C/T]GGCAGCACTT	S	C	T	H	H
				segregation
				increased 2-like 8
G167u6	WIAF-11646	HT4579	1619	PMS2L8, postmeiotic	TCGCAGGAAC[A/C]TGTGGACTCT	M	A	G	H	R
				segregation
				increased 2-like 8
G167u7	WIAF-11647	HT4579	1432	PMS2L8, postmeiotic	CGTCCTGAGA[C/T]CTCAGAAAGA	M	C	T	P	S
				segregation
				increased 2-like 8
G167u8	WIAF-11625	HT4579	2490	PMS2L8, postmeiotic	GGACTGCTCT[T/C]AACACAAGCG	S	T	C	L	L
				segregation
				increased 2-like 8
G167u9	WIAF-11619	HT4579	804	PMS2L8, postmeiotic	TGAGCTGTTC[G/C]GATGCTCTGC	S	G	C	S	S
				segregation
				increased 2-like 8
G167u10	WIAF-11623	HT4579	1555	PMS2L8, postmeiotic	CATCCCAGAC[A/G]CGGGCAGTCA	M	A	G	T	A
				segregation
				increased 2-like 8
G167u11	WIAF-11624	HT4575	2364	PMS2L8, postmeiotic	CCTTCGGACC[C/T]CAGGACGTCG	S	C	T	P	P
				segregation
				increased 2-like 8
G167u12	WIAF-11626	HT4579	2348	PMS2L8, postmeiotic	ACTAGTAAAA[A/G]CTGGACCTTC	M	A	G	N	S
				segregation
				increased 2-like 8
G181u1	WIAF-11697	HT48793	311	ERCC4, excision	ATATTTGCGA[C/T]AAGTAGGATA	M	C	T	T	I
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 4
G181u2	WIAF-11698	HT48793	295	ERCC4, excision	CACACAAGGT[G/C]GTGTTATATT	M	G	C	G	R
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 4
G181u3	WIAF-11699	HT48793	234	ERCC4, excision	TTGAACACCT[C/T]CCTCCCCCTC	S	C	T	L	L
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 4
G181u4	WIAF-11704	HT48793	808	ERCC4, excision	TTTGTGGCAC[C/T]AGCTTGGAGC	N	C	T	Q	*
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 4
G181u5	WIAF-11705	HT48793	640	ERCC4, excision	TTCTATGACA[C/T]CTACCATGCT	M	C	T	P	S
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 4
G181u6	WIAF-11670	HT48793	1117	ERCC4, excision	AGAAAGCAAC[C/T]CAAAGTGGGA	M	C	T	P	S
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 4
G185u1	WIAF-11668	HT5122	319	ACVR2B, activin A	TCTGCAACGA[G/A]CGCTTCACTC	S	G	A	E	E
				receptor, type IIB
G185u2	WIAF-11707	HT5122	70	ACVR2B, activin A	AGACACGGGA[G/C]TGCATCTACT	M	G	C	E	D
				receptor, type IIB
G185u3	WIAF-11672	HT5122	812	ACVR2B, activin A	CCTCACGGAT[T/C]ACCTCAAGGG	M	T	C	Y	H
				receptor, type IIB
G185u4	WIAF-13542	X77533	1109	ACVR2B, activin A	GGCTCCTGAG[G/A]TGCTCGAGGG	M	G	A	V	M
				receptor, type IIB
G185u5	WIAF-13558	X77533	997	ACVR2B, activin A	TGCTGAAGAG[C/T]GACCTCACAG	S	C	T	S	S
				receptor, type IIB
G187u1	WIAF-11669	HT97400	183	androgen	CCAGAGACAG[C/T]GCGACCCGGA	M	C	T	R	C
G191u1	WIAF-10176	AF025375	414	CXCR4, chemokine	ACCTGGCCAT[C/T]GTCCACGCCA	S	C	T	I	I
				(C-X-C motif),
				receptor 4 (fusin)
G193u1	WIAF-10178	D29984	231	CCR2, chemokine	AGTGCTTGAC[T/A]GACATTTACC	S	T	A	T	T
				(C-C motif)
				receptor 2
G193u2	WIAF-10179	D29984	190	CCR2, chemokine	CATGCTGGTC[G/A]TCCTCATCTT	M	G	A	V	I
				(C-C motif)
				receptor 2
G194u1	WIAF-10211	D43767	121	SCYA17, small	ACATCCACCC[A/C]GCTCGAGGGA	S	A	C	A	A
				inducible cytokine
				subfamily A
				(Cys-Cys), member
				17
G197u1	WIAF-10167	D50403	1515	NRAMP1, natural	GGTGCTAGTC[T/C]GCGCCATCAA	M	T	C	C	R
				resistance-
				associated
				macrophage protein
				1 (might include
				Leishmaniasis)
G197u2	WIAF-10173	D50403	1629	NRAMP1, natural	CACCTACCTG[G/C]TCTGGACCTG	M	G	C	V	L
				resistance-
				associated
				macrophage protein
				1 (might include
				Leishmaniasis)
G20u1	WIAF-10249	U14722	896	ACVR1B, activin A	CGGTACACAG[T/C]GACAATTGAG	M	T	C	V	A
				receptor, type IB
G20u2	WIAF-10250	U14722	866	ACVR1B, activin A	GAGCACGGGT[C/T]CCTGTTTGAT	M	C	T	S	F
				receptor, type IB
G20u3	WIAF-10251	U14722	1391	ACVR1B, activin A	CAGAGTTATG[A/T]GGCACTGCGG	M	A	T	E	V
				receptor, type IB
G20u4	WIAF-10252	U14722	1236	ACVR1B, activin A	TATATTGGGA[G/C]ATTGCTCGAA	M	G	C	E	D
				receptor, type IB
G20u5	WIAF-10261	U14722	518	ACVR1B, activin A	GAGATGTGTC[T/C]CTCCAAAGAC	M	T	C	L	P
				receptor, type IB
G207a1	WIAF-10516	L25259	866	Human CTLA4	AGCTGTACTT[C/T]CAACAGTTAT	M	C	T	P	S
				counter-receptor
				(B7-2) mRNA,
				complete cds.
G208u1	WIAF-10204	L31581	85	CCR7, chemokine	GGGGAAACCA[A/G]TGAAAAGCGT	M	A	G	M	V
				(C-C motif)
				receptor 7
G211u1	WIAF-10213	M24545	174	SCYA2, small,	TCACCTGCTG[T/C]TATAACTTCA	S	T	C	C	C
				inducible cytokine
				A2 (monocyte
				chemotactic protein
				1, homologous to
				mouse Sig-je)
G214u1	WIAF-10191	M27533	452	CD80, CD80 antigen	TGAAAGAAGT[G/A]GCAACGCTGT	S	G	A	V	V
				(CD28 antigen
				ligand 1, B7-1
				antigen)
G215u1	WIAF-11659	M28393	822	PRF1, perforin 1	GCATCTCTGC[C/T]GAAGCCAAGG	S	C	T	A	A
				(preforming
				protein)
G215u2	WIAF-11723	M28393	159	PRF1, perform 1	TGACCAGCCT[C/T]CGCCGCTCGG	S	C	T	L	L
				(preforming
				protein)
G215u3	WIAF-11724	M28393	96	PRF1, perform 1	CAGAGTGCAA[G/A]CGCAGCCACA	S	G	A	K	K
				(preforming
				protein)
G215u4	WIAF-11725	M28393	1377	PRF1, perform 1	ATAACAACCC[C/T]ATCTGGTCAG	S	C	T	P	P
				(preforming
				protein)
G215u5	WIAF-11726	M28393	1326	PRF1, perform 1	TGAAGCTCTT[C/T]TTTGGTGGCC	S	C	T	F	F
				(preforming
				protein)
G215u6	WIAF-11727	M28393	1076	PRF1, perform 1	CGGCGGGAGG[C/T]ACTGAGGAGG	M	C	T	A	V
				(preforming
				protein)
G217u1	WIAF-11691	M31932	649	FCGR2B, Fc fragment	GCAGCTCTTC[A/C]CCAATGGGGA	S	A	G	S	S
				of IgG, low
				affinity IIb,
				receptor for (CD32)
G217u2	WIAF-11692	M31932	625	FCGR2B, Fc fragment	TCACTGTCCA[A/G]GTGCCCAGCA	S	A	G	Q	Q
				of IgG, low
				affinity IIb,
				receptor for (CD32)
G217u3	WIAF-11712	M31932	332	FCGR2B, Fc fragment	GACTGGCCAG[A/C]CCAGCCTCAG	M	A	C	T	P
				of IgG, low
				affinity IIb,
				receptor for (CD32)
G217u4	WIAF-11713	M31932	101	FCGR2B, Fc fragment	GGCTTCTGCA[G/T]ACAGTCAAGC	M	G	T	D	Y
				of IgG, low
				affinity IIb,
				receptor for (CD32)
G218u1	WIAF-10184	M36712	677	CD8B1, CD8 antigen,	TTTTACAAAT[A/G]AGCAGAGAAT	N	A	G	*	*
				beta polypeptide 1
				(p37)
G218u2	WIAF-10188	M36712	326	CD8B1, CD8 antigen,	GCTGTGTTTC[G/C]GGATGCAAGC	M	G	C	R	P
				beta polypeptide 1
				(p37)
G218u3	WIAF-10189	M36712	196	CD8B1, CD8 antigen,	CAGTAACATG[C/T]GCATCTACTG	M	C	T	R	C
				beta polypeptide 1
				(p37)
G218u4	WIAF-10190	M36712	225	CD8B1, CD8 antigen,	AGCGCCAGGC[A/C]CCGAGCAGTG	S	A	C	A	A
				beta polypeptide 1
				(p37)
G218u5	WIAF-10194	M36712	583	CD8B1, CD8 antigen,	GGTGGCTGGC[G/A]TCCTGGTTCT	M	G	A	V	I
				beta polypeptide 1
				(p37)
G218u6	WIAF-10208	M36712	372	CD8B1, CD8 antigen,	TGAAGCCGGA[A/G]GACAGTGGCA	S	A	G	E	E
				beta polypeptide 1
				(p37)
G218u7	WIAF-10209	M36712	400	CD8B1, CD8 antigen,	CTGCATGATC[G/T]TCGGGAGCCC	M	G	T	V	F
				beta polypeptide 1
				(p37)
G218u8	WIAF-10210	M36712	270	CD8B1, CD8 antigen,	TCTGGGATTC[C/T]GCAAAAGGGA	S	C	T	S	S
				beta polypeptide 1
				(p37)
G218a9	WIAF-10518	M36712	618	CD8B1, CD8 antigen,	GAGTGGCCAT[C/G]CACCTGTGCT	M	C	G	I	M
				beta polypeptide 1
				(p37)
G218a10	WIAF-13223	M36712	556	CD8B1, CD8 antigen,	TTGTAGCCCC[A/G]TCACCCTTGG	M	A	G	I	V
				beta polypeptide 1
				(p37)
G218a11	WIAF-13224	M36712	836	CD8B1, CD8 antigen,	CTGTGTGTGA[T/C]GTGCATGGGA	—	T	C	—	—
				beta polypeptide 1
				(p37)
G22u1	WIAF-10301	U86136	6719	Human telomerase-	GGTGGTAACC[G/A]TCGGGCTAGA	M	G	A	V	I
				associated protein
				TP-1 mRNA, complete
				cds.
G22u2	WIAF-10302	U86136	7537	Human telomerase-	CTGATGGGAT[C/G]CTATGGAACC	M	C	G	I	M
				associated protein
				TP-1 mRNA, complete
				cds.
G22u3	WIAF-10311	U86136	1798	Human telomerase-	ATGATGCCAT[T/C]GATGCCCTCG	S	T	C	I	I
				associated protein
				TP-1 mRNA, complete
				cds.
G22u4	WIAF-10312	U86136	2397	Human telomerase-	CTGTCTCTGG[C/T]TGGCCAAAGG	M	C	T	A	V
				associated protein
				TP-1 mRNA, complete
				cds.
G22u5	WIAF-10313	U86136	3289	Human telomerase-	AGAAAGGGAT[A/C]ACCTGCCGCA	S	A	C	I	I
				associated protein
				TP-1 mRNA, complete
				cds.
G22u6	WIAF-10314	U86136	3242	Human telomerase-	AGAGGCCGCA[T/C]GTCGGATCTC	M	T	C	C	R
				associated protein
				TP-1 mRNA, complete
				cds.
G22u7	WIAF-10315	U86136	4482	Human telomerase-	CCGTTTGCCT[G/A]CCTCGTCCAG	M	G	A	C	Y
				associated protein
				TP-1 mRNA, complete
				cds.
G22u8	WIAF-10316	U86136	4363	Human telomerase-	GTTTGACTGT[G/A]GACCAGCTGC	S	G	A	V	V
				associated protein
				TP-1 mRNA, complete
				cds.
G22u9	WIAF-10317	U86136	4230	Human telomerase-	GTGTCTGAGA[G/A]ACTCCGGACC	M	G	A	R	K
				associated protein
				TP-1 mRNA, complete
				cds.
G22u10	WIAF-10318	U86136	4419	Human telomerase-	GGGACTAAGA[G/C]CTGGGAAGAA	M	G	C	S	T
				associated protein
				TP-1 mRNA, complete
				cds.
G22u11	WIAF-10319	U86136	5269	Human telomerase-	TCTCCGATGA[T/C]ACACTCTTTC	S	T	C	D	D
				associated protein
				TP-1 mRNA, complete
				cds.
G22u12	WIAF-10320	U86136	5015	Human telomerase-	GCTGCTCTCC[C/T]GGAGATGGCA	M	C	T	R	W
				associated protein
				TP-1 mRNA, complete
				cds.
G22u13	WIAF-10321	U86136	5133	Human telomerase-	GTGGCCTTCT[C/T]CACCAATGGG	M	C	T	S	F
				associated protein
				TP-1 mRNA, complete
				cds.
G22u14	WIAF-10322	U86136	7764	Human telomerase-	ACAGCCCTCC[A/G]TGTCCTACCT	M	A	G	H	R
				associated protein
				TP-1 mRNA, complete
				cds.
G22u15	WIAF-10323	U86136	7884	Human telomerase-	TGCCTGGAAC[C/T]TTGCCTGGGC	M	C	T	P	L
				associated protein
				TP-1 mRNA, complete
				cds.
G22u16	WIAF-10324	U86136	7744	Human telomerase-	AGATTCACTC[C/A]GCCTCTGTCA	S	G	A	S	S
				associated protein
				TP-1 mRNA, complete
				cds.
G22u17	WIAF-10337	U86136	1018	Human telomerase-	CCATTGCTGC[T/C]TTCTTGCCGG	S	T	C	A	A
				associated protein
				TP-1 mRNA, complete
				cds.
G22u18	WIAF-10338	U86136	1000	Human telomerase-	TGGCCAATAA[C/A]ATCTTGGCCA	M	C	A	N	K
				associated protein
				TP-1 mRNA, complete
				cds.
G22u19	WIAF-10339	U86136	1182	Human telomerase-	ATGACGGACA[A/G]ATTTGCCCAG	M	A	G	K	R
				associated protein
				TP-1 mRNA, complete
				cds.
G22u20	WIAF-10340	U86136	1939	Human telomerase-	AGCAGCTTCG[T/G]ATGGCAATGA	S	T	G	R	R
				associated protein
				TP-1 mRNA, complete
				cds.
G22u21	WIAF-10341	U86136	2227	Human telomerase-	TCACGAGGGC[G/A]GAGCAGGTGG	S	G	A	A	A
				associated protein
				TP-1 mRNA, complete
				cds.
G22u22	WIAF-10342	U86136	2776	Human telomerase-	GGCGCAGCAT[C/T]CGGCTTTTCA	S	C	T	I	I
				associated protein
				TP-1 mRNA, complete
				cds.
G22u23	WIAF-10343	U86136	2877	Human telomerase-	GCCCCTCACC[C/A]TATCAGCCTT	M	G	A	R	H
				associated protein
				TP-1 mRNA, complete
				cds.
G22u24	WIAF-10344	U86136	3087	Human telomerase-	TCAGGGCGCT[C/T]TGTGACAGAG	M	C	T	S	F
				associated protein
				TP-1 mRNA, complete
				cds.
G22u25	WIAF-10345	U86136	3662	Human telomerase-	CAAGGTGGCA[C/T]CATTAGTCTT	M	C	T	P	S
				associated protein
				TP-1 mRNA, complete
				cds.
G22u26	WIAF-10346	U86136	4762	Human telomerase-	TTTCGAAGTT[C/T]CTTACCAACC	S	C	T	F	F
				associated protein
				TP-1 mRNA, complete
				cds.
G22u27	WIAF-10351	U86136	1737	Human telomerase-	CTCCAGCATG[G/C]GAAGTCGGTG	M	G	C	G	A
				associated protein
				TP-1 mRNA, complete
				cds.
G22u28	WIAF-10352	U86136	3543	Human telomerase-	ACAGTGCAAC[A/G]GCTGATGCTG	M	A	G	Q	R
				associated protein
				TP-1 mRNA, complete
				cds.
G22u29	WIAF-10353	U86136	4232	Human telomerase-	GTCTGAGAGA[C/T]TCCGGACCCT	M	C	T	L	F
				associated protein
				TP-1 mRNA, complete
				cds.
G22u30	WIAF-10354	U86136	4523	Human telomerase-	GGAGGGCCCT[C/T]TGGAGCGCCC	S	C	T	L	L
				associated protein
				TP-1 mRNA, complete
				cds.
G22u31	WIAF-10355	U86136	5333	Human telomerase-	TGGTTGTCGG[G/T]TGCTGCAGAC	M	G	T	V	L
				associated protein
				TP-1 mRNA, complete
				cds.
G22u32	WIAF-10356	U86136	6208	Human telomerase-	AGCTGCTGAC[G/A]CGGCCACACA	S	G	A	T	T
				associated protein
				TP-1 mRNA, complete
				cds.
G22u33	WIAF-10357	U86136	7703	Human telomerase-	TAGTCAGCCA[A/G]CACCACATCT	M	A	G	T	a
				associated protein
				TP-1 mRNA, complete
				cds.
G22u34	WIAF-10360	U86136	3881	Human telomerase-	CATCGATGGG[G/A]CTGATAGGTT	M	G	A	A	T
				associated protein
				TP-1 mRNA, complete
				cds.
G222u1	WIAF-11700	M57230	697	IL6ST, interleukin	TGAGTGGGAT[G/C]GTGGAAGGGA	M	G	C	G	R
				6 signal transducer
				(gp130, oncostatin
				M receptor)
G222u2	WIAF-11701	M57230	708	IL6ST, interleukin	GTGGAAGGGA[A/G]ACACACTTGG	S	A	G	E	E
				6 signal transducer
				(gp130, oncostatin
				M receptor)
G222u3	WIAF-11702	M57230	677	IL6ST, interleukin	GAGGGGAACA[A/G]AATGAGGTGT	M	A	G	K	R
				6 signal transducer
				(gp130, oncostatin
				M receptor)
G222u4	WIAF-11706	M57230	1616	IL6ST, interleukin	AAGAAATATA[T/C]ACTTGAGTGG	M	T	C	I	T
				6 signal transducer
				(gp130, oncostatin
				M receptor)
G222u5	WIAF-11667	M57230	1444	IL6ST, interleukin	TGATCGCTAT[C/G]TAGCAACCCT	M	C	G	L	V
				6 signal transducer
				(gp130, oncostatin
				M receptor)
G222u6	WIAF-11708	M57230	981	IL6ST, interleukin	TCTTAAAATT[G/C]ACATGGACCA	M	G	C	L	F
				6 signal transducer
				(gp130, oncostatin
				M receptor)
G226u1	WIAF-11714	M85079	869	TGFBR2, transform-	CACTGGGAGT[T/C]GCCATATCTG	S	T	C	V	V
				ing growth factor,
				beta receptor II
				(70-80 kD)
G226u2	WIAF-11715	H85079	1749	TGFBR2, transform-	ACATTATCAC[C/T]CTCCATTTCC	M	C	T	P	S
				ing growth factor,
				beta receptor II
				(70-80 kD)
G226u3	WIAF-11716	M85079	1601	TGFBR2, transform-	TCCCAACTCC[A/C]ACATACATCC	S	A	G	A	A
				ing growth factor,
				beta receptor II
				(70-80 kD)
G226u4	WIAF-11721	H85079	1256	TGFBR2, transform-	TACTCCACTT[C/C]CTCACCCCTC	M	C	G	F	L
				ing growth factor,
				beta receptor II
				(70-80 kD)
G226u5	WIAF-11722	M85079	1502	TGFBR2, transform-	TCCTCAACAA[C/T]CACCTAACCT	S	C	T	N	N
				ing growth factor,
				beta receptor II
				(70-80 kD)
G226u6	WIAF-11671	M85079	888	TGFBR2, transform-	TCTCATCATC[A/C]TCTTCTACTC	M	A	C	I	L
				ing growth factor,
				beta receptor II
				(70-80 kD)
G226u7	WIAF-11674	M85079	1425	TGFBR2, transform-	CCTCCACAGT[G/A]ATCACACTCC	M	G	A	D	N
				ing growth factor,
				beta receptor II
				(70-80 kD)
G227u1	WIAF-10197	M86511	685	CD14, CD14 antigen	CCTGTCTGAC[A/G]ATCCTGGACT	M	A	G	N	D
G227u2	WIAF-10212	M86511	497	CD14, CD14 antigen	GAAGCCACAG[G/A]ACTTGCACTT	M	G	A	G	E
G2278u1	WIAF-14117	AF034611	959	CUBN, cubilin	ACATAAATAA[T/C]CGCCCCTGTT	S	T	C	N	N
				(intrinsic factor-
				cobalamn receptor)
G2278u2	WIAF-14118	AF034611	781	CUBN, cubilin	CCGTGGATGT[C/T]TTCACCCAAC	M	C	T	S	F
				(intrinsic factor-
				cobalain receptor)
G2278u3	WIAF-14119	AF034611	641	CUBN, cubilin	CTCAGACGTA[C/T]CCACCCCAGT	S	C	T	Y	Y
				(intrinsic factor-
				cobalamin receptor)
G2278u4	WIAF-14121	AF034611	1185	CUBN, cubilin	TCCTTATCCG[C/A]CAAATGCATG	M	C	A	P	T
				(intrinsic factor-
				cobalamin receptor)
G2278u5	WIAF-14133	AF034611	1532	CUBN, cubilin	TCTGCGTTAT[C/G]AAAACTGAAA	M	C	G	I	M
				(intrinsic factor
				cobalamin receptor)
G2278u6	WIAF-14134	AF034611	2208	CUBN, cubilin	GCCTTTCACT[C/T]ACACCAGGCA	M	C	T	H	Y
				(intrinsic factor
				cobalamin receptor)
G228u1	WIAF-10199	U00672	586	IL10RA, interleukin	CCAACGTCCC[G/A]CCAAACTTCA	S	G	A	P	P
				10 receptor, alpha
G228u2	WIAF-10200	U00672	731	IL10RA, interleukin	AGAGCAGTGC[A/G]TCTCCCTCAC	M	A	G	I	V
				10 receptor, alpha
G2280u1	WIAF-13970	AJ001515	1747	RYR3, ryanodine	CAGGTATCTT[G/A]GAAGTTTTGC	S	G	A	L	L
				receptor 3
G2280u2	WIAF-13974	AJ001515	8593	RYR3, ryanodine	TAGAAGCCAT[T/C]GTCAGCAGTG	S	T	C	I	I
				receptor 3
G2282u1	WIAF-12694	D00726	263	FECH,	ACATGGGAGG[C/T]CCTGAAACTG	S	C	T	G	G
				ferrochelatase
				(protoporphyria)
G2282u2	WIAF-12695	D00726	514	FECH,	TACTATATTG[G/A]ATTTCGGTAC	M	G	A	G	E
				ferrochelatase
				(protoporphyria)
G2285u1	WIAF-12688	D16611	673	CPO, copropor-	AGAAGACGCT[G/A]TCCATTTTCA	M	G	A	V	I
				phyrinogen oxidase
				(coproporphyria,
				harderoporphyria)
G2285u2	WIAF-12689	D16611	783	CPO, copropor-	ATCGTGGAGA[G/A]CGGCGGGGCA	S	G	A	E	E
				phyrinogen oxidase
				(coproporphyria,
				harderoporphyria)
G2287u1	WIAF-12687	D28472	502	PTGER4, prosta-	GGGCCTCACG[C/T]TCTTTGCAGT	M	C	T	L	F
				glandin E receptor
				4 (subtype EP4)
G2287u2	WIAF-12691	D28472	1309	PTGER4, prosta-	TGAAAATGGC[C/T]TTGGAGGCAG	M	C	T	L	F
				glandin E receptor
				4 (subtype EP4)
G2287u3	WIAF-12707	D28472	243	PTGER4, prosta-	AGGAGACGAC[C/T]TTCTACACGC	S	C	T	T	T
				glandin E receptor
				4 (subtype EP4)
G2287u4	WIAF-12710	D28472	1342	PTGER4, prosta-	GGTGTGCCTG[G/A]CATGGGCCTG	M	G	A	G	D
				glandin E receptor
				4 (subtype EP4)
G229u1	WIAF-10185	U16752	202	SDF1, stromal cell-	CATGTTGCCA[G/A]AGCCAACCTC	M	G	A	R	K
				derived factor 1
G2295u1	WIAF-12727	D89079	613	LTB4R, leukotriene	CTATGTCTGC[G/C]GAGTCAGCAT	M	G	C	G	R
				b4 receptor (chemo-
				kine receptor-like
				1)
G2295u2	WIAF-1272B	D89079	1248	LTB4R, leukotriene	AGGGCACGGG[T/C]TCCGAGGCGT	S	T	C	G	G
				b4 receptor (chemo-
				kine receptor-like
				1)
G2295u3	WIAF-12753	D89079	1348	LTB4R, leukotriene	CCTCACTGCC[T/G]CCAGCCCTCT	M	T	G	S	A
				b4 receptor (chemo-
				kine receptor-like
				1)
G230u1	WIAF-10201	U31628	627	IL15RA, interleukin	ACAGCCAAGA[A/C]CTGGGAACTC	M	A	C	N	T
				15 receptor, alpha
				alpha
G2300u1	WIAF-12735	J02959	102	LTA4H, leukotriene	ACCTGCACCT[C/T]CGCTGCACGC	S	G	T	L	L
				A4 hydrolase
G2300u2	WIAF-12738	J02959	1380	LTA4H, leukotriene	CCTGGCTCTA[C/T]TCTCCTGGAC	S	C	T	Y	Y
				A4 hydrolase
G2302u1	WIAF-12741	J03037	627	CA2, carbonic	TCCTGAATCC[C/T]TGGATTACTG	S	C	T	L	L
				anhydrase II
G2302u2	WIAF-12742	J03037	819	CA2, carbonic	GCCACTGAAG[A/G]ACAGGCAAAT	M	A	G	N	D
				anhydrase II
G2303u1	WIAF-12751	J03571	304	ALOX5, arachidonate	CGCTGAAGAC[G/A]CCCCACGGGG	S	G	A	T	T
				5-lipoxygenase
G2303u2	WIAF-12752	J03571	794	ALOX5, arachidonate	AGAGCTGCCC[G/A]AGAAGCTCCC	M	G	A	E	K
				5-lipoxygenase
G2304u1	WIAF-12772	J03575	840	PDHA1, pyruvate	TCCGAGAGGC[A/C]ACAAGGTTTG	S	A	G	A	A
				dehydrogenase
				(lipoamide) alpha 1
G2304u2	WIAF-12779	J03575	1044	PDHA1, pyruvate	CCAGTGTGGA[A/C]GAACTAAAGG	M	A	C	E	D
				dehydrogenase
				(lipoamide) alpha 1
G2305u1	WIAF-12763	J03576	456	PDHB, pyruvate	TCTTCAGGGG[A/G]CCCAATGGTG	S	A	G	G	G
				debydrogenase
				(lipoamide) beta
G2305u2	WIAF-12764	J03576	650	PDHB, pyruvate	GTTCCTTTTG[A/C]ATTTCTCCCG	M	A	C	E	A
				dehydrogenase
				(lipoamide) beta
G231u1	WIAF-10202	U32324	734	IL11RA, interleukin	CCAGGGCCTG[C/T]GGGTAGAGTC	M	C	T	R	W
				11 receptor, alpha
G2312u1	WIAF-12762	J05096	3726	ATP1A2, ATPase,	TCAAGAACCA[C/T]ACAGAGATCG	S	C	T	H	H
				Na+/K+
				transporting,
				alpha 2 (+)
				polypeptide
G2313u1	WIAF-12760	J05200	6141	RYR1, ryanodine	TGCAATTCAA[A/G]GATGGTACAG	S	A	G	K	K
				receptor 1
				(skeletal)
G2313u2	WIAF-12767	J05200	3048	RYR1, ryanodine	CGGCGCAGAC[A/G]ACACTGGTGG	S	A	G	T	T
				receptor 1
				(skeletal)
G2313u3	WIAF-12768	J05200	3084	RYR1, ryanodine	ATGGCCACAA[C/T]GTGTGGGCCC	S	C	T	N	N
				receptor 1
				(skeletal)
G2313u4	WIAF-12777	J05200	5667	RYR1, ryanodine	GCATCTTTGG[C/T]GATGAGGATG	S	C	T	G	G
				receptor 1
				(skeletal)
G2313u5	WIAF-12780	J05200	6600	RYR1, ryanodine	GCTCGCTGCT[C/T]ATCGTGCAGA	S	C	T	L	L
				receptor 1
				(skeletal)
G2313u6	WIAF-12781	J05200	7191	RYR1, ryanodine	AGCCTGAGTG[C/T]TTCGHACCCG	S	C	T	C	C
				receptor 1
				(skeletal)
G2313u7	WIAF-12782	J05200	7602	RYR1, ryanodine	ACCACAAGGC[G/A]TCCATGGTGC	S	G	A	A	A
				receptor 1
				(skeletal)
G2313u8	WIAF-12784	J05200	9288	RYR1, ryanodine	CAGACGCCCC[A/G]GCTCTGGTCA	S	A	G	P	P
				receptor 1
				(skeletal)
G2313u9	WIAF-12786	J05200	13690	RYR1, ryanodine	TCCAAAGAAG[G/A]AGGAAGCTGG	M	G	A	E	K
				receptor 1
				(skeletal)
G2313u10	WIAF-12789	J05200	3147	RYR1, ryanodine	ACATCCCAGC[G/A]CGCCCAAACC	S	G	A	A	A
				receptor 1
				(skeletal)
G23144u1	WIAF-12771	J05272	1920	IMPDH1, IMP	TGAAGATCGC[A/G]CAGGGTGTCT	S	A	G	A	A
				(inosine mono-
				phosphate)
				dehydrogenase 1
G2319u1	WIAF-12814	K03191	651	CYP1A1, cytochrome	CCCCTACAGG[T/C]ATGTGGTGGT	M	T	C	Y	H
				P450, subfamily I
				(aromatic compound
				inducible), poly-
				peptide 1
G232u1	WIAF-11657	U58917	1490	Homo sapiens IL,-17	TGAACATGAT[C/T]CTCCCGGACT	S	C	T	I	I
				receptor mRNA,
				complete cds.
G232u2	WIAF-11677	U58917	1293	Homo sapiens IL-17	GCAGGCCATC[T/C]CGGAGGCAGG	M	T	C	S	P
				receptor mRNA,
				complete cds.
G232u3	WIAF-11658	U58917	1132	Homo sapiens IL-17	GGCCTGCCTG[C/T]GGCTCACCTG	M	C	T	A	V
				receptor mRNA,
				complete cds.
G232u4	WIAF-11679	U58917	905	Homo sapiens IL-17	GCAGCTGCCT[C/T]AATGACTGCC	S	C	T	L	L
				receptor mRNA,
				complete cds.
G232u5	WIAF-11682	U58917	1794	Homo sapiens IL-17	GTTCGAATGTE[G/T]AGAACCTCTA	N	G	T	E	*
				receptor mRNA,
				complete cds.
G232u7	WIAF-11660	U58917	743	Homo sapiens IL-17	TGACCAGTTT[T/C]CCGCACATGG	S	T	C	F	F
				receptor mRNA,
				complete cds.
G2322u1	WIAF-12853	L01406	1316	GHRHR, growth	CTGACATCTA[T/C]GTGCTAGGCT	M	T	C	M	T
				hormone releasing
				hormone receptor
G2328u1	WIAF-12845	L20316	1285	GCGR, glucagon	TGCGGGCACG[G/C]CAGATGCACC	S	G	C	R	R
				receptor
G2329u1	WIAF-12850	L22214	713	ADORA1, adenosine	TGCTGGCAAT[T/C]GCTGTGGACC	S	T	C	I	I
				A1 receptor
G2329u2	WIAF-12851	L22214	716	ADORA1, adenosine	TGGCAATTGC[T/G]GTGGACCGCT	S	T	G	A	A
				A1 receptor
G2335a1	WIAF-12136	L32961	265	ABAT, 4-amino-	CCTAGATCTC[A/G]GGAGTTAATG	M	A	G	Q	R
				butyrate amino-
				transferase
G2335a2	WIAF-12137	L32961	407	ABAT, 4-amino-	TCTCCTCTGT[T/C]CCCATAGGTT	S	T	C	V	V
				butyrate amino-
				transferase
G2335u3	WIAF-12838	L32961	365	ABAT, 4-amino-	TTGATGTGGA[C/T]GGCAACCGAA	S	C	T	D	D
				butyrate amino-
				transferase
G2335u4	WIAF-12839	L32961	583	ABAT, 4-amino-	ATCACCATGG[C/T]CTGCGGCTCC	M	C	T	A	V
				butyrate amino-
				transferase
G2335u5	WIAF-12841	L32961	1082	ABAT, 4-amino-	TGGACGAGGT[C/A]CAGACCGGAG	S	C	A	V	V
				butyrate amino-
				transferase
G2335u6	WIAF-12852	L32961	227	ABAT, 4-amino-	ATTATGATGG[C/A]CCTCTGATGA	S	G	A	G	G
				butyrate amino-
				transferase
G2337u1	WIAF-13577	L34820	149	ALDH5A1, aldehyde	TGTTCTCGAA[A/C]GAATGCCAAG	M	A	G	K	R
				dehydrogenase 5
				family, member A1
				(succinate-semi-
				aldehyde
				dehydrogenase)
G2342a1	WIAF-12138	M12530	1602	TF, transferrin	GCCTAAACCT[G/C]TGTGAACCCA	S	G	C	L	L
G2342a2	WIAF-12139	M12530	1795	TF, transferrin	TACCAGGAAA[C/T]CTGTGGAGGA	M	C	T	P	S
G2346u1	WIAF-12829	M13928	234	ALAD, aminolevuli-	TGGCCAGGTA[T/C]GGTGTGAAGC	S	T	C	Y	Y
				nate, delta-,
				dehydratase
G2346u2	WIAF-12830	M13928	529	ALAD, aminolevuli-	TGAGGTGGCA[T/C]TGGCGTATGC	S	T	C	L	L
				nate, delta-,
				dehydratase
G2346u3	WIAF-12843	M13928	480	ALAD, aminolevuli-	TGAGTGAAAA[C/T]GGAGCATTCC	S	C	T	N	N
				nate, delta-,
				dehydratase
G2348u1	WIAF-12835	M14016	621	UROD, uroporphyrino-	CTCTGGTCCC[A/G]TATCTGGTAG	S	A	G	P	P
				gen decarboxylase
G235u1	WIAF-11678	U83171	100	SCYA22, small	CAGGCCCCTA[C/T]GGCGCCAACA	S	C	T	Y	Y
				inducible cytokine
				subfamily A (Cys-
				Cys), member 22
G2363a1	WIAF-10519	M37435	596	CSF1, colony	GACAAGGACT[G/T]GAATATTTTC	M	G	T	W	L
				stimulating factor
				1 (macrophage)
G2363a2	WIAF-13225	M37435	498	CSF1, colony	AAGAGCATGA[C/T]AAGGCCTGCG	S	C	T	D	D
				stimulating factor
				1 (macrophage)
G2363a3	WIAF-13226	M37435	712	CSF1, colony	CAGTGACCCG[G/T]CCTCTGTCTC	M	G	T	A	S
				stimulating factor
				1 (macrophage)
G2369u1	WIAF-12854	M30773	857	PPP3R1, protein	TTGATTTGCA[C/T]AATTCTCGTT	S	C	T	D	D
				phosphatase 3
				(formerly 2B),
				regulatory subunit
				B (19 kD), alpha
				isoform
				(calcineurin B,
				type I)
G2369u2	WIAF-12855	M30773	1274	PPP3R1, protein	ATGTGTGACT[C/T]TTATCAGAGA	-	C	T	-	-
				phosphatase 3
				(formerly 25),
				regulatory subunit
				B (19 kD), alpha
				isoform
				(calcineurin B,
				type I)
G237u1	WIAF-11662	U86358	311	SCYA25, small	CACCACAACA[T/C]GCAGACCTTC	M	T	C	M	T
				inducible cytokine
				subfamily A (Cys-
				Cys), member 25
G237u2	WIAF-11680	U86358	134	SCYA25, small	GTGCTCCGGC[G/A]CGCCTGGACT	M	G	A	R	H
				inducible cytokine
				subfamily A (Cys-
				Cys), member 25
G237u3	WIAF-11681	U86358	133	SCYA25, small	TGTGCTCCGG[C/T]GCGCCTGGAC	M	C	T	R	C
				inducible cytokine
				subfamily A (Cys-
				Cys), member 25
G237u5	WIAF-11661	U86358	302	SCYA25, small	GCAAAGCTCC[A/G]CCACAACATG	M	A	G	H	R
				inducible cytokine
				subfamily A (Cys-
				Cys), member 25
G237u6	WIAF-11663	U86358	378	SCYA25, small	AGTTATCATC[A/C]TCCAAGTTTA	S	A	G	S	S
				inducible cytokine
				subfamily A (Cys-
				Cys), member 25
G2373u1	WIAF-12870	M36035	500	BZRP, benzo-	GCTGGCCTTC[G/A]CGACCACACT	M	G	A	A	T
				diazapine receptor
				(peripheral)
G2376u1	WIAF-13025	M57414	979	TACR2, tachykinin	CTGCTGCCCA[T/C]GGGTCACACC	M	T	C	W	R
				receptor 2
G238u1	WIAF-10177	X01394	239	TNF, tumor necrosis	GCTCCAGGCG[G/T]TGCTTGTTCC	S	G	T	R	R
				factor (TNF super-
				family, member 2)
G2381u1	WIAF-12894	M59941	730	CSF2RB, colony	CAGAGGTTTG[C/T]TGGGACTCCC	S	C	T	C	C
				stimulating factor
				2 receptor, beta,
				low-affinity
				(granulocyte-
				macrophage)
G2381u2	WIAF-12896	M59941	1306	CSF2RB, colony	GGATCTGGAG[C/T]GAGTGGAGTG	S	C	T	S	S
				stimulating factor
				2 receptor, beta,
				low-affinity
				(granulocyte-
				macrophage)
G2381u3	WIAF-12900	M59941	1972	CSF2RB, colony	CGATGGGACCC[G/A]GGACAGGCCG	S	G	A	P	P
				stimulating factor
				2 receptor, beta,
				low-affinity
				(granulocyte-
				macrophage)
G2381u4	WIAF-12901	M59941	1982	CSF2RB, colony	GGGACAGGCC[G/A]TGGAACTGGA	M	G	A	V	M
				stimulating factor
				2 receptor, beta,
				low-affinity
				(granulocyte-
				macrophage)
G2381u5	WIAF-12942	M59941	773	CSF2RB, colony	CCAGAACCTG[G/C]AGTGCTTCTT	M	G	C	E	Q
				stimulating factor
				2 receptor, beta,
				low-affinity
				(granulocyte-
				macrophage)
G2381u6	WIAF-12946	M59941	2458	CSF2RB, colony	CCCCACAGCC[C/A]GAGGGCCTCC	S	C	A	P	P
				stimulating factor
				2 receptor, beta,
				low-affinity
				(granulocyte-
				macrophage)
G2384u1	WIAF-12908	M61831	1000	AHCY, S-adenosyl-	GCCGTGGAGA[A/C]GGTGAACATC	M	A	C	K	T
				homocysteine
				hydrolase
G2387u1	WIAF-12910	M63967	2585	ALDH5, aldehyde	CTGCTGAACC[T/G]CCTGGCAGAC	M	T	G	L	R
				dehydrogenase 5
G2387u2	WIAF-12911	M63967	2996	ALDH5, aldehyde	TATGGCCCAA[C/G]AGCAGGTGCG	M	C	G	T	R
				dehydrogenase 5
G2387u3	WIAF-12954	M63967	2522	ALDH5, aldehyde	GCCCGGGAAG[C/T]CTTCCGCCTG	M	C	T	A	V
				dehydrogenase 5
G2387u4	WIAF-12955	M63967	2448	ALDH5, aldehyde	ACCCTACCAC[C/T]GGGGAGGTCA	S	C	T	T	T
				dehydrogenase 5
G2387u5	WIAF-12956	M63967	2460	ALDH5, aldehyde	GGGAGGTCAT[C/T]GGGCACGTGG	S	C	T	I	I
				dehydrogenase 5
G2387u6	WIAF-12957	M63967	2991	ALDH5, aldehyde	CGGGGTATGG[C/T]CCAACAGCAG	S	C	T	G	G
				dehydrogenase 5
G2387u7	WIAF-12958	M63967	3022	ALDH5, aldehyde	CGCCCAGCAC[A/G]TGGATGTTGA	M	A	G	M	V
				dehydrogenase 5
G2387u8	WIAF-12959	M63967	2943	ALDH5, aldehyde	CCCTCATCAA[G/C]GAGGCAGGCT	M	G	C	K	N
				dehydrogenase 5
G2388u1	WIAF-12888	M64590	588	GLDC, glycine	TGCCACAGAC[G/A]ATTTTGCCGA	S	C	A	T	T
				dehydrogenase
				(decarboxylating;
				glycine decarboxyl-
				ase, glycine cleav-
				age system protein
				P)
G2388u2	WIAF-12889	M64590	651	GLDC, glycine	ACCAGCCTGA[G/A]GTGTCTCAGG	S	G	A	E	E
				dehydrogenase
				(decarboxylating;
				glycine decarboxyl-
				ase, glycine cleav-
				age system protein
				P)
G2388u3	WIAF-12890	M64590	698	GLDC, glycine	CAGACCATGG[T/C]GTGTGACATC	M	T	C	V	A
				dehydrogenase
				(decarboxylating;
				glycine decarboxyl-
				ase, glycine cleav-
				age system protein
				P)
G2388u4	WIAF-12891	M64590	557	GLDC, glycine	TATATTGGCA[T/C]GGGCTATTAT	M	T	C	M	T
				dehydrogenase
				(decarboxylating;
				glycine decarboxyl-
				ase, glycine cleav-
				age system protein
				P)
G2388u5	WIAF-12938	M64590	587	GLDC, glycine	GTGCCACAGA[C/G]GATTTTGCGG	M	C	G	T	R
				dehydrogenase
				(decarboxylating;
				glycine decarboxyl-
				ase, glycine cleav-
				age system protein
				P)
G2388u6	WIAF-12939	M64590	518	GLDC, glycine	CTGCATGCCA[T/C]TTCAAGCAAA	M	T	C	I	T
				dehydrogenase
				(decarboxylating;
				glycine decarboxyl-
				ase, glycine cleav-
				age system protein
				P)
G2388u7	WIAF-12940	M64590	810	GLDC, glycine	GGAAATTTCT[C/T]GTTGATCCCC	S	C	T	L	L
				dehydrogenase
				(decarboxylating;
				glycine decarboxyl-
				ase, glycine cleav-
				age system protein
				P)
G2388u8	WIAF-12941	M64590	1481	GLDC, glycine	CATTGTGGCT[G/A]CTCAGTGAAG	M	G	A	C	Y
				dehydrogenase
				(decarboxylating;
				glycine decarboxyl-
				ase, glycine cleav-
				age system protein
				P)
G2388u9	WIAF-12947	M64590	1841	GLDC, glycine	AAACTGAACA[C/A]TTCGTCTGAA	M	G	A	S	N
				dehydrogenase
				(decarboxylating;
				glycine decarboxyl-
				ase, glycine cleav
				age system protein
				P)
G2388u10	WIAF-12948	M64590	2325	GLDC, glycine	GACAGGTCTA[C/T]CTACACCGGG	S	C	T	Y	Y
				dehydrogenase
				(decarboxylating;
				glycine decarboxyl-
				ase, glycine cleav-
				age system protein
				P)
G2388u11	WIAF-12949	M64590	2362	GLDC, glycine	GGTGGGAATC[T/A]GTCCCCCTGG	M	T	A	C	S
				dehydrogenase
				(decarboxylating;
				glycine decarboxyl-
				ase, glycine cleav-
				age system protein
				P)
G2388u12	WIAF-12950	M64590	3220	GLDC, glycine	TTAGTCCTCT[C/G]TCCCTAAGTT	-	C	G	-	-
				dehydrogenase
				(decarboxylating;
				glycine decarboxyl-
				ase, glycine cleav-
				age system protein
				P)
G2391u1	WIAF-12998	M69238	623	ARNT, aryl hydro-	TGGTGTATGT[G/C]TCTGACTCCG	S	G	C	V	V
				carbon receptor
				nuclear
				translocator
G2391u2	WIAF-13002	M69238	1072	ARNT, aryl hydro-	TGCCTAGTGG[C/T]CATTGGCAGA	M	C	T	A	V
				carbon receptor
				nuclear
				translocator
G2391u3	WIAF-13021	M69238	966	ARNT, aryl hydro-	ACCTCACTTC[G/A]TGGTGGTCCA	M	G	A	V	M
				carbon receptor
				nuclear
				translocator
G2394u1	WIAF-13003	M73747	2061	TSHR, thyroid	TTGCTCGTAC[T/A]CTTCTATCCA	M	T	A	L	H
				stimulating hormone
				receptor
G2394u2	WIAF-13004	M73747	2248	TSHR, thyroid	TTACCCACGA[C/G]ATGAGGCAGG	M	C	G	D	E
				stimulating hormone
				receptor
G2396u1	WIAF-12995	M74542	1027	ALDH3, aldehyde	CCCCCAGTCC[C/G]CGGTGATGCA	M	C	G	P	A
				dehydrogenase 3
G2396u2	WIAF-13019	M74542	1295	ALDH3, aldehyde	GGCAACAACA[G/A]CTTCGAGACT	M	G	A	S	N
				dehydrogenase 3
G2403u1	WIAF-13583	M83670	280	CA4, carbonic	TACGATAAGA[A/T]GCAAACGTGG	M	A	T	K	M
				anhydrase IV
G2409u1	WIAF-10010	HT2156	1268	AGTR1, angiotensin	CCACTCAAAC[C/T9 TTTCAACAAA	M	C	T	L	F
				receptor 1
G2411u1	WIAF-13541	M97759	210	ADORA2B, adenosine	TGGCGGGCAA[C/T]GTGCTGGTGT	S	C	T	N	N
				A2b receptor
G2422u1	WIAF-14077	S90469	375	POR, P450	GCAGCCTGCC[A/G]GAGATCGACA	S	A	G	P	P
				(cytochrome)
				oxidoreductase
G2422u2	WIAF-14078	S90469	852	POR, P450	TCCTGGCTGC[A/G]GTCACCACCA	S	A	G	A	A
				(cytochrome)
				oxidoreductase
G2422u3	WIAF-14082	S90469	1496	POR, P450	AAGGAGCCTG[T/C]CGCCGAGAAC	M	T	C	V	A
				(cytochrome)
				oxidoreductase
G2422u4	WIAF-14099	S90469	1443	POR, P450	AGACCAAGGC[C/T]GGCCGCATCA	S	C	T	A	A
				(cytochrome)
				oxidoreductase
G2422u5	WIAF-14100	S90469	1704	POR, P450	GCCGCCGCTC[G/A]GATGAGGACT	S	G	A	S	S
				(cytochrome)
				oxidoreductase
G2427u1	WIAF-14079	U07919	1369	ALDH6, aldehyde	ACTATGGACT[C/T]ACAGCAGCCG	S	C	T	L	L
				dehydrogenase 6
G2427u2	WIAF-14096	U07919	1347	ALDH6, aldehyde	ATAAAAAGAG[C/T]GAATACCACC	M	C	T	A	V
				dehydrogenase 6
G243u1	WIAF-11684	X57522	926	TAP1, transporter	ATAGCCAGTG[C/G]AGTGCTGGAG	M	C	G	A	G
				1, ABC (ATP
				binding cassette)
G243u2	WIAF-11685	X57522	627	TAP1, transporter	ACCCTACCGC[C/T]TTCGTTGTCA	S	C	T	A	A
				1, ABC (ATP
				binding cassette)
G243u3	WIAF-11686	X57522	538	TAP1, transporter	CCTGCCGGGA[C/G]TTCCCTTGTT	M	C	G	L	V
				1, ABC (ATP
				binding cassette)
G243u4	WIAF-11687	X57522	798	TAP1, transporter	TGGTGGTCCT[C/G]TCCTCTCTTG	S	C	G	L	L
				1, ABC (ATP
				binding cassette)
G243u5	WIAF-11689	X57522	1465	TAP1, transporter	TAGTATTTCA[G/T]GTATCCTGCT	M	G	T	G	C
				1, ABC (ATP
				binding cassette)
G243u6	WIAF-11690	X57522	177	TAP1, transporter	AGAGTCCCAG[A/G]CCCGGCCGGG	S	A	G	R	R
				1, ABC (ATP
				binding cassette)
G243u7	WIAF-11693	X57522	1067	TAP1, transporter	AACATCATGT[C/T]TCGGGTAACA	M	C	T	S	F
				1, ABC (ATP
				binding cassette)
G243u8	WIAF-11665	X57522	1207	TAP1, transporter	GGTCACCCTG[A/G]TCACCCTGCC	M	A	G	I	V
				1, ABC (ATP
				binding cassette)
G243u9	WIAF-11664	X57522	1757	TAP1, transporter	CCAAACCCCC[C/T]ACATGTCTTA	N	C	T	P	L
				1, ABC (ATP
				binding cassette)
G244u1	WIAF-10174	X60592	239	TNFRSF5, tumor	CTTGCGGTCA[A/C]AGCGAATTCC	S	A	G	E	E
				necrosis factor
				receptor super-
				family, member 5
G2441u1	WIAF-13682	U30246	1355	SLC12A2, solute	TGCTTAAGGA[A/G]CATTCCATAC	S	A	G	E	E
				carrier family 12
				(sodium/potassium/
				chloride trans-
				porters), member 2
G2441u2	WIAF-13714	U30246	2691	SLC12A2, solute	AGCCAAATAT[C/G]AGCCATGGCT	M	C	G	Q	E
				carrier family 12
				(sodium/potassium/
				chloride trans-
				porters), member 2
G2443u1	WIAF-14004	U37143	1456	CYP2J2, cytochrome	CTGAAGTTTA[G/A]AATGGGTATC	M	G	A	R	K
				P450, subfamily IIJ
				(arachidonic acid
				epoxygenase)
				polypeptide 2
G2443u2	WIAF-14032	U37143	376	CYP2J2, cytochrome	TTTAAGAAAA[A/G]TGGATTGATT	M	A	G	N	S
				P450, subfamily IIJ
				(arachidonic acid
				epoxygenase)
				polypeptide 2
G2443u3	WIAF-14033	U37143	1502	CYP2J2, cytochrone	TCTGCGCTGT[T/A]CCTCAGGTGT	S	T	A	V	V
				P450, subfamily IIJ
				(arachidonic acid
				epoxygenase)
				polypeptide 2
G2444u1	WIAF-14065	U37519	771	ALDH3, aldehyde	CCCGCACGGA[A/G]TTGCCTCGTG	M	A	G	N	S
				dehydrogenase 3
G2444u2	WIAF-14066	U37519	1698	ALDH3, aldehyde	AAGGAGATCC[G/A]CTACCCACCC	M	G	A	R	H
				dehydrogenase 3
G2445u1	WIAF-14114	U38178	236	CNP, 2′,3′-cyclic	TGCCGGGCGC[C/A]CCTCTCGCTG	M	G	A	R	H
				nucleotide 3′
				phosphodiesterase
G2445u2	WIAF-14115	U38175	849	CNP, 2′,3′-cyclic	GTGCCGCCGA[A/G]GAAAAAGTGC	S	A	G	G	E
				nucleotide 3′
				phosphodiesterase
G2445u3	WIAF-14122	U38178	1655	CNP, 2′,3′-cyclic	GTTATCTTGC[A/T]GAGATCTCTG	M	A	T	Q	L
				nucleotide 3′
				phosphodiesterase
G2445u4	WIAF-14241	X95520	941	CNP, 2′,3′-cyclic	TGCAAAATAT[T/C]CAGGAGACCG	?	T	C	?	?
				nucleotide 3′
				phosphodiesterase
G2445u5	WIAF-14242	X95520	1057	CNP, 2′,3′-cyclic	TCGAGTTGAT[C/T]TTTCAGTGCT	?	C	T	?	?
				nucleotide 3′
				phosphodiesterase
G2445u6	WIAF-14243	X95520	1583	CNP, 2′,3′-cyclic	TCTACTGGCT[C/G]TCTAACTAAT	?	C	G	?	?
				nucleotide 3′
				phosphodiesterase
G2448u1	WIAF-13973	U46689	1895	ALDH10, aldehyde	TTGTCAAGGC[A/T]GAATATTACT	S	A	T	A	A
				dehydrogenase 10
				(fatty aldehyde
				dehydrogenase)
G2457u1	WIAF-13898	U90277	1304	GRIN2A, glutamate	GGTCCCGATG[C/T]ACACCTTGCA	M	C	T	H	Y
				receptor, iono-
				tropic, N-methyl
				D-aspartate 2A
G2457u2	WIAF-13899	U90277	1934	GRIN2A, glutamate	AAGAAGTAAT[G/T]GCACCGTCTC	M	G	T	G	C
				receptor, iono-
				tropic, N-methyl
				D-aspartate 2A
G2457u3	WIAF-13900	U90277	2230	GRIN2A, glutamate	TCGCTGTCAT[A/G]TTCCTGGCTA	M	A	G	I	M
				receptor, iono-
				tropic, N-methyl
				D-aspartate 2A
G2457u4	WIAF-13902	U90277	2916	GRIN2A, glutamate	GGCATCTACA[G/A]CTGCATTCAT	M	G	A	S	N
				receptor, iono-
				tropic, N-methyl
				D-aspartate 2A
G2457u5	WIAF-13903	U90277	3251	GRIN2A, glutamate	CTATGTATTC[C/T]AGGCACAACA	N	C	T	Q	*
				receptor, iono-
				tropic, N-methyl
				D-aspartate 2A
G2457u6	WIAF-13917	U90277	2756	GRIN2A, glutamate	GGACATTGAC[A/C]ACATCCCGGG	M	A	G	N	D
				receptor, iono-
				tropiC, N-methyl
				D-aspartate 2A
G2468u1	WIAF-13642	X04011	1017	CYBB, cytochrome	AGGTGTCCAA[G/A]CTGGAGTGGC	S	G	A	K	K
				b-245, beta poly-
				peptide (chronic
				granulomatous
				disease)
G2473u1	WIAF-13670	X06990	1417	ICAM1, inter-	GGTCACCCGC[G/A]AGGTGACCGT	M	G	A	E	K
				cellular adhesion
				molecule 1 (CD54),
				human rhinovirus
				receptor
G2473u2	WIAF-13695	X06990	179	ICAM1, inter-	GACCAGCCCA[A/T]GTTGTTGGGC	M	A	T	K	M
				cellular adhesion
				molecule 1 (CD54),
				human rhinovirus
				receptor
G2480u1	WIAF-14148	X55330	800	AGA, aspartylgluco-	TTGGCATGGT[T/G]GTAATCCATA	S	T	G	V	V
				saminidase
G2480u2	WIAF-14149	X55330	852	AGA, aspartylgluco-	AAATGGTATA[A/T]AATTCAAAAT	M	A	T	K	*
				saminidase
G2480u3	WIAF-14158	X55330	616	AGA, aspartylgluco-	TTATCTACCA[G/C]TGCTTCTCAA	M	G	C	S	T
				saminidase
G2485u1	WIAF-13612	X59543	2301	RRM1, ribo-	ATTGATCAAA[C/A]CCAATCTTTG	M	G	A	S	N
				nucleotide
				reductase M1
				polypeptide
G2485u2	WIAF-43613	X59543	2410	RRM1, ribo-	ATTTAAGGAC[G/A]AGACCAGCAG	S	G	A	T	T
				nucleotide
				reductase M1
				polypeptide
G2485u3	WIAF-13651	X59543	548	RRM1, ribo-	CAAGTCAACA[T/C]TGGATATTGT	S	T	C	L	L
				nucleotide
				reductase M1
				polypeptide
G2485u4	WIAF-13652	X59543	199	RRM1, ribo-	TGCATGTGAT[C/T]AAGCGAGATG	S	C	T	I	I
				nucleotide
				reductase M1
				polypeptide
G2485u5	WIAF-13653	X59543	1037	RRM1, ribo-	CAACACAGCT[C/A]GATATGTGGA	S	C	A	R	R
				nucleotide
				reductase M1
				polypeptide
G2485u6	WIAF-13660	X59543	1955	RRM1, ribo-	GAAGATTGCA[A/C]ADTATGGTAT	M	A	C	K	Q
				nucleotide
				reductase M1
				polypeptide
G2485u7	WIAF-13877	X59543	860	RRM1, ribo-	GAGTATGAAA[G/C]ATGACAGCAT	M	G	C	E	Q
				nucleotide
				reductase M1
				polypeptide
G2486u1	WIAF-14075	X59618	543	RRM2, ribo-	TCAGCACTGG[G/C]AATCCCTGAA	M	G	C	E	Q
				nucleotide
				reductase M2
				polypeptide
G2486u2	WIAF-14076	X59618	189	RRM2, ribo-	TCGCTGCGCC[T/G]CCACTATGCT	-	T	G	-	-
				nucleotide
				reductase M2
				polypeptide
G2486u3	WIAF-14092	X59618	524	RRM2, ribo-	TTGACCTCTC[C/G]AACGACATTC	S	C	G	S	S
				nucleotide
				reductase M2
				polypeptide
G2488u1	WIAF-13585	X63563	1633	POLR2B, polymerase	CCTTGATGGC[C/A]TATATTTCAG	S	G	A	A	A
				(RNA) II (DNA
				directed) poly-
				peptide B (140 kD)
G2488u2	WIAF-13586	X63563	2452	POLR2B, polymerase	CTGTAGACCG[C/T]GGCTTCTTCA	S	C	T	R	R
				(RNA) II (DNA
				directed) poly-
				peptide B (140 kD)
G2488u3	WIAF-13587	X63563	2740	POLR2B, polymerase	TCAGAACTAG[T/C]GAGACCGGCA	S	T	C	S	S
				(RNA) II (DNA
				directed) poly-
				peptide B (140 kD)
G2488u4	WIAF-13602	X63563	1411	POLR2B, polymerase	GGGGTGATCA[A/G]AAGAAAGCTC	S	A	G	Q	Q
				(RNA) II (DNA
				directed) poly-
				peptide B (140 kD)
G2488u5	WIAF-13603	X63563	2386	POLR2B, polymerase	CAATTGTGGC[C/T]ATTGCATCAT	S	C	T	A	A
				(RNA) II (DNA
				directed) poly-
				peptide B (140 kD)
G2489u1	WIAF-14181	X63564	1346	POLR2A, polymerase	TGGTGGACAA[T/C]GAGCTGCCTG	S	T	C	N	N
				(RNA) II (DNA
				directed) poly-
				peptide A (220 kD)
G2489u2	WIAF-14236	X63564	1647	POLR2A, polymerase	TGAATCTTAG[C/T]GTGACAACTC	?	C	T	?	?
				(RNA) II (DNA
				directed) poly-
				peptide A (220 kD)
G2489u3	WIAF-14237	X63564	2678	POLR2A, polymerase	CTGAATACAA[C/T]AACTTCAAGT	?	C	T	?	?
				(RNA) II (DNA
				directed) poly-
				peptide A (220 kD)
G2489u4	WIAF-14238	X63564	3059	POLR2A, polymerase	AGCTGCGCTA[C/T]GGCGAACACG	?	C	T	?	?
				(RNA) II (DNA
				directed) poly-
				peptide A (220 kD)
G2489u5	WIAF-14239	X63564	3827	POLR2A, polymerase	TGGGCCAGTC[C/T]GCTCGAGATG	?	C	T	?	?
				(RNA) II (DNA
				directed) poly-
				peptide A (220 kD)
G2489u6	WIAF-14240	X63564	3992	POLR2A, polymerase	TGCCTGACTT[T/C]GATGTGGCCC	?	T	C	?	?
				(RNA) II (DNA
				directed) poly-
				peptide A (220 kD)
G2489u7	WIAF-14245	X63564	3938	POLR2A, polymerase	CCCAGAGCAC[G/A]GTGGTGGCAG	?	G	A	?	?
				(RNA) II (DNA
				directed) poly-
				peptide A (220 kD)
G250u1	WIAF-11696	HT0155	1113	IL3RA, interleukin	CTGTGTCTTC[G/C]TGATCTGCAG	M	G	C	V	L
				3 receptor, alpha
				(low affinity)
G251u1	WIAF-11666	HT0240	179	interleukin 1	TGGATAAGAC[C/T]CGAGCTTTGA	S	C	T	T	T
				beta convertase
G251u2	WIAF-11694	HT0240	973	interleukin 1	GATGCTATTA[A/G]GAAAGCCCAC	M	A	G	K	R
				beta convertase
G251u3	WIAF-11695	HT0240	783	interleukin 1	CCCAGATATA[C/T]TACAACTCAA	S	C	T	L	L
				beta convertase
G2513u1	WIAF-13736	HT27365	1721	PLCB3, phospho-	AACTATCTAT[G/A]AAAAGCCAAA	M	G	A	M	I
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u2	WIAF-13737	HT27365	1741	PLCB3, phospho-	AACTATTGGG[A/T]AATCTGTTCA	M	A	T	E	V
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u3	WIAF-13738	HT27365	1697	PLCB3, phospho-	AATCTGTTCA[A/G]TACACGGATT	S	A	G	Q	Q
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u4	WIAF-13739	HT27365	1908	PLCB3, phospho-	CTGTCAGATT[C/A]TAGCAATGAA	M	G	A	V	I
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u5	WIAF-13740	HT27365	2172	PLCB3, phospho-	TATACAGATA[C/T]ACGGAATTCC	M	C	T	H	Y
				lipase C, beta 3
				(phosphotidylino-
				sitol-specific)
G2513u6	WIAF-13744	HT27365	3019	PLCB3, phospho-	TTGAAGGGCC[A/C]AGGAGATCTG	M	A	G	Q	R
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u7	WIAF-13745	HT27365	3024	PLCB3, phospho-	GGGCCAAGCA[G/A]ATCTGTTGAA	M	G	A	D	N
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u8	WIAF-13771	HT27365	1079	PLCB3, phospho-	ACATTTTTGA[T/C]CCTGAGCAAA	S	T	C	D	D
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u9	WIAF-13772	HT27365	1546	PLCB3, phospho-	AAGTTGCCTT[C/T]TGATCCAGAT	M	C	T	S	F
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u10	WIAF-13773	HT27365	1514	PLCB3, phospho-	AATTAAAAAG[A/T]ATGATCATTG	M	A	T	R	S
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u11	WIAF-13774	HT27365	1445	PLCB3, phospho-	AGGTCTTTGG[C/T]AATAAACTCT	S	C	T	G	G
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u12	WIAF-13778	HT27365	2087	PLCB3, phospho-	TTCATATCAA[G/A]ATCATCAGTG	S	G	A	K	K
				lipase C, beta 3
				(phosphotidylino-
				sitol-specific)
G2513u13	WIAF-13779	HT27365	2367	PLCB3, phospho-	TGAATGTTTG[C/T]ACCCTGGATA	N	C	T	Q	*
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u14	WIAF-13782	HT27365	2719	PLCB3, phospho-	CTCATCACCA[G/A]TGACAATACT	M	G	A	S	N
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u15	WIAF-13783	HT27365	2567	PLCB3, phospho-	TTGATGACAT[C/T]TTTAAAATAG	S	C	T	I	I
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u16	WIAF-13784	HT27365	2864	PLCB3, phospho-	TAGAAATGGC[G/A]GACACACTCC	S	G	A	A	A
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u17	WIAF-13785	HT27365	2571	PLCB3, phospho-	TGACATCTTT[A/T]AAATAGCGGT	N	A	T	K	*
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G2513u18	WIAF-13786	HT27365	2706	PLCB3, phospho-	TCTGTCATCT[C/T]GCCTCATCAC	M	C	T	R	W
				lipase C, beta 3
				(phosphatidylino-
				sitol-specific)
G252u1	WIAF-10195	HT0425	397	FCER2, Fc fragment	GAGGGCTGCC[C/T]GGAACGTCTC	M	C	T	R	W
				of IgE, low
				affinity II,
				receptor for
				(CD23A)
G252u2	WIAF-10206	HT0425	930	FCER2, Fc fragment	ATGGGAGCCA[T/C]GTGGACTACA	S	T	C	H	H
				of IgE, low
				affinity II,
				receptor for
				(CD23A)
G253u1	WIAF-10175	HT0573	228	IFNB1, interferon,	GGCTTGAATA[C/T]TGCCTCAACG	S	C	T	Y	Y
				beta 1, fibroblast
G254u1	WIAF-10196	HT0611	466	IL4R, interleukin	TCAGTGCGGA[T/C]AACTATACAC	S	T	C	D	D
				4 receptor
G254u2	WIAF-10198	HT0611	1474	IL4R, interleukin	CATGCCTTCT[T/C]CCACCTTCGG	S	T	C	L	L
				4 receptor
G254u3	WIAF-10207	HT0611	1902	IL4R, interleukin	AGTGGCTATC[A/G]GGAGTTTGTA	M	A	G	Q	R
				4 receptor
G260u1	WIAF-10186	HT1090	453	IL4R, interleukin	TGTTATAATC[C/G]ACAACCCATA	M	C	G	A	G
				1 receptor, type I
G261u1	WIAF-10187	HT1101	434	IL7R, interleukin	CCTCACTGTC[A/G]TCTATCCCCA	M	A	G	I	V
				7 receptor
G261u2	WIAF-10203	HT1101	517	IL7R, interleukin	TTTTAATCCA[T/C]CATCTAGCTT	S	T	C	H	H
				7 receptor
G267u1	WIAF-11735	HT1877	881	IL2RB, interleukin	TCCTCGTGGG[C/T]CTCAGCGGGG	S	C	T	G	G
				2 receptor, beta
G267u2	WIAF-11759	HT1877	379	IL2RB, interleukin	AGTCAAGCAT[C/T]CTGCGCCTGC	M	G	T	S	F
				2 receptor, beta
G268u1	WIAF-11758	HT1985	568	CD19 antigen	GCCTCCGTGT[G/C]TCCCACCGAG	M	G	C	V	L
G268u2	WIAF-11734	HT1985	783	CD19 antigen	ACGATCGCCC[G/T]GCCAGAGATA	S	G	T	P	P
G270u1	WIAF-11736	HT2415	530	IL6R, interleukin	AGGAGGTGGC[A/G]AGAGCCGTGC	S	A	G	A	A
				6 receptor
G270u2	WIAF-11760	HT2415	1590	IL6R, interleukin	CATTGCCATT[G/A]TTCTGAGGTT	M	G	A	V	I
				6 receptor
G270u3	WIAF-11737	HT2415	1510	IL6R, interleukin	CCAGTGCAAG[A/C]TTCTTCTTCA	M	A	C	D	A
				6 receptor
G270u4	WIAF-11761	HT2415	1451	IL6R, interleukin	CTACTAATAA[A/T]GACGATGATA	M	A	T	K	N
				6 receptor
G270u5	WIAF-11766	HT2415	1843	IL6R, interleukin	TTCCCCAGAT[A/C]CCTGGCTGGG	N	A	G	*	W
				6 receptor
G270u6	WIAF-11767	HT2415	1829	IL6R, interleukin	ATACAGACTA[C/T]TTCTTCCCCA	S	C	T	Y	Y
				6 receptor
G271u1	WIAF-11762	HT2531	577	CD2, CD2 antigen	TCAGAGGCTC[A/G]TCACACACAA	M	A	G	I	V
				(p50), sheep red
				blood cell receptor
G271u2	WIAF-11739	HT2531	861	CD2, CD2 antigen	GGAAGCCCCA[A/C]CAAATTCCAG	M	A	C	X	H
				(p50), sheep red
				blood cell receptor
G271u3	WIAF-11768	HT2531	818	CD2, CD2 antigen	CTGGAGACAA[G/A]AGCCCACAGA	M	G	A	R	K
				(p50), sheep red
				blood cell receptor
G271u4	WIAF-11738	HT2531	736	CD2, CD2 antigen	CCTCTTGATG[G/A]TCTTTGTGGC	M	G	A	V	I
				(p50), sheep red
				blood cell receptor
G273u1	WIAF-11763	HT3139	667	IL2RA, interleukin	ATCATCGTGC[C/T]TGGCTGCCAG	M	C	T	P	L
				2 receptor, alpha
G273u2	WIAF-11764	HT3139	956	IL2RA, interleukin	AAACTCCAAT[G/C]CACCCACTGC	M	G	C	M	I
				2 receptor, alpha
G273u3	WIAF-11765	HT3139	701	IL2RA, interleukin	ACGATGACCC[G/A]CCAGAGATCC	S	G	A	P	P
				2 receptor, alpha
G273u4	WIAF-11740	HT3139	1133	IL2RA, interleukin	AAATGACCCA[C/T]GGGAAGACAA	S	C	T	H	H
				2 receptor, alpha
G273u5	WIAF-11769	HT3139	1163	IL2RA, interleukin	AGCCCCAGCT[C/A]ATATGCACAG	S	C	A	L	L
				2 receptor, alpha
G276u1	WIAF-10192	HT3670	644	CD4 antigen	CTCCTAGTAG[C/G]CCCTCAGTGC	M	C	G	S	R
G276u2	WIAF-10193	HT3670	1535	CD4 antigen	CCTGCCAGTG[T/C]CCTCACCGCT	S	T	C	C	C
G276u3	WIAF-10205	HT3670	1217	CD4 antigen	TGATCCTGAC[T/C]TTCAAACTCG	S	T	C	S	S
G277u1	WIAF-10007	D10232	851	RENBP, renin-	CACGTGATTG[A/G]CAAGTTCCTA	M	A	G	D	G
				binding protein
G277u2	WIAF-10032	D10232	842	RENBP, renin-	CTTCGAGCCC[A/G]CGTGATTGAC	M	A	G	H	R
				binding protein
G277u3	WIAF-10042	D10232	634	RENBP, renin-	CCTGGCGGCC[A/G]AATACGCAGA	M	A	G	K	E
				binding protein
G279u1	WIAF-10047	K01740	1658	F8C, coagulation	ACTGATGTCC[G/A]TCCTTTGTAT	M	G	A	R	H
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279u2	WIAF-10049	K01740	2328	F8C, coagulation	CCTTACTGAA[G/A]GTTTCTAGTT	S	G	A	K	K
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279u3	WIAF-10050	K01740	4650	F8C, coagulation	CTGTTCTCCC[G/A]AAACCAGACT	S	G	A	P	P
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279u4	WIAF-10050	K01740	6919	F8C, coagulation	CCAGAAGACA[A/C]TGAAAGTCAC	M	A	G	M	V
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279u5	WIAF-10080	K01740	480	F8C, coagulation	TTAAGAACAT[G/A]GCTTCCCATC	M	G	A	M	I
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279u6	WIAF-10082	K01740	2129	F8C, coagulation	TACATTCTAA[G/A]CATTGGAGCA	M	G	A	S	N
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279u7	WIAF-10084	K01740	2533	F8C, coagulation	GTTTGCACAC[A/G]CAACACCTAT	M	A	G	R	G
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279u8	WIAF-10086	K01740	6639	F8C, coagulation	ACCCTCCAAT[T/C]ATTGCTCGAT	S	T	C	I	I
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279u9	WIAF-10087	K01740	5957	F8C, coagulation	GAGAATTATC[G/A]CTTCCATGCA	M	G	A	R	H
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279a10	WIAF-10495	K01740	5829	F8C, coagulation	TGACAGTACA[G/A]GAATTTGCTC	S	G	A	Q	Q
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279a11	WIAF-10496	K01740	5852	F8C, coagulation	TTTTTCACCA[T/G]CTTTCATGAG	M	T	G	I	S
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279a12	WIAF-10502	K01740	2492	F8C, coagulation	ACCACAATTC[C/T]AGAAAATGAC	M	C	T	P	L
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279a13	WIAF-10503	K01740	6906	F8C, coagulation	TGCAAGTGGA[C/T]TTCCAGAAGA	S	C	T	D	D
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279a14	WIAF-13120	K01740	1980	F8C, coagulation	CAGAGAATAT[A/C]CAACGCTTTC	S	A	c	I	I
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G279a15	WIAF-13121	K01740	1982	F8C, coagulation	GAGAATATAC[A/C]ACGCTTTCTC	M	A	c	Q	P
				factor VIIIc,
				procoagulant
				component
				(hemophilia A)
G282u1	WIAF-10067	L25615	976	AVPR1A, arginine	CGCCTTTCTT[C/A]ATCATCCAGA	M	C	A	F	F
				vasopressin
				receptor 1A
G282u2	WIAF-10070	L25615	460	AVPR1A, arginine	TCGGCATGTT[T/C]GCGTCGGCCT	S	T	C	F	F
				vasopressin
				receptor 1A
G282u3	WIAF-10071	L25615	343	AVPR1A, arginine	GCCTGGCCGA[C/T]CTGGCCGTGG	S	C	T	D	D
				vasopression
				receptor 1A
G282u4	WIAF-10072	L25615	68	AVPR1A, arginine	TCTCTCCGCC[G/A]GTCCCGACGC	M	G	A	G	S
				vasopression
				receptor 1A
G282u5	WIAF-10073	L25615	535	AVPR1A, arginine	AGACTCTGCA[A/G]CAGCCCGCGC	S	A	G	Q	Q
				vasopressin
				receptor 1A
G282u6	WIAF-10092	L25615	1075	AVPR1A, arginine	CCTTGAATAG[C/A]TGCTGTAATC	M	C	A	S	R
				vasopressin
				receptor 1A
G282a7	WIAF-10499	L25615	1089	AVPR1A, arginine	TGTAATCCCT[G/A]GATATACATG	N	G	A	W	*
				vasopressin
				receptor 1A
G284u1	WIAF-10182	M16827	1179	ACADM, acyl-	AATATCCTGT[A/G]GAAAAACTAA	S	A	G	V	V
				Coenzyme A
				dehydrogenase,
				C-4 to C-12
				straight chain
G284a2	WIAF-10515	M16827	696	ACADM, acyl-	TTGTGGAACC[A/G]GATACCCCAG	S	A	G	A	A
				Coenzyme A
				dehydrogenase,
				C-4 to C-12
				straight chain
G285u1	WIAF-10108	M28372	258	ZNF9, zinc finger	CTCTTCCAGA[T/C]ATTTGTTATC	S	T	C	D	D
				protein 9 (a
				cellular retroviral
				nucleic acid
				binding protein)
G289u1	WIAF-10041	M63012	172	PON1, paraoxonase 1	CTCTGAAGAC[A/T]TGGAGATACT	M	A	T	M	L
G290u1	WIAF-10085	M63959	354	LRPAP1, low density	CTCATACGCA[A/G]CCTCAATGTC	M	A	G	N	S
				lipoprotein-related
				protein-associated
				protein 1 (alpha-2-
				macroglobulin
				receptor associated
				protein 1)
G290a2	WIAF-13122	M63959	223	LRPAP1, low density	AGCGACTGCA[T/A]CTTCCTCCCG	M	T	A	H	Q
				lipoprotein-related
				protein-associated
				protein 1 (alpha-2-
				macroglobulin
				receptor associated
				protein 1)
G292u1	WIAF-10180	M74096	1002	ACADL, acyl-	AGTGCAACAT[A/C]AATTAGCAGA	M	A	C	K	Q
				Coenzyme A
				dehydrogenase,
				long chain
G293u1	WIAF-10068	M74775	723	LIPA, lipase A,	AAGGACTTAT[T/C]TGGACACAAA	M	T	C	F	S
				lysosomal acid,
				cholesterol
				esterase (Wolman
				disease)
G293a2	WIAF-10497	M74775	107	LIPA, lipase A,	TGAGGGGTCT[G/A]GAGGGAAACT	M	G	A	G	R
				lysosomal acid,
				cholesterol
				esterase (Wolman
				disease)
G293a3	WIAF-10498	M74775	86	LIPA, lipase A,	GGTTCTCTGG[C/A]CCCTGCATTC	M	C	A	P	T
				lysosomal acid,
				cholesterol
				esterase (Wolman
				disease)
G295u1	WIAF-10057	U04270	1282	KCNH2, potassium	AAAGGAGCGA[A/T]CCCACAATGT	M	A	T	T	S
				voltage-gated
				channel, subfamily
				H, member 2
G295u2	WIAF-10062	U04270	1875	KCNH2, potassium	CGCACTGGCT[A/G]GCCTGCATCT	S	A	G	L	L
				voltage-gated
				channel, subfamily
				H, member 2
G295u3	WIAF-10064	U04270	2040	KCNH2, potassium	ACTTCACCTT[C/T]AGCAGCCTCA	S	C	T	F	F
				voltage-gated
				channel, subfamily
				H, member 2
G295u4	WIAF-10088	U04270	1650	KCNH2, potassium	CCGGCCGCAT[C/T]GCCCTCCACT	S	C	T	I	I
				voltage-gated
				channel, subfamily
				H, member 2
G295u5	WIAF-10090	U04270	2139	KCNH2, potassium	CCCTCATGTA[T/C]GCTAGCATCT	S	T	C	Y	Y
				voltage-gated
				channel, subfamily
				H, member 2
G2951u1	WIAF-14147	HT0030	1334	ZNF42, zinc finger	CCCTGCTCTG[A/G]TCACCACCCG	M	A	G	I	V
				protein 42
				(myeloid-specific
				retinoic acid
				responsive)
G2951u2	WIAF-14157	HT0030	1558	ZNF42, zinc finger	ACCAGCTTAC[G/A]CACACCGAGG	S	G	A	T	T
				protein 42
				(myeloid-specific
				retinoic acid
				responsive)
G2959u1	WIAF-13501	HT0134	1014	GRLP1, gluco-	GTGGAGAGAC[T/C]CTGCATAGCT	S	T	C	T	T
				corticoid receptor
				DNA binding factor 1
G2959u2	WIAF-13518	HT0134	1853	GRLF1, gluco-	GAGCCATCTT[A/C]CAGCCTGTTT	M	A	C	Y	S
				corticoid receptor
				DNA binding factor 1
G296a1	WIAF-10514	U12778	961	ACADSB, acyl-	TATTCCATAT[A/G]TTAAAGAAAG	M	A	G	I	V
				Coenzyme A
				dehydrogenase,
				short/branched
				chain
G2968u1	WIAF-12699	HT0244	1754	SMARCA1, SWI/SNF	CAGAACAAAC[C/T]ACTACGTGTA	M	C	T	P	L
				related, matrix
				associated, actin
				dependent regulator
				of chromatin, sub-
				family a, member 1
G2968u2	WIAF-12716	HT0244	2624	SMARCA1, SWI/SNF	TGGGAACGTT[G/T]CAATGAATTA	M	G	T	C	F
				related, matrix
				associated, actinc
				dependent regulator
				of chromatin, sub-
				family a, member 1
G297u1	WIAF-10109	U516660	402	ECH1, enoyl	ACATGGCTTC[G/A]GACATCCTCC	S	G	A	S	S
				Coenzyme Ahydratase
				1, peroxisomal
G297u2	WIAF-10110	U16660	149	ECH1, enoyl	GCACAAGAGG[A/C]GGCTTCCGGA	M	A	C	E	A
				Coenzyme A hydratase
				1, peroxisomal
G2970u1	WIAF-12746	HT0281	682	BR140: bromodomain-	ATGACATGGA[C/T]GAGCAGGACT	S	C	T	D	D
				containing protein,
				140 kD (peregrin)
G2975U1	WIAF-12729	HT0334	1104	B-cell-specific	ACTTTTCCGG[G/A]ACTCCCTACA	S	G	A	C	G
				transcription
				factor
G2975u2	WIAF-12730	HT0334	1185	B-cell-specific	GCTCCCCCTA[C/T]TATTATACCC	S	C	T	Y	Y
				transcription
				factor
G2976a1	WIAF-12129	HT0340	1600	SATB1, special	GTCCTGCCCC[C/A]CTCATCAGCA	S	C	A	P	P
				AT-rich sequence
				binding protein 1
				(binds to nuclear
				matrix/scaf fold-
				associating DNA's)
G2976u2	WIAF-12743	HT0340	2116	SATB1, special AT-	TGGCCTCTCC[A/G]GCACAGTCAG	S	A	G	P	P
				rich sequence
				binding protein 1
				(binds to nuclear
				matrix/scaf fold-
				associating DNA's)
G2978u1	WIAF-12721	HT0346	1140	MSX1, msh (Droso-	CATAGAGGGT[C/T]CCAGGTCCCC	-	C	T	-	-
				phila) homeo box
				homolog 1 (formerly
				homeo box 7)
G298u1	WIAF-10048	U33837	8995	Human glycoprotein	CCGGACAGGA[G/A]GTGCATTCCC	M	G	A	R	K
				receptor gp330
				precursor, mRNA,
				complete cds.
G298u2	WIAF-10051	U33837	13217	Human glycoprotein	ATGCAGCCAT[C/T]GAACTGCCTA	S	C	T	I	I
				receptor gp330
				precursor, mRNA,
				complete cds.
G298u3	WIAF-10077	U33837	6298	Human glycoprotein	AACTCTTTCA[T/C]TGTTGTTTCA	M	T	C	I	T
				receptor gp330
				precursor, mRNA,
				complete cds.
G298u4	WIAF-10078	U33837	6371	Human glycoprotein	CCATGGTCCC[G/A]GTGGCAGGCC	S	G	A	P	P
				receptor gp330
				precursor, mRNA,
				complete cds.
G298u5	WIAF-10079	U33837	6914	Human glycoprotein	ACTCTGAAGT[G/A]ATTCGTTATG	S	G	A	V	V
				receptor gp330
				precursor, mRNA,
				complete cds.
G298u6	WIAF-10081	U33837	8718	Human glycoprotein	GTTCCAATGC[G/A]CATCTGGGCG	M	G	A	A	T
				receptor gp330
				precursor, mRNA,
				complete cds.
G298u7	WIAF-10083	U33837	9088	Human glycoprotein	ACTTGCTCTG[A/G]AAATGAATTC	M	A	G	E	G
				receptor gp330
				precursor, mRNA,
				complete cds.
G298u8	WIAF-10096	U33837	6949	Human glycoprotein	ACTCCTTATC[G/C]CATCACTCTT	M	G	C	G	A
				receptor gp330
				precursor, mRNA,
				complete cds.
G298u9	WIAF-10097	U33837	7149	Human glycoprotein	TTCCTTCCAA[A/C]ACAATCGTGG	M	A	G	N	D
				receptor gp330
				precursor, mRNA,
				complete cds.
G298u10	WIAF-10100	U33837	8590	Human glycoprotein	TACACAAAAT [C/A]TCATAATTCA	M	G	A	C	Y
				receptor gp330
				precursor, mRNA,
				complete cds.
G298u11	WIAF-10101	U33837	12948	Human glycoprotein	CATCTTTCAA[G/C]ACCACTTATA	M	G	C	D	H
				receptor gp330
				precursor, mRNA,
				complete cds.
G2980u1	WIAF-12723	HT0356	437	TLE1, transducin-	TCATGGCCAC[G/A]GACCCCCACT	M	G	A	G	R
				like enhancer of
				split 1, homolog of
				Drosophila E(sp1)
G2980u2	WIAF-12726	HT0356	2044	TLE1, transducin-	AGTGGCTGGC[A/G]GTGGGCATGG	S	A	G	A	A
				like enhancer of
				split 1, homolog of
				Drosophila E(sp1)
G2980u3	WIAF-12747	HT0356	379	TLE1, transducin-	CCATGGCAGA[G/A]TTGAATGCCA	S	G	A	E	E
				like enhancer of
				split 1, homolog of
				Drosophila E(sp1)
G2980u4	WIAF-12748	HT0356	276	TLE1, transducin-	ATCGCCAAGA[G/A]ATTGAATACG	M	G	A	R	K
				like enhancer of
				split 1, homolog of
				Drosophila E(sp1)
G2980u5	WIAF-12749	HT0356	1876	TLE1, transducin-	GCCACACAGA[C/T]GGAGCCAGCT	S	C	T	D	D
				like enhancer of
				split 1, homolog of
				Drosophila E(sp1)
G2980u6	WIAF-12750	HT0356	1759	TLE1, transducin-	CCGCCTGCTA[C/T]GCCCTGGCCA	S	C	T	Y	Y
				like enhancer of
				split 1, homolog of
				Drosophila E(sp1)
G2981u1	WIAF-12720	HT0357	2206	TLE2, transducin-	ACAAATACAT[T/C]GTGACAGSCT	S	T	C	I	I
				like enhancer of
				split 2, homolog of
				Drosophila E(sp1)
G2981u2	WIAF-12737	HT0357	1036	TLE2, transducin-	CGGACAGCGT[C/T]GCCCTCACCA	S	C	T	V	V
				like enhancer of
				split 2, homolog of
				Drosophila E(sp1)
G2981u3	WIAF-12740	HT0357	2181	TLE2, transducin-	CTGAGTTGTG[A/T]CATCTCCAGA	M	A	T	D	V
				like enhancer of
				split 2, homolog of
				Drosophila E(sp1)
G2983u1	WIAF-12833	HT0360	636	TLE3, transducin-	TGTCACCCTC[G/C]GAAAGCCTCC	S	G	C	S	S
				like enhancer of
				split 3, homolog of
				Drosophila E(sp1)
G2983u2	WIAF-12834	HT0360	1944	TLE3, transducin-	TGGACAACAC[G/A]GTGCGCTCCT	S	G	A	T	T
				like enhancer of
				split 3, homolog of
				Drosophila E(sp1)
G2983u3	WIAF-12848	HT0360	1710	TLE3, transducin-	ACCTGGCCTC[C/A]CCCACGCCCC	S	G	A	S	S
				like enhancer of
				split 3, homolog of
				Drosophila E(sp1)
G2985u1	WIAF-12724	HT0421	995	homeotic protein D3	CGCTTCGCCA[G/A]CGCCAACCTC	M	G	A	S	N
G2985u2	WIAF-12725	HT0421	1003	homeotic protein D3	CACCGCCAAC[C/T]TGCAGGCCAC	S	C	T	L	L
G2986u1	WIAF-14124	HT0468	1197	CSDA, cold shock	GCCGTGGATA[C/T]CGGCCTCCCT	S	C	T	Y	Y
				domain protein A
G2987u1	WIAF-12758	HT0474	2068	ZNF7, zinc	AGTGCTTTTA[C/T]GAATATGCGA	S	C	T	Y	Y
				finger protein 7
				(KOX 4, clone
				HF.16)
G2987u2	WIAF-12773	HT0474	985	ZNF7, zinc	GAGAGAAGCC[G/C]TACGAATGTG	S	G	C	P	P
				finger protein 7
				(KOX 4, clone
				HF.16)
G2987u3	WIAF-12775	HT0474	1278	ZNF7, zinc	AGCCAGCAGT[C/T]GCAGCTGGTT	M	C	T	S	L
				finger protein 7
				(KOX 4, clone
				HF.16)
G3005a1	WIAF-12133	HT0735	1441	homeotic protein	GAGGCAGCGG[C/T]CCCGGGCCTG	S	C	T	G	G
				5.1
G3008a1	WIAF-12134	HT0753	1850	ATF4, activating	TAAAAGAGAG[C/A]GCGGATTCCC	S	G	A	R	R
				transcription
				factor 4 (tax-
				responsive enhancer
				element B67)
G3008u2	WIAF-12798	HT0753	946	ATF4, activating	CCCTTCGACC[C/A]GTCGGGTTTG	M	C	A	P	Q
				transcription
				factor 4 (tax-
				responsive enhancer
				element B67)
G3008u3	WIAF-12812	HT0753	1482	ATF4, activating	CACTGCTTAC[G/A]TTGCCATGAT	M	G	A	V	I
				transcription
				factor 4 (tax-
				responsive enhancer
				element B67)
G3008u4	WIAF-12813	HT0753	1847	ATF4, activating	CTCTAAAAGA[G/C]AGGGCGGATT	M	G	C	E	D
				transcription
				factor 4 (tax-
				responsive enhancer
				element B67)
G301u1	WIAF-10127	U71285	3639	MTR, 5-methyltetra-	TGTGGAGACT[C/T]GCAGACATCG	S	C	T	L	L
				hydrofolate-
				homocysteine
				methyltransferase
G3012u1	WIAF-12794	HT0873	402	MAD, MAX	TGGTGCCACT[C/T]GGACCCGAAT	S	G	T	L	L
				dimerization
				protein
G3014u1	WIAF-14183	HT0899	274	homeotic protein 2,	AAAAGACTCA[G/A]TACTTGGCCT	S	G	A	Q	Q
				distal-less
G3020u1	WIAF-12797	HT0956	852	MLLT3, myeloid/	GTGCCTTCAA[A/G]GAACCTTCCA	S	A	G	K	K
				lymphoid or mixed-
				lineage leukemia
				(trithorax
				(Drosophila)
				homolog);
				translocated to, 3
G3023u1	WIAF-13724	HT0966	381	zinc finger, X-	GCTGCAGCAA[G/A]CAATATGACA	S	G	A	K	K
				linked, duplicated
				A
G3023u2	WIAF-13725	HT0966	220	zinc finger, X-	GGCCAAACTC[G/A]GCGCCCACCA	M	G	A	G	S
				linked, duplicated
				A
G3023u3	WIAF-13726	HT0966	69	zinc finger, X-	AGTCGCACGA[T/C]AAACTGCGGC	S	T	C	D	D
				linked, duplicated
				A
G3023u4	WIAF-13727	HT0966	249	zinc finger, X-	ACTTCGAACC[C/T]CACACCCCTT	S	C	T	P	P
				linked, duplicated
				A
G3023u5	WIAF-13765	HT0966	661	zinc finger, X-	CAGGTTCTCT[G/A]CTCGCAGTAG	M	G	A	A	T
				linked, duplicated
				A
G3023u6	WIAF-13766	HT0966	1302	zinc finger, X-	TGACTCCTTC[C/T]AGCACCCTTT	S	G	T	S	S
				linked, duplicated
				A
G3027u1	WIAF-12800	HT1035	124	HOXB7, homeo box B7	TTATGCGAAT[G/A]CTTTATTTTC	M	G	A	A	T
G3027u2	WIAF-12816	HT1035	450	HOXB7, homeo box B7	GCCACTCGCA[C/T]TTCGCGCCCC	S	C	T	D	D
G3028u1	WIAF-12806	HT1037	701	homeotic protein C8	AGACCCTCGA[A/G]CTCCAGAACC	S	A	G	E	E
G3029u1	WIAF-14153	HT1100	441	zinc finger	TCAGACTCAG[G/A]CAAAACTCCG	S	G	A	R	R
				protein 8
G3029u2	WIAF-14155	HT1100	1416	zinc finger	GCCGTCAACA[A/G]TCCTCGACCA	S	A	G	Q	Q
				protein 8
G303u1	WIAF-10000	X13916	4110	LRP1, low density	ATGGAGCTGG[C/A]GCCCGACAAC	M	G	A	G	E
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u2	WIAF-10001	X13916	4012	LRP1, low density	GCGAGCTCTG[C/T]GACCACTGCT	S	C	T	C	C
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u3	WIAF-10002	X13916	4702	LRP1, low density	GCCTGCCCCG[C/T]ATTGAGGCAG	S	C	T	R	R
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u4	WIAF-10003	X13916	6395	LRP1, low density	CTGGATCGCA[G/A]GCAACATCTA	M	G	A	G	S
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u5	WIAF-10004	X13916	6937	LRP1, low density	AAGGCACCAA[C/T]GTGTGCGCGG	S	C	T	N	N
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u6	WIAF-10005	X13916	9391	LRP1, low density	GGCTGAAGGA[T/C]GACGGCCGCA	S	T	C	D	D
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u7	WIAF-10011	X13916	766	LRP1, low density	ACTGCATCGA[C/T]GGCTCAGATG	S	C	T	D	D
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u8	WIAF-10015	X13916	9040	LRP1, low density	ACCCGACCTG[C/T]GGCCCCAGTG	S	C	T	C	C
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u9	WIAF-10019	X13916	11749	LRP1, low density	CCCTGCGCTG[C/T]AACATGTTCG	S	C	T	C	C
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u10	WIAF-10020	X13916	1917	LRP1, low density	GACCAGTATG[G/A]GAAGCCGGGT	M	G	A	G	E
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u11	WIAF-10021	X13916	4810	LRP1, low density	AGAAGCGCAT[C/T]CTTTGGATTG	S	C	T	I	I
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u12	WIAF-10022	X13916	6367	LRP1, low density	TTGGCCGTGT[G/C]GAGGGCATTG	S	G	C	V	V
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u13	WIAF-10023	X13916	6247	LRP1, low density	CTGTCCGCAT[C/T]GACTTCCACG	S	C	T	I	I
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u14	WIAF-10024	X13916	8371	LRP1, low density	ACGCCTCAGA[T/C]GAGATGAACT	S	T	C	D	D
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u15	WIAF-10030	X13916	11395	LRP1, low density	ACGGCAGCGA[C/T]GAGGAGGCCT	S	C	T	D	D
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u16	WIAF-10031	X13916	12763	LRP1, low density	ACGTCTTTGA[G/A]GATTACATCT	S	G	A	E	E
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u17	WIAF-10035	X13916	640	LRP1, low density	ACGGATCTGA[C/T]GAGGCCCCTG	S	C	T	D	D
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u18	WIAF-10037	X13916	1609	LRP1, low density	GCCGCCTTGT[C/T]TACTGGGCAG	S	C	T	V	V
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u19	WIAF-10038	X13916	1629	LRP1, low density	GATGCCTATC[T/G]GGACTATATT	M	T	G	L	R
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u20	WIAF-10039	X13916	2210	LRP1, low density	CACCAGCTAC[C/T]TCATTGGCCG	M	C	T	L	F
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u21	WIAF-10043	X13916	7287	LRP1, low density	GATGGCTCCA[G/A]GAGGATCACC	M	G	A	R	K
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u22	WIAF-10044	X13916	8258	LRP1, low density	CTCTGACGAC[A/G]TCCCTTGCAA	M	A	G	I	V
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G303u23	WIAF-10045	X13916	11871	LRP1, low density	GTGCGCACCG[A/G]GAAAGCCGCC	M	A	G	E	G
				lipoprotein-
				related protein 1
				(alpha-2-macro-
				globulin receptor)
G3031u1	WIAF-14097	HT1128	611	PSMC3, proteasome	TGGGGATCCA[A/C]CCTCCAAAAG	S	A	G	Q	Q
				(prosome, macro-
				pain) 26S subunit,
				ATPase, 3
G3034u2	WIAF-12837	HT1182	421	TCF12, tran-	ATCTTCAATT[A/C]TGGGTTCCTT	M	A	G	M	V
				scription factor 12
				(HTF4, helix-loop-
				helix transcription
				factors 4)
G3038u1	WIAF-12864	HT1373	1700	NFKB1, nuclear	AGAGAAGGCT[A/G]TGCAGCTTGC	M	A	G	M	V
				factor of kappa
				light polypeptide
				gene enhancer in
				B-cells 1 (p105)
G3038u2	WIAF-12881	HT1373	1936	NFKB1, nuclear	TGTACCAGAC[G/A]CCCTTGCACT	S	G	A	T	T
				factor of kappa
				light polypeptide
				gene enhancer in
				B-cells 1 (p105)
G3038u3	WIAF-12882	HT1373	2641	NFKB1, nuclear	AGCTGCACCT[G/C]TATAAGTTAC	S	G	C	L	L
				factor of kappa
				light polypeptide
				gene enhancer in
				B-cells 1 (p105)
G3039u1	WIAF-13027	HT1375	3761	GLI3, GLI-Kruppel	AACAGCCCCG[G/T]AACTCCCACC	M	G	T	G	V
				family member
				GLI3 (Greig
				cephalopoly-
				syndactyly
				syndrome)
G3039u2	WIAF-13028	HT1375	3963	GLI3, CLI-Kruppel	CGCCAAATGA[G/T]TCAGCTGGCA	M	G	T	E	D
				family member
				GLI3 (Greig
				cephalopoly-
				syndactyly
				syndrome)
G304u1	WIAF-12242	HT637	158	FABP3, fatty acid	CTCACCCTAA[A/C]AACACACAGC	M	A	G	K	R
				binding protein
				3, muscle and heart
				(mammary derived
				growth inhibitor)
G3043u1	WIAF-12867	HT1486	842	IRF2, interferon	GTGCCGAGGG[G/A]CGGCCACACT	S	G	A	G	G
				regulatory
				factor 2
G3047u1	WIAF-12875	HT1518	1233	transcription	TCCGTTTCCT[C/T]GAGAGCCTGC	S	C	T	L	L
				factor 1, nucleolar
G3047u2	WIAF-12876	HT1518	1746	transcription	GGATTAAGAA[G/A]GCACCCGAAG	S	G	A	K	K
				factor 1, nucleolar
G3047u3	WIAF-12877	HT1518	1829	transcription	TCCAAGAAGA[T/C]GAAATTCCAG	M	T	C	M	T
				factor 1, nucleolar
G3048u1	WIAF-12884	HT1530	628	transcription	AGTGGAGCGT[C/T]GCCGCCGAGA	M	C	T	R	C
				factor USF
G305u1	WIAF-10150	HT0034	777	prolyl 4-hydroxy-	CCCTTGTCAT[C/T]GAGTTCACCG	S	C	T	I	I
				lase, beta subunit/
				protein disulfide
				isomerase/thyroid
				hormone-binding
				protein, alt.
				transcript 1
G305u21	WIAF-10154	HT0034	186	prolyl 4-hydroxy-	TGGCCGCCCA[C/A]AAGTACCTCC	M	C	A	H	Q
				lase, beta subunit/
				protein disulfide
				isomerase/thyroid
				hormone-binding
				protein, alt.
				transcript 1
G305u3	WIAF-10155	HT0034	1428	prolyl 4-hydroxy-	GGACGGTCAT[T/C]GATTACAACG	S	T	C	I	I
				lase, beta subunit/
				protein disulfide
				isomerase/thyroid
				hormone-binding
				protein, alt,
				transcript 1
G3050u1	WIAF-12860	HT1558	2098	PSRG1: female	AACATTGCAA[T/C]GGCATTTTGA	S	T	C	N	N
				sterile homeotic
				related gene 1
				(mouse homolog)
G3050u2	WIAF-12861	HT1558	2845	FSRG1: female	TAGGCCCTTC[T/C]GGCTTTGGAC	S	T	C	S	S
				sterile homeotic
				related gene 1
				(mouse homolog)
G3050u3	WIAF-12862	HT1558	3409	FSRG1: female	CCTCGTCGTC[G/A]TCTTCAGACA	S	G	A	S	S
				sterile homeotic
				related gene 1
				(mouse homolog)
G3050u4	WIAF-12874	HT1558	1699	FSRG1: female	TCTCTTCTGT[G/C]TCACACACAG	S	G	C	V	V
				sterile homeotic
				related gene 1
				(mouse homolog)
G3050u5	WIAF-12878	HT1558	2093	FSRG1: female	GTTAAAACAT[T/G]GCAATGGCAT	M	T	G	C	G
				sterile homeotic
				related gene 1
				(mouse homolog)
G3050u6	WIAF-12879	HT1558	2746	FSRG1: female	CTGGGGCCGA[C/T]GAAGATGACA	S	C	T	D	D
				sterile homeotic
				related gene 1
				(mouse homolog)
G3051u1	WIAF-12866	HT1569	1423	MEF2B, MADS box	CTTGGCCGAC[G/A]GCTGGCCCCG	S	G	A	T	T
				transcription
				enhancer factor 2,
				polypeptide B
				(myocyte enhancer
				factor 2B)
G3051u2	WIAF-13022	HT1569	661	MEF2B, MADS box	CAGACTACAG[C/T]GAGCCCCACG	S	C	T	S	S
				transcription
				enhancer factor 2,
				polypeptide B
				(myocyte enhancer
				factor 2B)
G3057a1	WIAF-12142	HT1669	5565	alpha-fetoprotein	AGACTGCTCT[T/C]GAGGCTCATA	S	T	C	L	L
				enhancer-binding
				protein
G3057a2	WIAF-12143	HT1669	5634	alpha-fetoprotein	CTCTGTCTGC[C/A]ATGCTCTTAG	S	G	A	A	A
				enhancer-binding
				protein
G3057a3	WIAF-12144	HT1669	5664	alpha-fetoprotein	GGGGACTCCA[G/T]ATGAAAGGAG	M	G	T	Q	H
				enhancer-binding
				protein
G3057a4	WIAF-12145	HT1669	5703	alpha-fetoprotein	GCTTTTCCCA[C/T]CTACCCCCAA	S	C	T	H	H
				enhancer-binding
				protein
G3057u5	WIAF-12885	HT1669	2227	alpha-fetoprotein	TCTGGAGATC[C/T]ATATGAGGTC	M	C	T	H	Y
				enhancer-binding
				protein
G3057u6	WIAF-12892	HT1669	3720	alpha-fetoprotein	AGACCTTGCC[G/A]GCTCAGCTAC	S	G	A	P	P
				enhancer-binding
				protein
G3057u7	WIAF-12893	HT1669	4137	alpha-fetoprotein	CAAGGTTTAC[G/A]GACTACCACC	S	G	A	T	T
				enhancer-binding
				protein
G3057u8	WIAF-12897	HT1669	4783	alpha-fetoprotein	GAAGACCAAC[A/C]CTCCCCAGCA	M	A	C	T	P
				enhancer-binding
				protein
G3057u9	WIAF-12898	HT1669	5215	alpha-fetoprotein	TCCAACCTCC[A/C]CAATGAACAC	M	A	C	T	P
				enhancer-binding
				protein
G3057u10	WIAF-12904	HT1669	7266	alpha-fetoprotein	CCCTGCAGCC[C/TI GCGTTGACTT	S	C	T	A	A
				enhancer-binding
				protein
G3057u11	WIAF-12907	HT1669	8345	alpha-fetoprotein	CCAACACACG[A/C]CTATTCGGAG	M	A	C	D	A
				enhancer-binding
				protein
G3057u12	WIAF-12943	HT1669	4257	alpha-fetoprotein	TGGTGTGGTT[T/C]CAGAATGCCC	S	T	C	F	F
				enhancer-binding
				protein
G057u13	WIAF-12951	HT1669	7333	alpha-fetoprotein	ACCAGGCTTT[T/A]CTCCTTATTA	M	T	A	S	T
				enhancer-binding
				protein
G3057u14	WIAF-13030	HT1669	303	alpha-fetoprotein	GCAHCCTGTC[C/A]GAGGACGAGT	S	G	A	S	S
				enhancer-binding
				protein
G3057u15	WIAF-13031	HT1669	777	alpha-fetoprotein	GCCTTCCAGA[G/A]GACGACGAGG	S	G	A	E	E
				enhancer-binding
				protein
G306u1	WIAF-10118	HT0040	1618	CPT2, carnitine	CTCTACTGCC[C/A]TCCACTTTGA	M	G	A	V	I
				palmitoyl-
				transferase II
G307u1	WIAF-10076	HT0114	110	EDN2, endothelin 2	CGTTGCGCTA[G/A]CCCTGCTCGT	M	G	A	A	T
G3070u1	WIAF-12972	HT2085	625	pre-B-cell leukemia	AGAAATATGA[A/C]CAGGCATGTA	S	A	G	E	E
				transcription
				factor 3
G3070u2	WIAF-12973	HT2085	841	pre-B-cell leukemia	GTAACTTCAG[T/C]AAACAGGCCA	S	T	C	S	S
				transcription
				factor 3
G3071u1	WIAF-12886	HT2086	995	AGER, advanced	CCTGCGAGGC[T/C]GTGATGATCC	S	T	C	A	A
				glycosylation end
				product-specific
				receptor
G3071u2	WIAF-12887	HT2086	1475	AGER, advanced	GAGGCCAGAT[C/G]TACAGCCCAC	M	C	G	I	M
				glycosylation end
				product-specific
				receptor
G3071u3	WIAF-12935	HT2086	933	AGER, advanced	ACGCATGGTG[A/G]GCATCATCCA	M	A	G	S	G
				glycosylation end
				product-specific
				receptor
G3071u4	WIAF-12936	HT2086	1052	AGER, advanced	GTAACTTCAC(C/T]AAACAGGCCA	S	C	T	S	S
				glycosylation end
				product-specific
				receptor
G3071u5	WIAF-12937	HT2086	836	AGER, advanced	AGAAGTATGA[G/A]CAGGCATGTA	S	G	A	E	E
				glycosylation end
				product-specific
				receptor
G308u1	WIAF-10094	HT0192	484	ANX4, annexin IV	ATGGACGGAG[C/G]CTTGAAGATG	M	C	G	S	R
				(placental anti-
				coagulant protein
				II)
G308u2	WIAF-10095	HT0192	333	ANX4, annexin IV	GGGATCATGA[C/T]GCCCACGGTC	M	C	T	T	M
				(placental anti-
				coagulant protein
				II)
G3081u1	WIAF-12997	HT2188	689	PSMC2, proteasome	GGCATTGAGC[C/T]TCCCAAGGGC	M	C	T	P	L
				(prosome, macro-
				pain) 26S subunit,
				ATPase, 2
G3083u1	WIAF-12976	HT2228	106	IGHMBP2, immuno-	TGCTGGAGCT[T/C]GAGAGAGACG	S	T	C	L	L
				globulin mu
				binding protein 2
G3083u2	WIAF-12985	HT2228	2260	IGHMBP2, immuno-	TGGAGTTCAT[G/C]GCCAGCAAGA	M	G	C	M	I
				globulin mu
				binding protein 2
G3083u3	WIAF-12986	HT2228	2060	IGHMBP2, inmuno-	GGGACCTGCT[A/G]CGTCCACCAG	M	A	G	T	A
				globulin mu
				binding protein 2
G3083u4	WIAF-12987	HT2228	2365	IGHMBP2, immuno-	ACGACAGTTC[C/T]GGGGAAGGGA	S	C	T	S	S
				globulin mu
				binding protein 2
G3083u5	WIAF-13005	HT2228	411	IGHMBP2, immuno-	TTTGATGAGT[C/T]CCACGATTTC	M	C	T	S	F
				globulin mu
				binding protein 2
G3083u6	WIAF-13006	HT2228	272	IGHMBP2, immuno-	ATACGGGTCC[G/A]CGGCAGCTCT	M	G	A	A	T
				globulin mu
				binding protein 2
G3083u7	WIAF-13010	HT2228	2581	IGHMBP2, immuno-	TCAGGAGCGC[G/A]CAGGGGCAGC	S	G	A	A	A
				globulin mu
				binding protein 2
G3083u8	WIAF-13011	HT2228	2594	IGHMBP2, immuno-	GGGGCAGCCC[G/A]CCAGCAAGGA	M	G	A	A	T
				globulin mu
				binding protein 2
G3088u1	WIAF-12984	HT2318	884	HIVEP1, human	TGTGGCACTA[C/T]GTCCCCCTCC	M	C	T	T	M
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3088u2	WIAF-12988	HT2318	2469	HIVEP1, human	TCTTGTCACC[A/G]CGTCAACACC	S	A	G	P	P
				immunodeficiency
				virus type I
				enhancer-binding
				protein
G3088u3	WIAF-12989	HT2318	3066	HIVEP1, human	TTCTTGGTAC[T/C]GGACAGTCCC	S	T	C	T	T
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3088u4	WIAF-12991	HT2318	4008	HIVEP1, human	TTATCCGGCA[G/T]CACAACATCC	M	G	T	Q	H
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3088u5	WIAF-12992	HT2318	4880	HIVEP1, human	CAAATCCATG[C/G]ACCGCCTAGC	M	C	G	A	G
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3088u6	WIAF-12993	HT2318	5148	HIVEP1, human	TTGACAGCAT[G/A]TCTAATTCGC	M	G	A	M	I
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3088u7	WIAF-12999	HT2318	5834	HIVEP1, human	CCAGCTGATA[A/C]TTCATCAACA	M	A	G	N	S
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3088u8	WIAF-13000	HT2318	6065	HIVEP1, human	CAAAGTCAAC[G/A]GCCAGTCACT	M	G	A	R	Q
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3088u9	WIAF-13001	HT2318	7652	HIVEP1, human	CATAGGAATA[C/T]GGTCACACAA	M	C	T	T	M
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G30B8u10	WIAF-13008	HT2318	741	HIVEP1, human	TTCTGCAGCA[A/G]CCATCTGAAC	S	A	G	Q	Q
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3088u11	WIAF-13009	HT2318	948	HIVEP1, human	CAGAACTGAG[C/T]ACCTTGTCAC	S	C	T	S	S
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3088u12	WIAF-13012	HT2318	1909	HIVEP1, human	TGAAACTTTA[C/T]TAAAATCAAG	S	C	T	L	L
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3088u13	WIAF-13013	HT2318	2803	HIVEP1, human	TCTTCTGTCT[G/A]TACCTTCACT	M	G	A	V	I
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3088u14	WIAF-13015	HT2318	3342	HIVEP1, human	GCGGTCTGCA[A/G]CCTCAGATTC	S	A	G	Q	Q
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3088u15	WIAF-13016	HT2318	3542	HIVEP1, human	CCTAAACATA[G/A]TGTTACCATA	M	G	A	S	N
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3088u16	WIAF-13017	HT2318	4972	HIVEP1, human	TGGGTCTTCT[A/G]AAAGTGAGGA	M	A	G	K	E
				immunodeficiency
				virus type I
				enhancer-binding
				protein 1
G3095u1	WIAF-12994	HT2435	701	TCF2, transcription	CCGCTCTGTA[C/T]ACCTGGTACG	S	C	T	Y	Y
				factor 2, hepatic;
				LF-B3; variant
				hepatic nuclear
				factor
G3095u2	WIAF-13018	HT2435	362	TCF2, transcription	GGGCCGAGCC[C/T]GACACCAAGC	S	C	T	P	P
				factor 2, hepatic;
				LF-B3; variant
				hepatic nuclear
				factor
G3095u3	WIAF-13020	HT2435	1620	TCF2, transcription	CCAGTTCTCC[C/T]AGCAGCTGCA	N	C	T	Q	*
				factor 2, hepatic;
				LF-B3; variant
				hepatic nuclear
				factor
G3100a1	WIAF-12147	HT2483	526	ZNF141, zinc finger	GAATGAGTGT[A/G]AGTTGCAGAA	M	A	G	K	E
				protein 141 (dione
				pHZ-44)
G3102u1	WIAF-12975	HT2508	259	NRF1, nuclear	CGCCTTCTTC[G/T]CCCGAGGACA	S	G	T	S	S
				respiratory factor
				1
G3103u1	WIAF-13617	HT2511	1106	E2F2, E2F	CCTTGGACCA[G/T]CTCATCCAGA	M	H	T	Q	H
				transcription
				factor 2
C3103u2	WIAF-13659	HT2511	1154	E2F2, E2F	CTGAGGACAA[G/A]GCCAACAAGA	S	G	A	K	K
				transcription
				factor 2
G311u1	WIAF-10291	HT0402	1339	A2M, alpha-2-macro-	GTCCCTGTTA[C/T]GGCTACCAGT	S	C	T	Y	Y
				globulin
G311u2	WIAF-10292	HT0402	1201	A2M, alpha-2-macro-	TCATATTCAT[C/T]AGAGGAAATG	S	C	T	I	I
				globulin
G311u3	WIAF-10293	HT0402	3041	A2M, alpha-2-macro-	TACTCCAGAG[C/A]TCAACTCCAA	M	G	A	V	I
				globulin
G311u4	WIAF-10294	HT0402	3676	A2M, alpha-2-macro-	TGACATCCTA[T/C]GTGCTCCTCC	S	T	C	Y	Y
				globulin
G311u5	WIAF-10296	HT0402	3364	A2M, alpha-2-macro-	ATATCACCAT[C/T]GCCCTTCTGG	S	C	T	I	I
				globulin
G311u6	WIAF-10297	HT0402	3203	A2M, alpha-2-macro-	CCAAGCTCGA[G/T]CCTACATCTT	M	G	T	A	S
				globulin
G311a7	WIAF-10494	HT0402	1122	A2M, alpha-2-macro-	TCACACTTTC[G/A]ACAGGGAATT	M	G	A	R	Q
				globulin
G3119u1	WIAF-13947	HT2654	2876	GLI, glioma-	TTTCTGGGCG[G/A]TTCCCAGGTT	M	G	A	G	D
				associated oncogene
				homolog (zinc
				finger protein)
G3119u2	WIAF-13959	HT2654	654	GLI, glioma-	AGTGCCGGGA[G/A]GAACCCTTGG	S	G	A	E	E
				associated oncogene
				homolog (zinc
				finger protein)
G3119u3	WIAF-13965	HT2654	3376	GLI, glioma-	TGGGGAAACA[G/C]AATTCCTCAA	M	G	C	E	Q
				associated oncogene
				homolog (zinc
				finger protein)
G312u1	WIAF-10006	HT0428	898	PLAU, plasminogen	CTCACCACAA[C/T]CACATTCCCT	S	C	T	N	N
				activator,
				urokinase
G312u2	WIAF-10029	HT0428	498	PLAU, plasminogen	GGCCTAAACC[C/T]GCTTGTCCAA	M	C	T	P	L
				activator,
				urokinase
G312a3	WIAF-10521	HT0428	767	PLAU, plasminogen	TGATTACCCA[A/C]AGAAGGACGA	M	A	C	K	Q
				activator,
				urokinase
G3125u1	WIAF-13675	HT2674	740	GTF2F2, general	ACATCACAAA[A/G]CAACCTGTGG	S	A	G	K	K
				transcription
				factor hF, poly-
				peptide 2 (30 kD
				subunit)
G313u1	WIAF-10129	HT0462	3086	platelet-derived	CATGCGTGTG[C/A]ACTCAGACAA	M	G	A	D	N
				growth factor,
				alpha polypeptide
				(GB:M21574)
G313u2	WIAF-10130	HT0462	1078	platelet-derived	ATGAGAAAGG[T/C]TTCATTGAAA	S	T	G	G	G
				growth factor,
				alpha polypeptide
				(CB:M21574)
G313u3	WIAF-10133	HT0462	1571	platelet-derived	GGAGATCCAC[T/C]CCCCAGACAG	M	T	C	S	P
				growth factor,
				alpha polypeptide
				(CB:M21574)
G313u4	WIAF-10135	HT0462	2611	platelet-derived	CTCGCAACGT[C/T]CTCCTGGCAC	S	C	T	V	V
				growth factor,
				alpha polypeptide
				(CB:M21574)
C314u1	WIAF-10069	HT0467	1890	ALOX15,	TCAGCCAGGA[G/A]CTGGCTGCCC	S	G	A	E	E
				arachidonate 15-
				lipoxygenase
G3141u1	WIAF-13934	HT27498	878	NFATC3, nuclear	CCAGAGGATA[G/A]CTGGCTACTC	M	G	A	S	N
				factor of activated
				T-cells,
				cytoplasmic 3
G3141u2	WIAF-13936	HT27498	1189	NFATC3, nuclear	GCCTGCCTCA[T/C]GCAATGGGAA	M	T	C	C	R
				factor of activated
				T-cells,
				cytoplasmic 3
G3141u3	WIAF-13938	HT27498	2241	NFATC3, nuclear	CTCTGCGGGG[T/C]TTCCCTTCAG	S	T	C	G	G
				factor of activated
				T-cells,
				cytoplasmic 3
C3141u4	WIAF-13944	HT27498	702	NFATC3, nuclear	ATGCCTCTGA[C/T]CACGCAGCCC	S	C	T	D	D
				factor of activated
				T-cells,
				cytoplasmic 3
G3159u1	WIAF-13891	HT2757	523	SP4, Sp4 tran-	CTTCAAAAGA[C/A]AATAACGTTT	S	G	A	E	E
				scription factor
G3159u2	WIAF-13892	HT2757	1514	SP4, Sp4 tran-	ACAGAATGTT[C/T]AACTTCAAGC	N	C	T	Q	*
				scription factor
G3159u3	WIAF-13893	HT2757	2236	SP4, Sp4 tran-	TGTTTTGTGG[C/T]AAAAGATTCA	S	C	T	G	G
				scription factor
G3165u1	WIAF-13860	HT27636	437	transcription	AGCAGCTCAC[A/G]GAGGAACTGA	S	A	G	T	T
				factor B-ATF
G3165u2	WIAF-13861	HT27636	512	transcription	CCACCACGCC[C/G]TCGCCCCCCG	S	C	G	P	P
				factor B-ATF
G3173u1	WIAF-13556	HT2772	1686	ZNF74, zinc finger	TGCACAGCGA[G/A]GGGAAGCCCT	S	G	A	E	E
				protein 74 (Cos52)
G3175u1	WIAF-13948	HT2776	2037	transcriptional	TGTTCGGACC[A/G]GAAGCACCCA	S	A	G	P	P
				regulator, via
				glucocorticoid
				receptor
G3182u1	WIAF-14036	HT2783	1614	MHC2TA, MHC class	ATCCTAGACG[C/G]CTTCGAGGAG	M	C	G	A	G
				II transactivator
G3182u2	WIAF-14037	HT2783	2791	MHC2TA, MHC class	TGAGCGACAC[G/A]GTGGCGCTGT	S	G	A	T	T
				II transactivator
C3182u3	WIAF-14059	HT2783	1657	MHC2TA, MHC class	TGCACAGCAC[C/A]TGCGGACCGG	S	G	A	T	T
				II transactivator
G3182u4	WIAF-14060	HT2783	1606	MHC2TA, MHC class	TTCTGCTCAT[C/T]CTAGACGCCT	S	C	T	I	I
				II transactivator
G3183u1	WIAF-13950	HT27861	392	zinc finger protein	TACTCTAGAG[G/A]AGCCTGTTGG	M	G	A	E	K
				C2H2-150
G3184u1	WIAF-13864	HT27862	271	zinc finger protein	GAAACTCCAG[T/G]TCAAAGACTT	M	T	G	F	V
				C2H2-171
G3184u2	WIAF-13865	HT27862	248	zinc finger protein	CTGCTTGAAT[T/C]CATGTATGAR	M	T	C	F	S
				C2H2-171
G320u1	WIAF-10136	HT0791	552	ANX7, annexin VII	CCAACTTCCA[T/C]GCTATAAGAG	S	T	C	D	D
				(synexin)
G320u2	WIAF-10137	HT0791	1350	ANX7, annexin VII	TTGACCTTGT[A/G]CAAATAAAAC	S	A	G	V	V
				(synexin)
G3208u1	WIAF-14186	HT27930	485	zinc finger	GTCACAAGTC[A/C]GCCCTAATTG	S	A	G	S	S
				protein ZNF37A
G3218u1	WIAF-13526	HT28104	187	zinc finger	CCCGACAGCT[C/T]ATTAAGAAAG	M	C	T	H	Y
				protein ZNF169,
				Krueppel-type
G323u1	WIAF-10066	HT0915	1361	Homo sapiens	ACTTCTGTGA[C/T]GTCCAGCGCT	S	C	T	D	D
				inducible nitric
				oxide synthase
				(NOS) mRNA,
				complete cds.
G325u1	WIAF-10106	HT0962	3817	FBN1, fibrillin 1	TGTGAATGCC[C/T]GCCTGGCCAT	M	C	T	P	L
				(Marfan syndrome)
G325u2	WIAF-10113	HT0962	722	FBN1, fibrillin 1	AGATACCTCC[T/C]TCCTCTGGCT	S	T	G	P	P
				(Marfan syndrome)
G325u3	WIAF-10114	HT0962	2022	FBN1, fibrillin 1	GATCTGCAAT[A/C]ATGGACGCTG	M	A	C	N	H
				(Marfan syndrome)
G325u4	WIAF-10116	HT0962	3603	FBN1, fibrillin 1	GAACTGCACA[G/C]ACATTGACGA	M	G	C	D	H
				(Marfan syndrome)
C325u5	WIAF-10117	HT0962	2270	FBN1, fibrillin 1	TCTGCATCAA[C/T]GGGCGTTGCG	S	C	T	N	N
				(Marfan syndrome)
G326u1	WIAF-10036	HT1009	1854	KLKB1, kallikreim	GCAAACACAA[C/T]GGAATGTGGC	S	C	T	N	N
				B plasma (Fletcher
				factor) 1
G327u1	WIAF-10052	HT1011	1599	HRG, histidine-	AAGCCAGACA[A/T]TCAGCCCTTT	M	A	T	N	I
				rich glycoprotein
G327u2	WIAF-10054	HT1011	1083	HRG, histidine-	CCACTATTGC[C/T]CATGTCCTGC	M	C	T	P	L
				rich glycoprotein
G327u3	WIAF-10055	HT1011	1140	HRG, histidine-	GCCCAAAGAC[A/G]TTCTCATAAT	M	A	G	H	R
				rich glycoprotein
G328u1	WIAF-10145	HT1087	255	SAA1, serum amyloid	GTGCCTGGGC[T/C]GCAGAAGTGA	S	T	C	A	A
				A1
G328a2	WIAF-10511	HT1087	248	SAA1, serum amyloid	CCTGGGGGTC[C/T]CTGGGCTGCA	M	C	T	A	V
				A1
G328a3	WIAF-10512	HT1087	305	SAA1, serum amyloid	TTCTTTGGCC[A/G]TGGTGCGGAC	M	A	G	H	R
				A1
G328a4	WIAF-13126	HT1087	295	SAA1, serum amyloid	TATCCAGAGA[T/C]TCTTTGGCCA	M	T	C	F	L
				A1
G328a5	WIAF-13127	HT1087	82	SAA1, serum amyloid	CTTGGTCCTG[C/A]GTGTCAGCAG	M	G	A	G	S
				A1
G329u1	WIAF-10140	HT1141	2514	PLCG1, phospho-	CTGACCTTCA[T/C]CAAGAGCGCC	M	T	C	I	T
				lipase C, gamma 1
				(formerly subtype
				148)
G329u2	WIAF-10162	HT1141	1036	PLCG1, phospho-	TATGCCCGGA[C/A]ACCATGAACA	M	C	A	D	E
				lipase C, gamma 1
				(formerly subtype
				148)
G329u3	WIAF-10163	HT1141	911	PLCG1, phospho-	GTTCATGCTC[A/G]GCTTCCTCCG	M	A	G	S	G
				lipase C, gamma 1
				(formerly subtype
				148)
G3295u1	WIAF-14017	HT3460	1229	FUBP, far upstream	CCATAAAAAG[C/T]ATAACCCAGC	S	C	T	S	S
				element binding
				protein
G3296u1	WIAF-14168	HT3466	6289	transcription	CAGCCTGGAC[G/A]AGAGCCCCAT	M	G	A	E	K
				factor TFIIIC, RNA
				polymerase III,
				alpha subunit
G3296u2	WIAF-14179	HT3466	235	transcription	GGCCATCAGC[T/A]TCTATGAGGA	M	T	A	F	I
				factor TFIIIC, RNA
				polymerase III,
				alpha subunit
G3298u1	WIAF-13523	HT3504	1803	DNA-binding protein	ACTTTGCCAA[C/T]GTGCAGGAGC	S	C	T	N	N
				HRFX2
G3298u2	WIAF-13524	HT3504	1743	DNA-binding protein	GGGCGGTGCT[G/A]CAGAACACGT	S	G	A	L	L
				HRFX2
G3298u3	WIAF-13528	HT3504	2002	DNA-binding protein	GTTCTTGCTG[A/G]AATGGTCCTT	M	A	G	K	E
				HRFX2
G33u1	WIAF-10254	X82540	1044	INHBC, inhibin,	AAGGCCAACA[C/T]AGCTGCAGGC	M	C	T	T	I
				beta C
G33u2	WIAF-10255	X82540	1136	INHBC, inhibin,	CAGCAACATT[G/A]TCAAGACTGA	M	G	A	V	I
				beta C
G33u3	WIAF-10256	X82540	1185	INHBC, inhibin,	GGGTGCAGTT[A/G]GTCTATGTGT	N	A	G	*	W
				beta C
G33u4	WIAF-10259	X82540	892	INHBC, inhibin,	TTTTTGTGGA[C/T]TTCCGTGAGA	S	C	T	D	D
				beta C
G3303u1	WIAF-13566	HT3523	981	POU6F1, POU	CAGGCCAGGA[G/A]ATCACTGAAA	S	G	A	E	E
				domain, class 6,
				transcription
				factor 1
G3304u1	WIAF-13932	HT3544	970	SP2, Sp2 transcrip-	TCAACAACCT[C/T]GTGAACGCCA	S	C	T	L	L
				tion factor
G3304u2	WIAF-13935	HT3544	1891	SP2, Sp2 transcrip-	AGAAGCACGT[T/G]TGCCACATCC	S	T	G	V	V
				tion factor
G3304u3	WIAF-13943	HT3544	920	SP2, Sp2 transcrip-	TGTGGTGAAG[T/C]TGACAGGTGG	S	T	C	L	L
				tion factor
G3311u1	WIAF-13839	HT3585	757	GATA3, GATA-	CCCACTCCCG[T/C]GGCAGCATGA	S	T	C	R	R
				binding protein 3
G3311u2	WIAF-13840	HT3585	901	GATA3, GATA-	TCGGATGCAA[G/A]TCCAGGCCCA	S	G	A	K	K
				binding protein 3
G3316u1	WIAF-13818	HT3607	282	zinc finger	AAAGAGTTTC[A/G]GTCACACTTC	M	A	G	S	G
				protein HKE-T1,
				Kruppel-like
G3319u1	WIAF-14214	HT3613	1086	SMARCA3, SWI/SNF	AAACTCTTAC[A/C]GCCATTGCAG	S	A	G	T	T
				related, matrix
				associated, actin
				dependent regulator
				of chromatin,
				subfamily a, member
				3
G3319u2	WIAF-14221	HT3613	1261	SMARCA3, SWI/SNF	TAGATCTAGT[G/C]AACAACCCAG	M	G	C	E	Q
				related, matrix
				associated, actin
				dependent regulator
				of chromatin,
				subfamily a, member
				3
G3320u1	WIAF-13692	HT3622	624	BCL6, B-cell CLL/	ATTTGCGGGA[G/C]GGCAACATCA	M	G	C	E	D
				lymphoma 6 (zinc
				finger protein 51)
G3320u2	WIAF-13717	HT3622	1062	BCL6, B-cell CLL/	ACAGCCGGCC[C/A]ACTTTGGAGG	S	G	A	P	P
				lymphoma 6 (zinc
				finger protein 51)
G3321u1	WIAF-13761	HT3641	235	STAT2, signal	TCTTGGATCA[G/C]CTGAACTATG	M	G	C	Q	H
				transducer and
				activator of
				transcription 2,
				113 kD
G3321u2	WIAF-13762	HT3641	774	STAT2, signal	CAAAAAGCCT[G/C]CATCAGAGCT	M	G	C	C	S
				transducer and
				activator of
				transcription 2,
				113 kD
G3328u1	WIAF-13543	HT3681	1550	transcription	CCACAATGGT[A/C]TCAGAGCAGG	S	A	G	V	V
				factor znf6
G3328u2	WIAF-13544	HT3681	1389	transcription	AGAGGATTTA[G/C]AGGAAGATGA	M	G	C	E	Q
				factor znf6
G3336u1	WIAF-13848	HT3732	216	XBP1, X-box binding	ACCTGAGCCC[C/T]GAGGAGAAGG	S	C	T	P	P
				protein 1
G334u1	WIAF-1008	HT1220	893	THBS1, thrombo-	TACATTCGCC[A/C]CAAGACAAAG	M	A	C	H	P
				spondin 1
G334u2	WIAF-10009	HT1220	2000	THBS1, thrombo-	TCACAGCCCT[T/C]CGGCCAGCCT	M	T	C	F	S
				spondin 1
G334u3	WIAF-10016	HT1220	1521	THBS1, thrombo-	CCCAGATGAA[T/C]GGCAAACCCT	S	T	C	N	N
				spondin 1
G334u4	WIAF-10017	HT1220	2210	THBS1, thrombo-	GGCTGGCCCA[A/G]TGAGAACCTG	M	A	G	N	S
				spondin 1
G334u5	WIAF-10018	HT1220	2979	THBS1, thrombo-	GTGAGACCGA[T/C]TTCCGCCGAT	S	T	C	D	D
				spondin 1
G334u6	WIAF-10033	HT1220	1136	THBS1, thrombo-	TGTCACTGTC[A/G]GAACTCACTT	M	A	G	Q	R
				spondin 1
G334u7	WIAF-10034	HT1220	1859	THBS1, thrombo-	AGTGGAAATG[C/A]CATCCAGTGC	M	G	A	G	D
				spondin 1
G3343u1	WIAF-13545	HT3770	1104	ZNF76, zinc finger	GCACTGCCCA[C/T]GGCGAGCTGG	S	C	T	H	H
				protein 76
				(expressed in
				testis)
G3343u2	WIAF-13561	HT3770	425	ZNF76, zinc finger	GAGCAGTATG[C/A]CAGCAAGGTT	M	C	A	A	D
				protein 76
				(expressed in
				testis)
G3343u3	WIAF-13562	HT3770	143	ZNF76, zinc finger	CACCAGGTGA[C/T]GGTACAGAAA	M	C	T	T	M
				protein 76
				(expressed in
				testis)
G3343u4	WIAF-13563	HT3770	646	ZNF76, zinc finger	GAAGACCCAC[G/T]TTCGTACCCA	M	G	T	V	F
				protein 76
				(expressed in
				testis)
G3343u5	WIAF-13564	HT3770	611	ZNF76, zinc finger	AGCTGTGGAA[A/G]GGCCTTTGCC	M	A	G	K	R
				protein 76
				(expressed in
				testis)
G3344u1	WIAF-13664	HT3772	925	zinc finger protein	AGCTCTCGCA[C/T]TCGGACGACA	S	C	T	H	H
				HAZ
G3345u1	WIAF-13508	HT3823	315	TCF6L1, transcrip-	TTCGATTTTC[T/C]AAAGAACAAC	S	T	C	S	S
				tion factor 6-
				like 1 (mito-
				chondrial
				transcription
				factor 1-like)
G3345u2	WIAF-13509	HT3823	167	TCF6L1, transcrip-	GGCGTGCTGA[G/CITGCCCTGGGA	M	G	C	S	T
				tion factor 6-
				like 1 (mito-
				chondrial
				transcription
				factor 1-like)
G3345u3	WIAF-13531	HT3623	625	TCF6L1, transcrip-	TTATAACGTT[T/G]ATGTAGCTGA	M	T	G	Y	D
				tion factor 6-
				like 1 (mito-
				chondrial
				transcription
				factor 1-like)
G3352u1	WIAF-13589	HT4005	1190	MITF, micro-	CTCGGAACTG[G/A]GACTCAGGCC	M	G	A	G	E
				phthalmia-associated
				transcription factor
G3352u2	WIAF-13604	HT4005	1156	MITF, micro-	TCTCACGGAT[G/A]GCACCATCAC	M	G	A	G	S
				phthalmia-associated
				transcription factor
G3353u1	WIAF-13937	HT4010	360	GTF2H3, general	ATCTAATGAC[C/A]AAAAGTGACA	S	C	A	T	T
				transcription
				factor IIH,
				polypeptide 3
				(34 kD subunit)
G3358u1	WIAF-13671	HT4187	398	ETV5, ets variant	GATGATGAAC[A/C]GTTTGTCCCA	M	A	G	Q	R
				gene 5 (ets-related
				molecule)
G3358u2	WIAF-13672	HT4187	223	ETV5, ets variant	TCAGCAAGTC[C/T]CTTTTATGGT	M	C	T	P	S
				gene 5 (ets-related
				molecule)
G3358u3	WIAF-13673	HT4187	1236	ETV5, ets variant	GACTGGAAGC[C/G]AAAGTCAAAC	S	C	G	G	G
				gene 5 (eta-related
				molecule)
G3358u4	WIAF-13674	HT4187	1678	ETV5, ets variant	TTACCTCCTC[G/A]ACATGGACCG	M	G	A	D	N
				gene 5 (ets-related
				molecule)
G3358u5	WIAF-13706	HT4187	414	ETV5, ets variant	TCCCAGATTT[T/C]CAGTCTGATA	S	T	C	F	F
				gene 5 (ets-related
				molecule)
G3358u6	WIAF-13707	HT4187	1238	ETV5, ets variant	CTGGAAGGCA[A/C]AGTCAAACAG	M	A	G	K	R
				gene 5 (ets-related
				molecule)
G336u1	WIAF-10152	HT1258	566	ACAT1, acetyl-	AGAGCATCTC[C/A]AATGTTCCAT	S	C	A	S	S
				Coenzyme A acetyl-
				transferase 1
				(acetoacetyl
				Coenzyme A thiolase)
G3369u1	WIAF-14047	HT4302	614	zinc finger	ATCTCAATCG[A/G]CACAAGCTCT	S	A	G	R	R
				protein DB1
G337u1	WIAF-10268	HT1259	464	EDNRB, endothelin	AAAGCAGACA[G/T]GACGGCAGGA	M	G	T	R	M
				receptor type B
G337u2	WIAF-10298	HT1259	1281	EDNRB, endothelin	TGAAGCTCAC[T/A]CTTTATAATC	S	T	A	T	T
				receptor type B
G3373u1	WIAF-14203	HT4342	1253	MTF1, metal-	CTCAACAGAC[A/G]GCTTCCTTGA	S	A	G	T	T
				regulatory
				transcription
				factor 1
G3390u1	WIAF-14182	HT4483	680	ZNF133, zinc finger	AGAGCCAGAG[C/T]TCTACCTCGA	M	C	T	L	F
				protein 133 (clone
				pHZ-13)
G3390u2	WIAF-14184	HT4483	1026	ZNF133, zinc finger	GCTCACACAG[G/A]GAACCCTGAG	M	G	A	G	E
				protein 133 (clone
				pHZ-13)
G3390u3	WIAF-14185	HT4483	1423	ZNF133, zinc finger	AAAAGCCTTA[T/C]GTGTGCCGGG	S	T	C	Y	Y
				protein 133 (clone
				pHZ-13)
G3390u4	WIAF-14197	HT4483	811	ZNF133, zinc finger	CTGGGGATCC[A/G]GGCCCAGGGG	S	A	G	P	P
				protein 133 (clone
				pHZ-13)
G3390u5	WIAF-14198	HT4483	1420	ZNF133, zinc finger	GGGAAAAGCC[T/G]TATGTCTCCC	S	T	G	P	P
				protein 133 (clone
				pHZ-13)
G3390u6	WIAF-14199	HT4483	2143	ZNF133, zinc finger	CAGCTCTAAT[C/T]ACACACAAGC	S	C	T	I	I
				protein 133
				(clone pHZ-13)
G3391u1	WIAF-13631	HT4484	391	ZNF136, zinc finger	AGCATTGTAT[A/G]TGGAGAAGTC	M	A	G	Y	C
				protein 136
				(clone pHZ-20)
G3396u1	WIAF-13978	HT4491	1283	ZNF135, zinc finger	CACACCTCCT[C/T]GCTCAGCCAG	M	C	T	S	L
				protein 135
				(clone pHZ-17)
G3396u2	WIAF-13979	HT4491	1296	ZNF135, zinc finger	TCAGCCAGCA[C/T]GAAAGGACGC	S	C	T	H	H
				protein 135
				(clone pHZ-17)
G3396u3	WIAF-13980	HT4491	1028	ZNF135, zinc finger	AGTCACAGCT[C/T]CTCCCTCACC	M	C	T	S	L
				protein 135
				(clone pHZ-17)
G3396u4	WIAF-13981	HT4491	1057	ZNF135, zinc finger	GCGAATCCAC[A/C]CTGGGGAGAA	M	A	G	T	A
				protein 135
				(clone pHZ-17)
G3396u5	WIAF-13982	HT4491	1152	ZNF135, zinc finger	CAGGAGAGAA[A/G]CCCTATGAAT	S	A	G	K	K
				protein 135
				(clone pHZ-17)
G3396u6	WIAF-13983	HT4491	1243	ZNF135, zinc finger	AAAGCCGTAT[G/C]GGTGCAATGA	M	G	C	G	R
				protein 135
				(clone pHZ-17)
G3396u7	WIAF-13984	HT4491	1045	ZNF135, zinc finger	CACCAAACAT[C/T]AGCGAATCCA	N	C	T	Q	*
				protein 135
				(clone pHZ-17)
G340u1	WIAF-10139	HT1386	459	CYP27A1, cytochrome	CCTATGGGCC[G/A]TTCACCACGG	S	G	A	P	P
				P450, subfamily
				XXVIIA (steroid 27-
				hydroxylase,
				cerebrotendinous
				xanthomatosis),
				polypeptide 1
G340u2	WIAF-10160	HT1386	801	CYP27A1, cytochrome	TCCCCAAGTG[G/A]ACTCGCCCCG	N	G	A	W	*
				P450, subfamily
				XXVIIA (steroid 27-
				hydroxylase,
				cerebrotendinous
				xanthomatosis),
				polypeptide 1
G341u1	WIAF-10121	HT1388	912	MUT, methylmalonyl	GAGCTGGCCT[A/G]TACTTTAGCA	M	A	G	Y	C
				Coenzyme A
				mutase
G341u2	WIAF-10128	HT1388	2087	MUT, methylmalonyl	TGCTCTGGGC[G/A]TAAGCACCCT	M	G	A	V	I
				Coenzyme A
				mutase
G3410u1	WIAF-13749	HT4550	1720	zinc finger	TGAGTCCTCT[G/T]TTTCATCAGC	M	G	T	V	F
				homeodomain protein
G3410u2	WIAF-13750	HT4550	2843	zinc finger	AAACATCATT[T/C]GATTGAACAC M	T	C	L	S
				homeodonain protein
G3410u3	WIAF-13751	HT4550	2745	zinc finger	AGATATTCCA[A/T]AAGAGTAGTT	M	A	T	Q	H
				homeodomain protein
G3410u4	WIAF-13775	HT4550	236	zinc finger	AGAGAAGGGA[A/C]TGCTAACAAC	M	A	C	N	T
				homeodomain protein
G3410u5	WIAF-13776	HT4550	195	zinc finger	TGCCAACAGA[C/T]CAGACAGTGT	S	C	T	D	D
				homeodomain protein
G3410u6	WIAF-13777	HT4550	606	zinc finger	ATAACTTTAG[T/C]TGCTCCCTGT	S	T	C	S	S
				homeodomain protein
G3410u7	WIAF-13793	HT4550	2073	zinc finger	CAGTTTTACC[A/C]GTGCCATCAA	S	A	G	P	P
				homeodomain protein
G343u1	WIAF-10120	HT1552	561	HK1, hexokinase 1	CTTGCCAACA[A/C]TCCAAAATAG	S	A	G	Q	Q
C343u2	WIAF-10124	HT1552	159	HK1, hexokinase 1	ACAAGTATCT[G/C]TATGCCATCC	S	G	C	L	L
G348u1	WIAF-10269	HT1906	2212	PECAM1, platelet/	TGACGATGTC[A/G]GAAACCATCC	S	A	G	G	G
				endothelial cell
				adhesion molecule
				(CD31 antigen)
G348u2	WIAF-10277	HT1906	1656	PECAM1, platelet/	GCCATTCCCA[C/T]GCCAAAATGT	S	C	T	H	H
				endothelial cell
				adhesion molecule
				(CD31 antigen)
G348u3	WIAF-10283	HT1906	577	PECAM1, platelet/	AGAGTACCAG[C/G]TGTTGGTGGA	S	C	G	V	V
				endothelial cell
				adhesion molecule
				(CD31 antigen)
G348a5	WIAF-13119	HT1906	?	PECAM1, platelet/	ATTCTTCCC[C/G]	?	C	G
				endothelial cell
				adhesion molecule
				(CD31 antigen)
G351u1	WIAF-10123	HT1990	1047	OSBP, oxysterol	TGCTCGCAGA[C/A]TCAGATGAAT	S	G	A	E	E
				binding protein
G351u2	WIAF-10132	HT1990	1023	OSBP, oxysterol	TGGCCAAGGC[C/A]AAAGCTGTGA	S	C	A	A	A
				binding protein
G355u1	WIAF-10146	HT2143	1670	THBS4,	AACTCCCTGA[C/A]TGTCTTAAAT	M	G	A	S	N
				thrombospondin 4
G355u2	WIAF-10165	HT2143	1186	THBS4,	TCGAAATCCA[G/C]CGTGCGTTCC	M	G	C	A	P
				thrombospondin 4
G355a3	WIAF-10510	HT2143	1962	THBS4,	ACTGCCCCAC[C/G]GTCATTAACA	S	C	G	T	T
				thrombospondin 4
G355a4	WIAF-13125	HT2143	1963	THBS4,	CTGCCCCACC[G/a]TCATTAACAG	M	C	a	V	I
				thrombospondin 4
G3552u1	WIAF-12701	HT28101	1006	CLCN2, chloride	AAGAGACTAT[T/C]ACAGCCCTCT	S	T	C	I	I
				channel 2
G3552u2	WIAF-12731	HT28101	1823	CLCN2, chloride	CCGCCACCAG[C/T]AGTACCCGGT	N	C	T	Q	*
				channel 2
G3552u3	WIAF-12736	HT28101	2254	CLCN2, chloride	GGAGCGCAGA[G/C]TCGGCAGGCA	M	G	C	E	D
				channel 2
G3565u1	WIAF-12744	HT2896	334	calcyclin	GCCCTCAAGG[G/A]CTGAAAATAA	M	G	A	G	D
G357u1	WIAF-10267	HT2244	4300	C4B, complement	ATGAGTACGA[T/C]GAGCTTCCAG	S	T	C	D	D
				component 4B
G357u2	WIAF-10280	HT2244	5095	C4B, complement	TCATGGGTCT[G/A]GATGGGGCCA	S	G	A	L	L
				component 4B
G357u3	WIAF-10295	HT2244	2996	C4B, complement	CTCAGATCCA[T/C]TGGACACTTT	S	T	C	L	L
				component 4B
G359u1	WIAF-10026	HT2411	936	PLAT, plasminogen	CGCAGGCTCA[A/C]GTGGGAGTAC	M	A	G	T	M
				activator, tissue
G359a2	WIAF-10520	HT2411	1444	PLAT, plasminogen	AGGCCTTGTC[T/C]CCTTTCTATT	S	T	C	S	S
				activator, tissue
G3592u1	WIAF-12759	HT4214	743	CLCN4, chloride	CTTCTAACGA[C/A]ACCACTTTTG	S	G	A	E	E
				channel 4
G3592u2	WIAF-12761	HT4214	835	CLCN4, chloride	GCTTACATTC[T/G]GAATTACTTA	M	T	G	L	R
				channel 4
G361u1	WIAF-10053	HT2479	857	cystathionine beta	TGGCTCACTA[C/T]GACACCACCG	S	C	T	Y	Y
				synthase, alt.
				transcript 1
G361u2	WIAF-10056	HT2479	1097	cystathionine beta	TCATCCCCAC[G/A]GTGCTGGACA	S	G	A	T	T
				synthase, alt.
				transcript 1
G362u1	WIAF-10058	HT2638	223	ADRB2, adrenergic,	GGCACCCAAT[G/A]GAACCCATCC	M	G	A	G	R
				beta-2-, receptor,
				surface
G362u2	WIAF-10059	HT2638	429	ADRS2, adrenergic,	TCATGGGCCT[G/A]CCAGTGGTGC	S	G	A	L	L
				beta-2-, receptor,
				surface
G362u3	WIAF-10060	HT2638	256	ADRB2, adrenergic,	CGTCACGCAG[G/C]AAAGGGACCA	M	G	C	E	Q
				beta-2-, receptor,
				surface
G362u4	WIAF-10093	HT2638	1230	ADRB2, adrenergic,	AGGCCTATGG[G/C]AATGGCTACT	S	G	C	G	G
				beta-2-, receptor,
				surface
G3620u1	WIAF-12808	HT97200	458	ACATN, acetyl-	CACTCTCTGG[A/G]TATGAAGAGC	M	A	G	D	G
				Coenzyme A
				transporter
G3627u1	WIAF-12820	HT97387	347	NAPG, N-ethyl-	GCACAAACTA[C/T]CAGAGGCCGT	M	C	T	P	S
				maleimide-sensitive
				factor attachment
				protein, gamma
G366u1	WIAF-10046	HT2764	987	BDKRB2, bradykinin	GCCTCCTTCA[T/C]CGCCTACAGC	M	T	C	M	T
				receptor B2
G366a2	WIAF-10500	HT2764	820	BDKRB2, bradykinin	AGATCCAGAC[C/A]GAGAGGAGGG	S	G	A	T	T
				receptor B2
G366a3	WIAF-10501	HT2764	961	BDKRB2, bradykinin	GCATCATCGA[T/C]GTAATCACAC	S	T	C	D	D
				receptor B2
G367u1	WIAF-10156	HT27685	6965	ACACA, acetyl-	ATCATCCATA[T/C]GACGCAGCAC	N	T	C	*	C
				Coenzyme A
				carboxylase alpha
G370u1	WIAF-10281	HT27888	3250	LEPR, leptin	AAAATTCTCC[G/A]TTGAAGGATT	S	G	A	P	P
				receptor
G370u2	WIAF-10282	HT27888	3229	LEPR, leptin	TCACCAAGTG[C/T]TTCTCTAGCA	S	C	T	C	C
				receptor
G370u3	WIAF-10284	HT27888	1005	LEPR, leptin	CAATATCAAG[T/C]GAAATATTCA	M	T	C	V	A
				receptor
G370u4	WIAF-10285	HT27888	1894	LEPR, leptin	CAGAGAATAA[C/TI CTTCAATTCC	S	C	T	N	N
				receptor
G370u5	WIAF-10299	HT27888	1222	LEPR, leptin	TTCTGACAAG[T/C]GTTGGGTCTA	S	T	C	S	S
				receptor
G370u6	WIAF-10300	HT27888	2161	LEPR, leptin	CTATGAAAAA[G/C]GAGAAAAATG	M	G	C	K	N
				receptor
G371u1	WIAF-10107	HT27943	349	CRAT, carnitine	TCATCTACTC[G/C]AGCCCAGGCG	S	G	C	S	S
				acetyltransferase
G371a2	WIAF-12093	HT27943	287	CRAT, carnitine	GGAGAACTGG[C/T]TGTCTGAGTG	S	C	T	L	L
				acetyltransferase
G372a1	WIAF-10506	HT28247	1099	HADHA, hydroxyacyl-	TGGAGCTCCA[C/A]AGAAGGATGT	M	C	A	Q	K
				Coenzyme A dehydro-
				genase dehydro-
				genase/3-ketoacyl-
				Coenzyme A
				thiolase/enoyl-
				Coenzyme A
				hydratase (tri-
				functional
				protein), alpha
				subunit
G374u1	WIAF-10103	HT28496	4435	FASN, fatty acid	CACCTCCCAC[G/A]TCCCGGAGGT	M	G	A	V	I
				synthase
G374u2	WIAF-10104	HT28496	5996	FASN, fatty acid	CTGGACAGGG[T/C]GACCCGAGAG	M	T	C	V	A
				synthase
G374u3	WIAF-10105	HT28496	5644	FASN, fatty acid	CAAGAGCTAC[A/G]TCATCGCTGG	M	A	G	I	V
				synthase
G374u4	WIAF-10115	HT28496	6387	FASN, fatty acid	TGGCACACAT[C/T]CTGGGCATCC	S	C	T	I	I
				synthase
G374u5	WIAF-10119	HT28496	567	FASN, fatty acid	GGGGCATCAA[C/T]GTCCTGCTGA	S	C	T	N	N
				synthase
G374a6	WIAF-12094	HT28496	5520	FASN, fatty acid	ACATGGCCCA[A/G]GGGAAGCACA	S	A	G	Q	Q
				synthase
G377u1	WIAF-10142	HT2996	929	PCCB, propionyl	GGACCCGGCT[T/C]CCGTCCGTGA	M	T	C	S	P
				Coenzyme A
				carboxylase,
				beta polypeptide
G377u2	WIAF-10143	HT2996	1416	PCCB, propionyl	CACCTTTGTG[G/A]TGATACCAAC	N	G	A	G	D
				Coenzyme A
				carboxylase,
				beta polypeptide
G380u1	WIAF-10122	HT3159	831	INSR, insulin	TCTACCTCCA[C/T]GGCAGGTGTG	S	C	T	D	D
				receptor
G380u2	WIAF-10126	HT3159	1698	INSR, insulin	GGCAGGATCC[A/G]TGTGGTTCCA	S	A	G	A	A
				receptor
G380u4	WIAF-11605	HT3159	2382	INSR, insulin	GCGTGCCCAC[G/A]AGTCCGGAGG	S	G	A	T	T
				receptor
G383u1	WIAF-10125	HT33546	3633	phospholipase C,	AGCAGCGGGC[G/A]AGGCTCCCCC	M	G	A	R	Q
				beta 3, alt.
				transcript 2
G385u1	WIAF-10141	HT3383	1505	PRCP,	ATGACAGTGC[A/G]GGAAAGCAGC	S	A	G	A	A
				prolylcarboxy-
				peptidase
				(angiotensinase C)
G385u2	WIAF-10157	HT3383	1360	PRCP,	ATCACAGACA[C/G]TCTGGTTGCA	M	C	G	T	S
				prolylcarboxy-
				peptidase
				(angiotensinase C)
G387u1	WIAF-11729	HT3439	2697	SREBF2, sterol	CACTCTCCAG[G/C]AGCTCCGTGC	M	G	C	R	S
				regulatory element
				binding tran-
				scription factor 2
G387u2	WIAF-11770	HT3439	1901	SREBF2, sterol	GCTGCTGCCC[C/G]CAACCTACAA	M	C	G	A	G
				regulatory element
				binding tran-
				scription factor 2
G388u1	WIAF-10270	HT3440	245	SELPLG, selectin	CTCCAGAAAT[G/A]CTGAGGAACA	M	G	A	M	I
				P ligand
G390u1	WIAF-10276	HT3568	2049	NOS3, nitric oxide	TTGCTCGTGC[C/G]GTGGACACAC	S	C	G	A	A
				synthase 3
				(endothelial cell)
G391u1	WIAF-10013	HT3630	6205	VWF, von Willebrand	AGCACCTGCA[G/C]GTGATTCTCC	M	G	C	E	D
				factor
G391u2	WIAF-10265	HT3630	4554	VWF, von Hillebrand	GCCCCTCACA[A/C]CAACGCCTTC	M	A	G	N	S
				factor
G391u3	WIAF-10266	HT3630	7489	VWF, von Willebrand	TGGCCTCAAC[C/T]GCCACCAATC	S	C	T	T	T
				factor
C391u4	HIAF-10272	HT3630	2470	VWF, von Willebrand	ACTGTACCAT[G/A]AGTGCAGTCC	M	G	A	M	I
				factor
G391u5	WIAF-10273	HT3630	2615	VWF, von Willebrand	GCTCGAGTGT[A/G]CCAAAACGTG	M	A	G	T	A
				factor
G391u6	WIAF-10274	HT3630	2635	VWF, von Willebrand	GCCAGAACTA[T/C]GACCTGGACT	S	T	C	Y	Y
				factor
G391u7	WIAF-10275	HT3630	4045	VWF, von Willebrand	TCTCGGAACC[G/A]CCGTTGCACG	S	G	A	P	P
				factor
G391u8	WIAF-10278	HT3630	4446	VWF, von Willebrand	AACTTTGTCC[C/A]CTACGTCCAG	M	G	A	R	H
				factor
G391u9	WIAF-10279	HT3630	5152	VWF, von Willebrand	GCCCTAATGC[C/T]AACGTGCACG	S	C	T	A	A
				factor
G391u10	WIAF-10286	HT3630	3448	VWF, von Willebrand	TTACCAGTGA[C/T]GTCTTCCAGG	S	C	T	D	D
				factor
G391u11	WIAF-10287	HT3630	4891	VWF, von Willebrand	ACATGGTCAC[C/T]GTGGAGTACC	S	C	T	T	T
				factor
G391u12	WIAF-10288	HT3630	4805	VWF, von Willebrand	CAGGAGCAAG[G/A]AGTTCATGGA	M	G	A	E	K
				factor
G391u13	WIAF-10289	HT3630	4943	VWF, von Willebrand	CCTGCAGCCC[G/T]TGCGAGAGAT	M	G	T	V	L
				factor
G391u14	WIAF-10290	HT3630	4915	VWF, von Willebrand	TCAGCGAGGC[A/C]CAGTCCAAAG	S	A	C	A	A
				factor
G391a15	WIAF-10517	HT3630	6194	VWF, von Willebrand	AAACAAGGAG[C/T]AGGACCTGGA	N	C	T	Q	*
				factor
G391a16	WIAF-13222	HT3630	6419	VWF, von Willebrand	TCACCTTGGT[C/T]ACATCTTCAC	M	C	T	H	Y
				factor
G3941u1	WIAF-14123	HT3464	1265	mannosidase, alpha,	CACGTCTGCA[A/G]CCAGCTGGAG	M	A	G	N	S
				lysosomal
G3941u2	WIAF-14135	HT3464	965	mannosidase, alpha,	ACCAACCACA[C/T]TGTGATGACC	M	C	T	T	I
				lysosomal
G395u1	WIAF-10271	HT4158	1627	ECE1, endothelin	TCACTGCCGA[T/C]CAGCTCAGGA	S	T	C	D	D
				converting enzyme 1
G395a2	WIAF-13110	HT4158	1493	ECE1, endothelin	CATCTACAAC[A/T]TGATAGGATA	M	A	T	M	L
				converting enzyme 1
G3959u1	WIAF-13634	HT4490	250	ADTB1, adaptin,	TGAAGAAGCT[G/A]GTATACCTCT	S	G	A	L	L
				beta 1 (beta
				prime)
G3959u2	WIAF-13640	HT4490	2029	ADTB1, adaptin,	TTCTTGGCGG[T/C]GCCCTTGACA	S	T	C	G	G
				beta 1 (beta
				prime)
G3959u3	WIAF-13641	HT4490	2395	ADTB1, adaptin,	AGGTCCACGC[C/A]CCACTCACCC	S	G	A	A	A
				beta 1 (beta
				prime)
G3967u1	WIAF-13997	HT2958	918	ACTC, actin,	GAGGCACCAC[T/C]ATGTACCCTG	S	T	C	T	T
				alpha, cardiac
				muscle
G3968u1	WIAF-14159	HT1986	1747	ACTN3, actinin,	CGAGGCTGAC[C/T]GAGAGCGAGG	N	C	T	R	*
				alpha 3
G3968u2	WIAF-14164	HT1986	1900	ACTN3, actinin,	GGTGCCCAGC[C/T]GTGACCAGAC	M	C	T	R	C
				alpha 3
G3968u3	WIAF-14165	HT1986	2184	ACTN3, actinin,	ACACCGTCTA[C/T]AGCATGGAGC	S	C	T	Y	Y
				alpha 3
G3968u4	WIAF-14167	HT1986	2557	ACTN3, actinin,	GATCTTGCCA[G/A]GAGACAAGAA	M	G	A	G	R
				alpha 3
G3968u5	WIAF-14175	HT1986	1212	ACTN3, actinin,	GGCTGCTCTC[G/A]GAGATCCGGC	S	G	A	S	S
				alpha 3
G3979u1	WIAF-13884	HT0623	776	GPC1, glypican 1	TGCTGCTGCC[T/G]GATCACTACC	S	T	G	P	P
G3979u2	WIAF-13885	HT0623	680	GPC1, glypican 1	TCTACTACCC[C/TI GCTGCCAACC	S	C	T	R	R
G3979u3	WIAF-13886	HT0623	1361	GPC1, glypican 1	AGCTGCTCTC[T/C]GAACCCAAGG	S	T	C	S	S
G3979u4	WIAF-13887	HT0623	1163	GPC1, glypican 1	ACAGTCTCAT[C/T]GGCAGCGTCC	S	C	T	I	I
G3979u5	WIAF-13888	HT0623	1670	GPC1, glypican 1	ACGCCAGTGA[C/T]GACGGCACCG	S	C	T	D	D
G3979u6	WIAF-13905	HT0623	1069	GPC1, glypican 1	CTTCCCAACC[A/T]CGCCGACCTG	M	A	T	Q	L
G3979u7	WIAF-13906	HT0623	1514	GPC1, glypican 1	TCATCCCTCA[C/T]GCCCTCCCCA	S	C	T	D	D
G3979u8	WIAF-13907	HT0623	1720	GPC1, glypican 1	GACCTCTCCC[G/C]CCCCAAGGTC	M	G	C	G	A
G3979u9	WIAF-13908	HT0623	1676	GPC1, glypican 1	CTCACCACGG[C/T]AGCGGCTCGG	S	C	T	G	G
G3979u10	WIAF-13909	HT0623	1719	GPC1, glypican 1	TGACCTCTCC[G/A]GCCGCAACGT	M	G	A	G	S
G399u1	WIAF-10102	HT48511	450	AQP3, aquaporin 3	TCTGGCACTT[T/C]GCCCACAACC	S	T	C	A	A
G399u2	WIAF-10111	HT48511	192	AQP3, aquaporin 3	CCTCCCTCCC[C/T]CAGGTTGTGC	S	C	T	A	A
G399u3	WIAF-10112	HT48511	165	AQP3, aquaporin 3	CCCTCATCCT[C/G]GTGATGTTTG	S	C	G	L	L
G3997u1	WIAF-13649	HT27682	473	MFAP2, micro-	TGTGTGCCCA[C/T]GAGGAGCTCC	S	C	T	H	H
				fibrillar-
				associated
				protein 2
G3997u2	WIAF-13650	HT27682	377	MFAP2, micro-	CCATACACAG[G/T]CCTTCCAAAC	M	G	T	R	S
				fibrillar-
				associated
				protein 2
G3997u3	WIAF-13876	HT27682	453	MFAP2, micro-	GGAGATCTGT[G/T]TTCGTACAGT	M	G	T	V	F
				fibrillar-
				associated
				protein 2
G4022u1	WIAF-14020	HT2426	240	TGM1, trans-	TGGCTGCTGT[T/C]CATGCCGAAA	M	T	C	S	P
				glutaminase 1 (K
				polypeptide epi-
				dermal type I,
				protein-glutamine-
				gamma glutamyl-
				transferase)
G4022u2	WIAF-14021	HT2426	371	TGM1, trans-	CCCGGGGCAG[C/TI GGTGTCAATG	S	C	T	S	S
				glutaminase 1 (K
				polypeptide epi-
				dermal type I,
				protein-glutamine-
				gamma-glutamyl-
				transferase)
G4022u3	WIAF-14022	HT2426	506	TGM1, trans-	ACGAGCTGAT[A/GIGTGCGCCGCG	M	A	G	I	M
				glutaminase 1 (K
				polypeptide epi-
				dermal type I,
				protein-glutamine-
				gamma-glutamyl-
				transferase)
G4022u4	WIAF-14031	HT2426	2491	TGM1, trans-	GGTGGAGGTG[A/T]CAGTCACTTA	M	A	T	D	V
				glutaminase 1 (K
				polypeptide epi-
				dermal type I,
				protein-glutamine-
				gamma-glutamyl-
				transferase)
G4038u1	WIAF-13998	HT4211	411	LAMB3, laminin,	GGTGGCAGTC[C/A]CAGAATGATG	S	C	A	S	S
				beta 3 (nicein
				(125 kD), kalinin
				(140 kD), BM600
				(125 kD))
G4038u2	WIAF-13999	HT4211	258	LAMB3, laminin,	CTTCATCTAC[C/T]TGTGGACTGA	S	C	T	T	T
				beta 3 (nicein
				(125 kD), kalinin
				(140 kD), BM600
				(125 kD))
G4038u3	WIAF-14002	HT4211	1830	LAMB3, laminin,	GAGGCTACTG[C/T]AATCGCTACC	S	C	T	C	C
				beta 3 (nicein
				(125 kD), kalinin
				(140 kD), BM600
				(125 kD))
G4038u4	WIAF-14003	HT4211	2668	LAMB3, laminin,	GACCACGCAG[A/T]TGATTAGGCC	M	A	T	M	L
				beta 3 (nicein
				(125 kD), kalinin
				(140 kD), BM600
				(125 kD))
G4038u5	WIAF-14018	HT4211	248	LAMB3, laminin,	TTTCTCCGAG[C/T]TTCATCTACC	M	C	T	A	V
				beta 3 (nicein
				(125 kD), kalinin
				(140 kD), BM600
				(125 kD))
G4038u6	WIAF-14019	HT4211	887	LAMB3, laminin,	CACGGCCATG[C/T]TGATCGCTGC	M	C	T	A	V
				beta 3 (nicein
				(125 kD), kalinin
				(140 kD), BM600
				(125 kD))
G4038u7	WIAF-14023	HT4211	1266	LAMB3, laminin,	AGTGTGATCC[G/A]GATGGGGCAG	S	G	A	P	P
				beta 3 (nicein
				(125 kD), kalinin
				(140 kD), BM600
				(125 kD))
G4038u8	WIAF-14025	HT4211	1693	LAMB3, laminin,	CTATGGAGAC[G/A]TGGCCACAGG	M	G	A	V	M
				beta 3 (nicein
				(125 kD), kalinin
				(140 kD), BM600
				(125 kD))
G4038u9	WIAF-14026	HT4211	1553	LAMB3, laminin,	GGCTGTGAAC[C/T]GTGTGCCTGC	M	C	T	P	L
				beta 3 (nicein
				(125 kD), kalinin
				(140 kD), BM600
				(125 kD))
G4038u10	WIAF-14029	HT4211	3562	LANB3, laminin,	CCTGACAGGA[C/T]TGGAGAAGCG	S	C	T	L	L
				beta 3 (nicein
				(125 kD), kalinin
				(140 kD), BM600
				(125 kD))
G4038u11	WIAF-14030	HT4211	3546	LAMB3, laminin,	TGCTGCGCTC[A/G]GCGGACCTGA	S	A	G	S	S
				beta 3 (nicein
				(125 kD), kalinin
				(140 kD), BM600
				(125 kD))
G4045u1	WIAF-13571	HT0652	1266	adducin, beta sub-	TGGAGCAGGA[G/T]AAGCACCGGC	M	G	T	E	D
				unit
G4050u1	WIAF-14106	HT1466	1366	villin	CGTTTGCCAG[G/A]GCAGCCAGGC	M	G	A	G	S
G4050u2	WIAF-14107	HT1466	1468	villin	GGTCCCAATG[G/A]GCAAGGAGCC	M	G	A	G	S
G4050u3	WIAF-14108	HT1466	1932	villin	CCACAGAGAT[C/T]CCTGACTTCA	S	C	T	I	I
G4050u4	WIAF-14110	HT1466	2438	villin	TTTGGGATGA[C/T]TCCACCTGCC	M	C	T	T	I
G4057u1	WIAF-13648	HT33633	371	CNN3, calponin 3,	TTCAGGCTTA[T/C]GGTATGAAGC	S	T	C	Y	Y
				acidic
G4066u1	WIAF-13676	HT4301	654	troponin T, beta,	AGATTGACAA[G/A]TTCGACTTTG	S	G	A	K	K
				skeletal
G4066u2	WIAF-13677	HT4301	774	troponin T, beta,	GCAAAGTCGG[C/T]GCGCGCTGGA	S	C	T	G	G
				skeletal
G4066u3	WIAF-13708	HT4301	625	troponin T, beta,	GGAGCTCTGG[G/C]AGACCCTGCA	M	G	C	E	Q
				skeletal
G4080u1	WIAF-14142	HT1396	13130	HSPG2, heparan	GATTCTCCTC[G/A]GCCATCACAC	S	G	A	S	S
				sulfate proteo-
				glycan 2 (perlecan)
G4080u2	WIAF-14150	HT1396	10340	HSPG2, heparan	TTGAGTTCCA[C/T]TGTCCTCTGC	S	C	T	H	H
				sulfate proteo-
				glycan 2 (perlecan)
G4080u3	WIAF-14151	HT1396	12392	HSPG2, heparan	AATGCTATGA[T/C]AGCTCCCCAT	S	T	C	D	D
				sulfate proteo-
				glycan 2 (perlecan)
G4080u4	WIAF-14152	HT1396	3416	HSPG2, heparan	TCCCTCTGCC [C/T]GAGCAAACCG	S	C	T	P	P
				sulfate proteo-
				glycan 2 (perlecan)
G4080u5	WIAF-14154	HT1396	4588	HSPG2, heparan	GTGCCGCTGG[T/C]GGCCAGCATC	M	T	C	V	A
				sulfate proteo-
				glycan 2 (perlecan)
G4080u6	WIAF-14156	HT1396	9582	HSPG2, heparan	GCACAGCCAC[C/A]CCGTGCTGCA	M	G	A	A	T
				sulfate proteo-
				glycan 2 (perlecan)
G4096u1	WIAF-13890	HT4237	394	motor protein	CAAAGAAATC[G/A]ATTCAGTCGC	S	G	A	S	S
G4096u2	WIAF-13910	HT4237	455	motor protein	ATCTAAACAC[C/T]CTGCCTCACA	M	C	T	P	S
G4096u3	WIAF-13911	HT4237	1150	motor protein	CTAACCTTGT[A/G]TCTCAGTATC	S	A	G	V	V
G4109u1	WIAF-14034	HT28223	1238	phosphoglucomutase-	TACACCGTCC[C/T]GAAGACGCAT	M	C	T	A	V
				related protein
G4109u2	WIAF-14035	HT28223	1043	phosphoglucomutase-	ATTATTCCTG[C/A]CCGGAACCAG	M	C	A	A	D
				related protein
G4112u1	WIAF-13615	HT4401	374	KIF5A, kinesin	AGATGTCCTT[G/A]CTCGCTACAA	M	G	A	A	T
				family member 5A
G4112u2	WIAF-13623	HT4401	2767	KIF5A, kinesin	AGAGAGTTAA[G/T]GCCCTCCACC	M	G	T	K	N
				family member 5A
G4114u1	WIAF-14113	HT4160	830	fibrinogen-like	AACTTCACCA[G/A]AACATGGCAA	M	G	A	R	K
				protein pT49
G4118u1	WIAF-14010	HT0841	564	MYL5, myosin,	TCGATGTGGC[G/A]GGCAACCTGG	S	G	A	A	A
				light polypeptide
				5, regulatory
G4118u2	WIAF-14011	HT0841	368	MYL5, myosin,	TTCACCATGT[T/C]TCTGAACCTG	M	T	C	F	S
				light polypeptide
				5, regulatory
G4118u3	WIAF-14012	HT0841	533	MYL5, myosin,	GAGGTGGACC[A/G]GATGTTCCAG	M	A	G	Q	R
				light polypeptide
				5, regulatory
G4122u1	WIAF-13955	HT97538	161	myosin-I	TCGAGAACCT[A/G]CGCCCCCGAT	S	A	G	L	L
G4124u1	WIAF-13895	HT0925	1517	TCM3, transgluta-	TCGCTCGCAT[G/A]CTGGCACTAG	M	G	A	M	I
				minase 3 (E poly-
				peptide, protein-
				glutamine gamma-
				glutamyl-
				transferase)
G4124u2	WIAF-13896	HT0925	1433	TCM3, transgluta-	AACCCAACAC[G/A]CCATTTGCCC	S	G	A	T	T
				minase 3 (E poly-
				peptide, protein-
				glutamine-gamma-
				glutamyl-
				transferase)
G4126u1	WIAF-13830	HT2465	1035	myosin binding	ACTCGTACTC[C/G]TTCCGGCTCT	S	C	G	S	S
				protein H
G4126u2	WIAF-13853	HT2465	369	myosin binding	AGAGAGGCAC[G/C]CTCGGAGTGG	M	G	C	G	A
				protein H
G4130u1	WIAF-13614	HT1657	198	CFL1, cofilin 1	CTGTCCACGA[T/C]CCCTACGCCA	S	T	C	D	D
				(non-muscle)
G4138u1	WIAF-13598	HT33664	601	MAGP2: Microfibril-	GAAAGATGAG[C/T]TTTCCCGTCA	M	C	T	L	F
				associated glyco-
				protein-2
G4138u2	WIAF-13599	HT33664	405	MAGP2: Microfibril-	ATGACTTGGC[C/T]TCCCTCAGTC	S	C	T	A	A
				associated glyco-
				protein-2
G4138u3	WIAF-13600	HT33664	327	MAGP2: Microfibril-	AAGATCCTAA[T/C]CTGCTGAATG	S	T	C	N	N
				associated glyco-
				protein-2
G4159u1	WIAF-14048	HT3443	1119	SNL, singed	GCTGCTACTT[T/C]GACATCGACT	S	T	C	F	F
				(Drosophila)-like
				(sea urchin fascin
				homolog like)
G4170u1	WIAF-13580	HT5069	1131	Golgi protein,	GAAATATACC[A/G]TAAGTATCGA	M	A	G	I	V
				peripheral,
				brefeldin A-
				sensitive
G4170u2	WIAF-13581	HT5069	930	Golgi protein,	GTATAATAAA[C/T]TCCTGGACTT	M	C	T	L	F
				peripheral,
				brefeldin A-
				sensitive
G4170u3	WIAF-13582	HT5069	2312	Golgi protein,	AGCAGCCTTA[A/G]GCATCTTGGA	N	A	G	*	*
				peripheral,
				brefeldin A-
				sensitive
G4170u4	WIAF-13596	HT5069	359	Golgi protein,	TCAACCACGT[T/G]TCTGTGCCTT	S	T	G	L	L
				peripheral,
				brefeldin A-
				sensitive
G4170u5	WIAF-13597	HT5069	1007	Golgi protein,	AAAAAGCCAA[T/A]ACTGTTCCTG	M	T	A	N	K
				peripheral,
				brefeldin A-
				sensitive
G4171u1	WIAF-13688	HT1587	667	KIF5B, kinesin	TTTTTAATTA[T/C]ATTTACTCCA	S	T	C	Y	Y
				family member 5B
G4171u2	WIAF-13689	HT1587	1036	KIF5B, kinesin	TTAGTAAAAC[T/C]GGAGCTGAAG	S	T	C	T	T
				family member SB
G4176u1	WIAF-14204	HT33754	130	TNR, tenascin R	GCTCATTGGC[G/A]TCAACCTGAT	M	G	A	V	I
				(restrictin,
				janusin)
G4176u2	WIAF-14205	HT33754	463	TNR, tenascin R	CTGTCCATGT[G/T]CCAGTTCAGC	M	G	T	A	S
				(restrictin,
				janusin)
G4176u3	WIAF-14206	HT33754	249	TNR, tenascin R	ACTACAACAC[G/A]TCCAGCAAAC	S	G	A	T	T
				(restrictin,
				janusin)
G4176u4	WIAF-14208	HT33754	2009	TNR, tenascin R	CTGGTCCCCA[G/A]CGCCATTGGT	M	G	A	R	K
				(restrictin,
				janusin)
G4176u5	WIAF-14209	HT33754	2175	TNR, tenascin R	CAGCCTCCTC[G/A]GAGACCTCCA	S	G	A	S	S
				(restrictin,
				janusin)
G4176u6	WIAF-14210	HT33754	3318	TNR, tenascin R	AATCCACCGA[C/T]GGAAGCCGCA	S	C	T	D	D
				(restrictin,
				janusin)
G4176u7	WIAF-14211	HT33754	3221	TNR, tenascin R	CCGGCAAACC[T/C]GACAGCCAGT	M	T	C	L	P
				(restrictin,
				janusin)
G4176u8	WIAF-14217	HT33754	1635	TNR, tenascim R	TCTCGGACAC[C/TI GTGGCTTTTG	S	C	T	T	T
				(restrictin,
				janusin)
G4178u1	WIAF-14138	HT0224	2827	ACTN2, actinin,	GCTGCGTTCT[C/T]TTCCGCACTC	M	C	T	S	F
				alpha 2
G4178u2	WIAF-14139	HT0224	2818	ACTN2, actinin,	CTGGATTACG[C/T]TGCGTTCTCT	M	C	T	A	V
				alpha 2
G418u1	WIAF-11750	L07594	2370	TGFBR3, trans-	GAGTGCACTT[C/T]CCTATCCCGC	S	C	T	F	F
				forming growth
				factor, beta
				receptor III
				(betaglycan, 300 kD)
G418u2	WIAF-11751	L07594	2586	TGFBR3, trans-	AGAAGACGTT[C/T]ACCAACCCCC	S	C	T	F	F
				forming growth
				factor, beta
				receptor III
				(betaglycan, 300 kD)
G418u3	WIAF-11752	L07594	2671	TGFBR3, trans-	AATTTCTCCA[C/T]CAATTTTCCA	M	C	T	P	S
				forming growth
				factor, beta
				receptor III
				(betaglycan, 300 kD)
G418u4	WIAF-11771	L07594	438	TGFBR3, trans-	TGTCTGAACT[C/T]TCACCTCTCA	S	G	T	L	L
				forming growth
				factor, beta
				receptor III
				(betaglycan, 300 kD)
G418u5	WIAF-11744	L07594	392	TGFBR3, trans-	CTGATCAGCT[T/C]CTGTTTAGCC	M	T	C	F	S
				forming growth
				factor, beta
				receptor III
				(betaglycan, 300 kD)
G418u6	WIAF-11772	L07594	1470	TGFBR3, trans-	AGCTACGGAT[C/T]CTGCTGGACC	S	C	T	I	I
				forming growth
				factor, beta
				receptor III
				(betaglycan, 300 kD)
G418u7	WIAF-11773	L07594	1170	TGFBR3, trans-	TCTTGAAGTG[C/A]AAAAACTCTG	N	C	A	C	*
				forming growth
				factor, beta
				receptor III
				(betaglycan, 300 kD)
G418u8	WIAF-11745	L07594	1463	TGFBR3, trans-	CCTCCTGAGC[T/C]ACGGATCCTC	M	T	C	L	P
				forming growth
				factor, beta
				receptor III
				(betaglycan, 300 kD)
G418u9	WIAF-11746	L07594	2211	TGFBR3, trans-	ATGTTGAGGT[A/G]TCTGTTACTA	S	A	G	V	V
				forming growth
				factor, beta
				receptor III
				(betaglycan, 300 kD)
G4181u1	WIAF-14207	HT2008	425	SPTBN1, spectrin,	CTCTGCGCGG[C/T]TTTTTCAGCG	M	C	T	L	F
				beta, non-
				erythrocytic 1
G4181u2	WIAF-14213	HT2008	3565	SPTBN1, spectrin,	ACACAGCGAT[C/T]GCCTCGGAGG	S	C	T	I	I
				beta, non-
				erythrocytic 1
G4181u3	WIAF-14218	HT2008	1258	SPTBN1, spectrin,	ACCTTCTGGA[A/G]TGCATTGAAC	S	A	G	E	E
				beta, non-
				erythrocytic 1
G4181u4	WIAF-14219	HT2008	1780	SPTBN1, spectrin,	AGCTCGAGGC[C/T]GAGAATTACC	S	C	T	A	A
				beta, non-
				erythrocytic 1
G4181u5	WIAF-14220	HT2006	3637	SPTBN1, spectrin,	ACATCAAGAA[T/C]GAGATCGACA	S	T	C	N	N
				beta, non-
				erythrocytic 1
G4183u1	WIAF-13976	HT2640	404	TPM4, tropomyosin 4	CCAAGCACAT[T/C]GCGGAAGAGG	S	T	C	I	I
G4185u1	WIAF-13554	HT3451	257	MFAP1, micro-	AAGGCCAGAC[T/C]ATGCCCCTAT	M	T	G	Y	D
				fibrillar-
				associated
				protein 1
G4185u2	WIAF-13555	HT3451	1108	MFAP1, micro-	CCAACAAAGC[T/C]GTTAAGGGCA	S	T	G	A	A
				fibrillar-
				associated
				protein 1
G4185u3	WIAF-13570	HT3451	274	MFAP1, micro-	CTATGCAGTC[C/T]TCAGATCACG	S	C	T	S	S
				fibrillar-
				associated
				protein 1
G4196u1	WIAF-13665	HT97558	941	NUP88, nucleoporin	GGGTCCATTG[C/A]CCATGCATCT	M	C	A	A	D
				88 kD
G4196u2	WIAF-13666	HT97558	1092	NUP8B, nucleoporin	ATGACCACAC[G/A]TCAGAAAACT	S	G	A	T	T
				88 kD
G4196u3	WIAF-13667	HT97558	1551	NUP88, nucleoporin	TCCATCCAGC[C/A]TCTCCTCCCC	S	G	A	A	A
				88 kD
G4196u4	WIAF-13668	HT97558	2220	NUP88, nucleoporin	AGGGTGAACA[T/C]ATAAGCCAAA	S	T	C	H	H
				88 kD
G4196u5	WIAF-13669	HT97558	2205	NUP88, nucleoporin	CCATCCTGAA[A/G]GAGGAGGGTG	S	A	G	K	K
				88 kD
G4208u1	WIAF-13921	HT1122	1329	VCL, vinculin	TCATCCTAAA[G/C]AAAGAGATCA	M	G	C	E	Q
G4208u2	WIAF-13922	HT1122	2438	VCL, vinculin	CCATCTCCCC[A/G]ATGGTGATGC	S	A	G	P	P
G4208u3	WIAF-13941	HT1122	818	VCL, vinculin	GCCATCAAGA[T/C]GCCTGCGCCA	S	T	C	D	D
G4208u4	WIAF-13942	HT1122	1556	VCL, vinculin	AACCACAGCG[C/A]TCGATTGATA	S	G	A	R	R
G4213u1	WIAF-13605	HT2813	163	NUP153, nucleoporin	GCCAGGCTCC[T/C]TACAAAGATA	S	T	C	L	L
				153 kD
G4213u2	WIAF-13606	HT2813	742	NUP153, nucleoporin	GAATTCTTCA[A/C]TCCTTAAAAC	M	A	G	I	V
				153 kD
G4213u3	WIAF-13609	HT2813	1800	NUP153, nucleoporin	TTACACCTGC[A/C]GAAATCCTCA	S	A	C	A	A
				153 kD
G4213u4	WIAF-13627	HT2813	1829	NUP153,nucleoporin	AGTGTTCTAG[A/C]TATTCTCAAA	M	A	C	D	A
				153 kD
G4213u5	WIAF-13632	HT2813	3258	NUP153, nucleoporin	CTTTTCCCAA[C/T]GTGGAGCCTC	S	C	T	N	N
				153 kD
G4213u6	WIAF-13635	HT2813	4162	NUP153, nucleoporin	CTCTGCAACA[A/C]CTCCTAATTC	M	A	G	T	A
				153 kD
G4218u1	WIAF-13854	HT1681	1122	phosphatidyl-	AACCTTATTA[T/C]TTTATCTCAC	M	T	C	I	T
				inositol glycan,
				class A
G4223u1	WIAF-14160	HT1684	1434	CD36L2, CD36	ATTAGATGAC[T/C]TTGTTGAAAC	M	T	C	F	L
				antigen (collagen
				type I receptor,
				thrombospondin
				receptor)-like 2
				(lysosomal integral
				membrane protein
				II)
G4223u2	WIAF-14173	HT1684	696	CD36L2, CD36	GTGGTCCCAC[G/A]TGCACTTCCT	M	G	A	V	M
				antigen (collagen
				type I receptor,
				thrombospondin
				receptor)-like 2
				(lysosomal integral
				membrane protein
				II)
G4223u3	WIAF-14174	HT1684	986	CD36L2, CD36	CAGACAAGTC[C/T]AATATCATTA	S	C	T	C	C
				antigen (collagen
				type I receptor,
				thrombospondin
				receptor)-like 2
				(lysosomal integral
				membrane protein
				II)
G4223u4	WIAF-14176	HT1684	1437	CD36L2, CD36	AGATGACTTT[G/A]TTGAAACGCG	M	G	A	V	I
				antigen (collagen
				type I receptor,
				thrombospondin
				receptor)-like 2
				(lysosomal integral
				membrane protein
				II)
G4227u1	WIAF-14056	HT1929	912	proteoglycan 2	ATCCCTCCAA[C/A]AAACATCCCC	S	C	A	K	K
G4227u2	WIAF-14057	HT1929	1254	proteoglycan 2	CGAACTTTCC[C/A]TACTCCCCTC	S	C	A	A	A
G4227u3	WIAF-14058	HT1929	1321	proteoglycan 2	CCCAGCACCC[T/C]ACTCCCCTCC	M	T	C	Y	H
G4229u1	WIAF-13961	HT1689	74	SDC4, syndecan 4	CCTGCTCCTC[T/C]TCTTCCTACC	M	T	C	F	L
				(amphiglycan,
				ryudocan)
G4230u1	WIAF-13525	HT4995	602	TRAM protein	CCATAACCTC[A/C]TGACATTTCA	M	A	C	M	L
G4243u1	WIAF-14169	HT2901	406	KRT17, keratin 17	ACCTCCACCT[C/A]AACATCCCTC	S	G	A	V	V
G4243u2	WIAF-14170	HT2901	478	KRT17, keratin 17	ACACCACAAT[T/C]CACCACCTCC	S	T	C	I	I
G4243u3	WIAF-14171	HT2901	389	KRT17, keratin 17	GGAGGAGGCC[A/C]ACACTGAGCT	M	A	G	N	D
G4243u4	WIAF-14178	HT2901	564	KRT17, keratin 17	CTGGCTGCTC[A/C]TGACTTCCGC	M	A	C	D	A
G4244u1	WIAF-14086	HT1056	386	clathrin, light	ATCGATTGCA[G/C]TCAGAGCCTG	M	G	C	Q	H
				polypeptide a
G4246u1	WIAF-14044	HT97492	259	SLN, sarcolipin	GTCCTATCAC[T/C]ACTGAGAGGC	M	T	C	Y	H
G4246u2	WIAF-14045	HT97492	189	SLN, sarcolipin	ACACCCGGGA[G/A]CTGTTTCTCA	S	G	A	E	E
G4254u1	WIAF-13546	HT3393	86	TNNI2, troponin I,	ACCTGAAGAG[C/T]CTGATCCTGC	S	C	T	S	S
				skeletal, fast
G4254u2	WIAF-13553	HT3393	530	TNNI2, troponin I,
				skeletal, fast	TCGAGGAGAA[G/C]TCTGGCATGG	M	G	C	K	N
G4255u1	WIAF-13644	HT2907	562	CRYAB, crystallin,	AGTTCCACAG[G/A]AAATACCGGA	S	G	A	R	R
				alpha B
G4255u2	WIAF-13645	HT2907	367	CRYAB, crystallin,	CCTCCTTCCT[G/A]CGGCCACCCA	S	G	A	L	L
				alpha B
G4255u3	WIAF-13872	HT2907	271	CRYAB, crystallin,	CCAGCCGCCT[C/T]TTTGACCAGT	S	C	T	L	L
				alpha B
G4255u4	WIAF-13873	HT2907	580	CRYAB, crystallin,	GGATCCCAGC[T/C]GATGTAGACC	S	T	C	A	A
				alpha B
G4257u1	WIAF-14052	HT1694	394	PIGF,	TAGAGTTGGC[A/G]TTGGAAACAT	S	A	G	A	A
				phosphatidylinositol
				glycan, class F
G4257u2	WIAF-14053	HT1694	252	PIGF,	TATTTAGTAG[T/C]GAAACCAAAT	M	T	C	V	A
				phosphatidylinositol
				glycan, class F
G4257u3	WIAF-14069	HT1694	291	PIGF,	TCATTATCAC[A/G]CAAGGTAACT	M	A	G	H	R
				phosphatidylinositol
				glycan, class F
G4264u1	WIAF-13519	HT0968	1720	TJP1, tight	CGGTCAGTGG[C/T]TTCCAGCCAG	M	C	T	A	V
				junction protein 1
				(zona occludens 1)
G4264u2	WIAF-13520	HT0968	2272	TJP1, tight	CATGCTGATG[A/C]TCACACACCT	M	A	G	D	G
				junction protein 1
				(zona occludens 1)
G4264u3	WIAF-13529	HT0968	5408	TJP1, tight	AGCCTCCTGA[A/T]GCTGATGGTG	M	A	T	E	D
				junction protein 1
				(zona occiudens 1)
G434u1	WIAF-11748	M21121	286	SCYA5, small	TACATCAACT[C/T]TTTGGAGATG	M	C	T	S	F
				inducible cytokine
				A5 (RANTES)
G434u2	WIAF-11749	M21121	137	SCYA5, small	GCTTTGCCTA[C/T]ATTGCCCGCC	S	C	T	Y	Y
				inducible cytokine
				A5 (RANTES)
G435u1	WIAF-11741	M31933	754	FCGR2B, Fc fragment	GTCACTGGGA[T/C]TGCTGTAGCC	M	T	C	I	T
				of IgG, low
				affinity IIb,
				receptor for (CD32)
G435u2	WIAF-11743	M31933	395	FCGR2B, Fc fragment	GGGAGTACAC[G/A]TGCCAGACTG	S	G	A	T	T
				of IgG, low
				affinity IIb,
				receptor for (CD32)
G435u3	WIAF-11742	M31933	673	FCGR2B, Fc fragment	TACACGCTGT[T/A]CTCATCCAAG	M	T	A	F	Y
				of IgG, low
				affinity IIb,
				receptor for (CD32)
G4369u1	WIAF-13728	HT0900	1176	GBE1, glucan	TTACGTCCAT[G/A]CTTTATCATC	M	G	A	M	I
				(1,4-alpha-),
				branching enzyme 1
				(glycogen branching
				enzyme, Andersen
				disease, glycogen
				storage disease
				type IV)
G4369u2	WIAF-13729	HT0900	1609	GBE1, glucan	GAGTGTCCTG[A/G]CTCCTTTTAC	M	A	G	T	A
				(1,4-alpha-),
				branching enzyme 1
				(glycogen branching
				enzyme, Andersen
				disease, glycogen
				storage disease
				type IV)
G4373u1	WIAF-13559	HT0940	1117	HSD17B2, hydroxy-	GCCAGCAAGG[A/T]CTTCTCTCCG	M	A	T	D	V
				steroid (17-beta)
				dehydrogenase 2
G4373u2	WIAF-13560	HT0940	1195	HSD17B2, hydroxy-	CCAGGGAAAG[G/A]CGCTTACTTG	M	G	A	G	D
				steroid (17-beta)
				dehydrogenase 2
G438u1	WIAF-11830	M63121	583	TNFRSF1A, tumor	ACCGTGTGTG[G/A]CTGCAGGAAG	M	G	A	G	D
				necrosis factor
				receptor super-
				family, member 1A
G438u2	WIAF-11790	M63121	618	TNFRSF1A, tumor	TTATTGGACT[G/A]AAAACCTTTT	M	G	A	E	K
				necrosis factor
				receptor super-
				family, member 1A
G440u1	WIAF-11806	M74447	261	TAP2, transporter	TGCTAAAGCT[A/G]AGAGGGCTGC	S	A	G	L	L
				2, ABC (ATP
				binding cassette)
G440u2	WIAF-11807	M74447	2089	TAP2, transporter	CAGGCTGCAG[G/A]CAGTTCAGCG	M	G	A	A	T
				2, ABC (ATP
				binding cassette)
G440u3	WIAF-11808	M74447	2155	TAP2, transporter	TGCCCAGCTC[C/T]AGGAGGGACA	N	C	T	Q	*
				2, ABC (ATP
				binding cassette)
G440u4	WIAF-11818	M74447	1789	TAP2, transporter	GAACAACATT[G/A]CTTATGGGCT	M	G	A	A	T
				2, ABC (ATP
				binding cassette)
G440u5	WIAF-11819	M74447	1565	TAP2, transporter	AAGGGGCTGA[C/T]GTTTACCCTA	M	C	T	T	M
				2, ABC (ATP
				binding cassette)
G440u6	WIAF-11820	M74447	1254	TAP2, transporter	TGCACTTGGG[G/T[GTCCACATCC	S	C	T	G	G
				2, ABC (ATP
				binding cassette)
G440u7	WIAF-11788	M74447	1231	TAP2, transporter	GTACCTGCTC[A/C]TAACCAGGCT	M	A	G	I	V
				2, ABC (ATP
				binding cassette)
G440u8	WIAF-11821	M74447	1404	TAP2, transporter	TGCTCAGCAA[C/T]GTGGGAGCTC	S	C	T	N	N
				2, ABC (ATP
				binding cassette)
G440u9	WIAF-11783	M74447	2187	TAP2, transporter	CCCGCCTGGT[T/C]CAGCACCGGC	S	T	G	V	V
				2, ABC (ATP
				binding cassette)
G440u10	WIAF-11786	M74447	1825	TAP2, transporter	TGATAAGGTG[A/G]TGGCGGCTGC	M	A	G	M	V
				2, ABC (ATP
				binding cassette)
G4400u1	WIAF-14007	HT97396	839	A33	GCCAATCAAA[G/T]GACGGCTCAC	M	G	T	K	N
G4404u1	WIAF-14013	HT1215	109	ACP2, acid	CCGCCCACCC[G/A]GGCCCGGAGT	M	G	A	R	Q
				phosphatase 2,
				lysosomal
G4404u2	WIAF-14016	HT1215	1271	ACP2, acid	ACCGCCACGT[C/T]GCAGATGGGG	S	C	T	V	V
				phosphatase 2,
				lysosomal
G4406u1	WIAF-13661	HT3564	872	ACPP, acid	ACAAAAAACT[T/C]ATCATGTATT	S	T	C	L	L
				phosphatase,
				prostate
G4406u2	WIAF-13662	HT3564	839	ACPP, acid	ATCACATGAA[G/A]AGAGCAACTC	S	G	A	K	K
				phosphatase,
				prostate
G4406u3	WIAF-13881	HT3564	741	ACPP, acid	AGAATTGTCA[G/T]AATTGTCCCT	N	G	T	E	*
				phosphatase,
				prostate
G441u1	WIAF-10166	M77349	698	TGFBI, transforming	GTGCCCGGCT[C/G]CTGAAAGCCG	S	C	G	L	L
				growth factor,
				beta-induced, 68 kD
G441u2	WIAF-10168	M77349	1028	TGFBI, transforming	GCCTCTCTGT[A/G]CAGACCCTGG	S	A	G	V	V
				growth factor,
				beta-induced, 68 kD
G441u3	WIAF-10169	M77349	1667	TGFBI, transforming	ACACAGTCTT[T/C]GCTCCCACAA	S	T	C	F	F
				growth factor,
				beta-induced, 68 kD
G441u4	WIAF-10171	M77349	1463	TGFBI, transforming	GTAATAGCCT[C/T]TGCATTGAGA	S	C	T	L	L
				growth factor,
				beta-induced, 68 kD
G4411u1	WIAF-14005	HT97468	492	acyl-CoA	GCTCACCAAT[A/G]AGGCCACCCT	M	A	G	K	E
G4411u2	WIAF-14008	HT97468	1076	acyl-CoA	TGCCCCACAC[C/T]GAGGACGAGA	S	C	T	T	T
G4412u1	WIAF-13576	HT1882	657	ACADS, acyl-	GCAAAACAAG[G/A]GCATCAGTGC	M	G	A	G	S
				Coenzyne A
				dehydrogenase, C-2
				to C-3 short chain
G4412u2	WIAF-13579	HT1882	1022	ACADS, acyl-	TGACCTGGCC[C/T]GCTGCCATGC	S	C	T	R	R
				Coenzyme A
				dehydrogenase, C-2
				to C-3 short chain
G4415u1	WIAF-14080	HT2503	2170	acyl-Coenzyme A:	TCATTATATT[C/T]GAGCAGATTC	S	C	T	F	F
				cholesterol
				acyltransferase
G4415u2	WIAF-14081	HT2503	1993	acyl-Coenzyme A:	TTTCAGTTCC[C/T]TATTTTCTGT	S	C	T	P	P
				cholesterol
				acyltransferase
G4415u3	WIAF-14098	HT2503	2006	acyl-Coenzyme A:	TTTTCTGTTT[C/G]AACATTGGCG	M	C	G	Q	E
				cholesterol
				acyltransferase
G4415u4	WIAF-14101	HT2503	2365	acyl-Coenzyme A:	GGGGTTATGT[C/T]GCTATGAAGT	S	C	T	V	V
				cholesterol
				acyltransferase
G4417u1	WIAF-13819	HT0542	356	AOAH, acyloxyacyl	TCCAGCCAAC[G/A]ATGACCAGTC	M	G	A	D	N
				hydrolase (neutro-
				phil)
G4417u2	WIAF-13820	HT0542	340	AOAH, acyloxyacyl	TTCAGTCCTC[G/A]GCCTCTCCAG	S	G	A	S	S
				hydrolase
				(neutrophil)
G4417u3	WIAF-13824	HT0542	1595	AOAH, acyloxyacyl	GCTAAATAAA[G/A]ACATGACCTA	M	G	A	D	N
				hydrolase
				(neutrophil)
G4417u4	WIAF-13841	HT0542	382	AOAH, acyloxyacyl	CCAGCCTCTC[G/A]AATGGGCACA	S	G	A	S	S
				hydrolase
				(neutrophil)
G4417u5	WIAF-13842	HT0542	458	AOAH, acyloxyacyl	CAACTCGACG[G/A]TCCAGGCCTC	M	G	A	V	I
				hydrolase
				(neutrophil)
G4417u6	WIAF-13843	HT0542	1201	AOAH, acyloxyacyl	GATTTCTGGA[C/T]TCCACTGTTG	S	C	T	D	D
				hydrolase
				(neutrophil)
G4417u7	WIAF-13844	HT0542	1321	AOAH, acyloxyacyl	ACCTGAAGAA[A/G]TTTATAGAAA	S	A	G	K	K
				hydrolase
				(neutrophil)
G4417u8	WIAF-13845	HT0542	1404	AOAH, acyloxyacyl	GATGTCTCCA[G/A]TCGGAACAGT	M	G	A	S	N
				hydrolase
				(neutrophil)
G4417u9	WIAF-13846	HT0542	1759	AOAH, acyloxyacyl	AATTTACAAA[C/T]TTCAATCTTT	S	C	T	N	N
				hydrolase
				(neutrophil)
G4417u10	WIAF-13847	HT0542	1644	AOAH, acyloxyacyl	CTCCAGGTCA[G/A]CCCCTGCCAC	M	G	A	S	N
				hydrolase
				(neutrophil)
G442u1	WIAF-11828	M94582	933	IL8RA, interleukin	CACATCGACC[G/A]GGCTCTCGAT	M	G	A	R	Q
				8 receptor, alpha
G442u2	WIAF-11829	M94582	721	IL8RA, interleukin	TCATCGTGCC[A/G]CTGCTGATCA	S	A	G	P	P
				8 receptor, alpha
G442u3	WIAF-11780	M94582	1027	IL8RA, interleukin	GCCATGGACT[C/T]CTCAAGATTC	S	C	T	L	L
				8 receptor, alpha
G442u4	WIAF-11792	M94582	78	IL8RA, interleukin	ATGGACAGTC[A/C]CAGCTTTGAA	M	A	G	D	G
				8 receptor,
				alpha
G4423u1	WIAF-13752	HT2216	71	ADSL,	GCTATGCCAG[C/T]CCGGAGATGT	S	C	T	S	S
				adenylosuccinate
				lyase
G4423u2	WIAF-13794	HT2216	126	ADSL,	ATGGCGCCAG[C/T]TGTGGCTGTG	S	C	T	L	L
				adenylosuccinate
				lyase
G4423u3	WIAF-13795	HT2216	674	ADSL,	AGCTTGACAA[G/A]ATGGTCACAG	S	G	A	K	K
				adenylosuccinate
				lyase
G4428u1	WIAF-13954	HT97524	57	ADFP, adipose	TGGTCAACCT[C/A]CCCTTGGTGA	S	G	A	L	L
				differentiation
				related protein;
				adipophilin
G4434u1	WIAF-13506	HT0863	551	ARF3, ADP-	TCTGGAGACA[C/T]TACTTCCAGA	S	C	T	H	H
				ribosylation factor
				3
G444u1	WIAF-10172	U28694	398	CCR3, chemokine	CGACATCTTT[T/G]TCATAATCCT	M	T	G	F	V
				(C-C motif)
				receptor 3
G444u2	WIAF-10181	U28694	214	CCR3, chemokine	TCCTCATAAA[A/C]TACAGGAGGC	S	A	G	K	K
				(C-C motif)
				receptor 3
G4440u1	WIAF-14054	HT1392	136	ADRBK1, adrenergic,	GCAAGAAGAT[A/C]CTGCTGCCCG	S	A	G	I	I
				beta, receptor
				kinase 1
G445u1	WIAF-10183	U40373	319	Human cell	TAGAAGGCCA[C/T]CTGGTGATTC	S	C	T	H	H
				surface glyco-
				protein CD44 mRNA,
				complete cds.
G4456u1	WIAF-13629	HT0626	796	ALDOC, aldolase C,	CCCTGCTCAA[G/A]CCCAACATCC	S	G	A	K	K
				fructose-
				bisphosphate
G446u1	WIAF-11832	U64198	754	IL12RB2, inter-	TGAACCCTTC[C/G]CATGTAATTT	S	C	G	S	S
				leukin 12 receptor,
				beta 2
G446u2	WIAF-11795	U64198	2569	IL12RB2, inter-	TTTTCTCAAC[G/A]CATTACTTCC	S	G	A	T	T
				leukin 12 receptor,
				beta 2
G446u3	WIAF-11833	U64198	2500	IL12RB2, inter-	TGCAACGTAA[A/C]CCCAATTGCA	S	A	G	K	K
				leukin 12 receptor,
				beta 2
G446u4	WIAF-11835	U64198	1918	IL12RB2, inter-	CTCCTCGCCA[G/C]CTCTCTGCAA	M	G	C	Q	H
				leukin 12 receptor,
				beta 2
G446u5	WIAF-11793	U64198	991	IL12RB2, inter-	GTGGAGCAGA[C/A]ATCTTCGTTC	S	G	A	E	E
				leukin 12 receptor,
				beta 2
G446u6	WIAF-11794	U64198	2469	IL12RB2, inter-	AGTTCCCACC[G/C]AAATGAGAGG	M	G	C	G	A
				leukin 12 receptor,
				beta 2
G446a7	WIAF-13128	U64198	1964	IL12RB2, inter-	GGTGACTTGG[C/g]AGCCTCCCAG	M	C	g	Q	E
				leukin 12 receptor,
				beta 2
G446a8	WIAF-13129	U64198	2060	IL12RB2, inter-	TCTAAACTGG[C/G]TACCCACTCG	M	C	G	L	V
				leukin 12 receptor,
				beta 2
G447u1	WIAF-11796	X03663	384	CSF1R, colony	CCAGTGTCCC[C/T]GAGCTGGTCG	S	C	T	P	P
				stimulating factor
				1 receptor,
				formerly McDonough
				feline sarcoma
				viral (v-fms)
				oncogene homolog
G447u2	WIAF-11836	X03663	1026	CSF1R, colony	ACAACAACAC[T/C]AAGCTGCCAA	S	T	C	T	T
				stimulating factor
				1 receptor,
				formerly McDonough
				feline sarcoma
				viral (v-fms)
				oncogene homolog
G447u3	WIAF-11837	X03663	886	CSF1R, colony	CCTCAAAGTG[C/A]ACAAACTCAT	M	C	A	Q	K
				stimulating factor
				1 receptor,
				formerly McDonough
				feline sarcoma
				viral (v-fms)
				oncogene homolog
G447u4	WIAF-11797	X03663	2425	CSF1R, colony	GAAGAAATAT[G/A]TCCGCAGGGA	M	G	A	V	I
				stimulating factor
				1 receptor,
				formerly McDonough
				feline sarcoma
				viral (v-fms)
				oncogene homolog
G4473u1	WIAF-13904	HT1352	860	FUCA1,	TTCAAGCCAC[A/G]GAGCTTGCCA	M	A	G	Q	R
				fucosidase,
				alpha-L- 1,
				tissue
G4473u2	WIAF-13916	HT1352	440	FUCA1,	ACAAACTGGC[C/T]GAGTCCTGTG	M	C	T	P	L
				fucosidase,
				alpha-L- 1,
				tissue
G4479u1	WIAF-13637	HT1995	2465	AMPD2, adenosine	GCCTCAATGA[G/T]CCTGGTCCAT	—	G	T	—	—
				monophosphate
				deaminase 2
				(isoform L)
G4479u2	WIAF-13866	HT1995	1258	AMPD2, adenosine	TGGATGTGCA[T/C]GCGGACAGGA	S	T	C	H	H
				monophosphate
				deaminase 2
				(isoform L)
G4479u3	WIAF-13867	HT1995	1280	AMPD2, adenosine	CACTTTCCAT[C/T]CCTTTGACAA	M	C	T	R	C
				monophosphate
				deaminase 2
				(isoform L)
G4479u4	WIAF-13868	HT1995	1201	AMPD2, adenosine	TGCGGGAGGT[C/T]TTTGAGAGCA	S	C	T	V	V
				monophosphate
				deaminase 2
				(isoform L)
G4479u5	WIAF-13869	HT1995	1579	AMPD2, adenosine	GTACCAAGGG[C/T]CAGCTGGCCA	S	C	T	G	G
				monophosphate
				deaminase 2
				(isoform L)
G4492u1	WIAF-14084	HT3390	866	ANX11, annexin	CCTGGGGAGT[C/T]GCTCCAACAA	M	C	T	R	C
				XI (56 kD
				autoantigen)
G4492u2	WIAF-14085	HT3390	850	ANX11, annexin	AGGCCATCAT[T/C]GACTGCCTGG	S	T	C	I	I
				XI (56 kD
				autoantigen)
G450u1	WIAF-10170	X85740	1196	CCR4, chemokine	TCCAAATTTA[C/T]TCTGCTGACA	S	C	T	Y	Y
				(C-C motif)
				receptor 4
G4502u1	WIAF-13510	HT4840	165	ASS,	AAGCCTATGA[C/T]GTCATTGCCT	S	C	T	D	D
				argininosuccinate
				synthetase
G4502u2	WIAF-13511	HT4840	369	ASS,	GGCCCTGCAT[C/T]GCCCGCAAAC	S	C	T	I	I
				argininosuccinate
				synthetase
G4502u3	WIAF-13512	HT4840	73	ASS,	AATCCCAGAC[G/A]CTATGTCCAC	—	G	A	—	—
				argininosuccinate
				synthetase
G4502u4	WIAF-13513	HT4840	129	ASS,	TGGACACCTC[G/C]TGCATCCTCG	S	G	C	S	S
				argininosuccinate
				synthetase
G4502u5	WIAF-13514	HT4840	285	ASS,	AGTTTGTGGA[G/A]GAGTTCATCT	S	G	A	E	E
				argininosuccinate
				synthetase
G4502u6	WIAF-13515	HT4840	234	ASS,	AGGCACTGAA[C/A]CTTGGGGCCA	S	G	A	K	K
				argininosuccinate
				synthetase
G4502u7	WIAF-13516	HT4840	316	ASS,	CCAGTCCAGC[G/A]CACTGTATGA	N	G	A	A	T
				argininosuccinate
				synthetase
G4502u8	WIAF-13537	HT4840	426	ASS,	TGTCCCACGG[C/T]GCCACAGGAA	S	C	T	G	G
				argininosuccinate
				synthetase
G4502u9	WIAF-13538	HT4840	530	ASS,	GAATTCTACA[A/C]CCGGTTCAAG	M	A	G	N	S
				argininosuccinate
				synthetase
G4502u10	WIAF-13539	HT4840	750	ASS,	TTCTCGACAT[C/T]GAGTTCAAAA	S	C	T	I	I
				argininosuccinate
				synthetase
G4502u11	WIAF-13540	HT4840	960	ASS,	ATGCTCATTT[A/G]GACATCGAGG	S	A	G	L	L
				argininosuccinate
				synthetase
G4508u1	WIAF-13663	HT28557	1767	ARSD,	CAGTTTTCCA[T/C]GAGCAACATC	M	T	C	M	T
				arylsulfatase D
G4508u2	WIAF-13693	HT28557	433	ARSD,	TTCAGTGGAA[C/T]GCAGGCTCAG	S	C	T	N	N
				arylsulfatase D
G4508u3	WIAF-13694	HT28557	747	ARSD,	GGTTTCTTCT[C/G]TGTCTCCGCG	M	C	G	S	C
				arylsulfatase D
G4508u4	WIAF-13696	HT28557	1012	ARSD,	CCAGCACTGC[A/C]TTCCTGGGGA	S	A	G	A	A
				arylsulfatase D
G4508u5	WIAF-13697	HT28557	1302	ARSD,	CGAGTGATTG[G/A]AGAGCCCACG	M	G	A	G	E
				arylsulfatase D
G4508u6	WIAF-13698	HT28557	1285	ARSD,	GGGTGCTCCC[G/A]GCCCGCCGAG	S	G	A	P	P
				arylsulfatase D
G4508u7	WIAF-13699	HT28557	1807	ARSD,	AGCCGTGCTG[C/T]GGACATTTCC	S	C	T	C	C
				arylsulfatase D
G4508u8	WIAF-13718	HT28557	483	ARSD,	GCAAGAATCT[T/C]GCAGCAGCAT	M	T	C	L	S
				arylsulfatase D
G4518u1	WIAF-13809	HT3430	515	ASPA,	ACAACACCAC[C/T]TCTAACATGG	S	C	T	T	T
				aspartoacylase
				(aminoacylase 2,
				Canavan disease)
G4518u2	WIAF-13810	HT3430	851	ASPA,	AACTTCATTA[C/T]CCCCGGGATC	S	C	T	Y	Y
				aspartoacylase
				(aminoacylase 2,
				Canavan disease)
G4518u3	WIAF-13811	HT3430	787	ASPA,	CATCATTTCA[A/G]TGAAGGAAAA	M	A	G	N	S
				aspartoacylase
				(aminoacylase 2,
				Canavan disease)
G4518u4	WIAF-13837	HT3430	618	ASPA,	ACCCTGCTAC[G/A]TTTATCTGAT	M	G	A	V	I
				aspartoacylase
				(aminoacylase 2,
				Canavan disease)
G452a1	WIAF-10509	HT0695	553	APOA4,	ACCCAGGTCA[A/C]CACGCAGGCC	M	A	G	N	S
				apolipoprotein A-IV
G452a2	WIAF-13124	HT0695	563	APOA4,	ACACGCAGGC[C/T]GAGCAGCTGC	S	C	T	A	A
				apolipoprotein A-IV
G4524u1	WIAF-14120	HT1541	726	ATP5A1, ATP	CTCAATTGCT[A/G]TTGACACAAT	M	A	G	I	V
				synthase, H+
				transporting, mito-
				chondrial F1
				complex, alpha
				subunit, isoform 1,
				cardiac muscle
G4524u2	WIAF-14131	HT1541	153	ATP5A1, ATP	ATCTTTCATT[G/T]CTGCAAGGAA	M	G	T	A	S
				synthase, H+
				transporting, mito-
				chondrial F1
				complex, alpha
				subunit, isoform 1,
				cardiac muscle
G4526u1	WIAF-14130	HT4994	400	ATP5D, ATP	TCCATCGCAG[T/C]GAACGGCGAC	M	T	C	V	A
				synthase, H+
				transporting, mito-
				chondrial F1
				complex, delta
				subunit
G453u1	WIAF-10138	HT0768	1747	PDGFRB, platelet-	CTGCCGCCCA[C/T]GCTGCTGGGG	M	C	T	T	M
				derived growth
				factor receptor,
				beta polypeptide
G453u2	WIAF-10147	HT0768	2957	PDGFRB, platelet-	TTTTGCCTTT[A/G]AAGTGGATGG	S	A	G	L	L
				derived growth
				factor receptor,
				beta polypeptide
G453u3	WIAF-10148	HT0768	3608	PDGFRB, platelet-	AGCCGGAGCC[A/G]GAGCTGGAAC	S	A	G	P	P
				derived growth
				factor receptor,
				beta polypeptide
G453u4	WIAF-10149	HT0768	457	PDGFRB, platelet-	CAGGGCCTGG[T/G]CGTCACACCC	M	T	G	V	G
				derived growth
				factor receptor,
				beta polypeptide
G453u5	WIAF-10151	HT0768	1505	PDGFRB, platelet-	AGCTGACACT[G/C]GTTCGCGTGA	S	G	C	L	L
				derived growth
				factor receptor,
				beta polypeptide
G453u6	WIAF-10153	HT0768	3446	PDGFRB, platelet-	ACCCCAAACC[C/T]GAGCTTGCTG	S	C	T	P	P
				derived growth
				factor receptor,
				beta polypeptide
G453u7	WIAF-10161	HT0768	2030	PDGFRB, platelet-	TTTGGCAGAA[G/A]AAGCCACGTT	S	G	A	K	K
				derived growth
				factor receptor,
				beta polypeptide
G4533u1	WIAF-13616	HT1618	343	ATP synthase, H+	GTTACATGAT[C/T]GACAACGTGA	S	C	T	I	I
				transporting,
				subunit D,
				vacuolar
G4534u1	WIAF-13569	HT3556	654	ATP6E, ATPase, H+	TAAAGGTTTC[C/T]AACACCCTGG	S	C	T	S	S
				transporting,
				lysosomal
				(vacuolar
				proton pump) 31 kD
G4535u1	WIAF-13747	HT27972	357	ATP50, ATP	TCACTACCAA[C/T]CTGATCAATT	S	C	T	N	N
				synthase, H+
				transporting,
				mitochondrial F1
				complex, O subunit
				(oligomycin
				sensitivity
				conferring
				protein)
G4535u2	WIAF-13748	HT27972	144	ATP50, ATP	AGGTATACGG[T/C]ATTGAAGGTC	S	T	C	G	G
				synthase, H+
				transporting,
				mitochondrial F1
				complex, O subunit
				(oligomycin
				sensitivity
				conferring
				protein)
G4535u3	WIAF-13792	HT27972	329	ATP50, ATP	ATCACAGCAA[A/G]AGAGAGGTTC	M	A	G	K	R
				synthase, H+
				transporting,
				mitochondrial F1
				complex, O subunit
				(oligomycin
				sensitivity
				conferring
				protein)
G45439u1	WIAF-13711	HT48520	288	ATPase, 14 kDa	TGCCCTGGAC[G/A]CCCACCAGCA	M	G	A	A	T
				subunit, vacuolar
G4548u1	WIAF-14127	HT1574	3138	ATPase, Ca2+ trans-	CGCAATGTCT[T/C]TGACGGCATC	M	T	C	F	S
				porting membrane,
				isoform 2
G4548u2	WIAF-14137	HT1574	2089	ATPase, Ca2+ trans-	GCACTATCTG[C/T]GTGGCCTACC	S	C	T	C	C
				porting membrane,
				isoform 2
G4548u3	WIAF-14140	HT1574	2924	ATPase, Ca2+ trans-	CAGGACCATG[A/T]TGAAGAACAT	M	A	T	M	L
				porting membrane,
				isoform 2
G4549u1	WIAF-14161	HT1346	524	ATP2B4, ATPase,	TGCACTGACC[C/T]AGATTAATGT	N	C	T	Q	*
				Ca++ transporting,
				plasma membrane 4
G4549u2	WIAF-14162	HT1346	715	ATP2B4, ATPase,	ATGTCACGCT[C/T]ATCATCCTGC	S	C	T	L	L
				Ca++ transporting,
				plasma membrane 4
G4549u3	WIAF-14163	HT1346	508	ATP2B4, ATPase,	AGCTGCGTTC[G/A]ACGGATOCAC	S	G	A	S	S
				Ca++transporting,
				plasma membrane 4
G4549u4	WIAF-14166	HT1346	1084	ATP2B4, ATPase,	TGATCCAACG[G/A]AATGATCTCA	S	G	A	G	G
				Ca++ transporting,
				plasma membrane 4
G4552u1	WIAF-13630	HT0867	710	ATP7A, ATPase,	TACTAGCACT[A/G]TTGAAGGAAA	M	A	G	I	V
				Cu++ transporting,
				alpha polypeptide
				(Menkes syndrome)
G456u1	WIAF-100741	HT2834	408	EDN1, endothelin 1	CCTGGCGGCT[T/G]CGCCGGTCCA	S	T	G	L	L
G456u2	WIAF-10075	HT2834	585	EDN1, endothelin 1	CAGACCGTGA[A/G]AATAGATGCC	S	A	G	E	E
G456a3	WIAF-10507	HT2834	861	EDN1, endothelin 1	TGAAAGGCAA[T/G]CCCTCCAGAG	M	T	G	K	N
G4565u1	WIAF-14041	HT28561	320	ATP1G1, ATPase,	CGAGGCTGCT[G/A]TTACGGCTCA	S	G	A	L	L
				Na+/K+
				transporting, gamma
				1 polypeptide
G4565u2	WIAF-14062	HT28561	216	ATP1G1, ATPase,	CAGTGACGGG[G/A]ACAAAGGTCT	M	G	A	D	N
				Na+/K+
				transporting, gamma
				1 polypeptide
G4565u3	WIAF-14063	HT28561	315	ATP1G1, ATPase,	ACCGCCGAGG[C/A]TGCTGTTACG	M	C	A	L	M
				Na+/K+
				transporting, gamma
				1 polypeptide
G4565u4	WIAF-14064	HT28561	531	ATP1G1, ATPase,	TTTCCCCAGG[T/C]GAATGGGCTG	N	T	C	*	R
				Na+/K+
				transporting, gamma
				1 polypeptide
G4568u1	WIAF-14212	HT0082	717	AMFR, autocrine	TGCCTCATGC[A/G]TACGTCCCAC	M	A	G	I	V
				motility factor
				receptor
G457a1	WIAF-10489	HT2903	321	SELL, selectin L	ACAAATCTCT[C/T]ACTGAAGAAG	S	C	T	L	L
				(lymphocyte
				adhesion
				molecule 1)
G457a2	WIAF-10490	HT2903	577	SELL, selectin L	CCAGTGTCAG[T/C]TTGTGATTCA	M	T	C	F	L
				(lymphocyte
				adhesion
				molecule 1)
G457a3	WIAF-10491	HT2903	601	SELL, selectin L	TGAGCCTTTG[G/C]AGGCCCCAGA	M	G	C	E	Q
				(lymphocyte
				adhesion
				molecule 1)
G457a4	WIAF-10492	HT2903	637	SELL, selectin L	CTGTACTCAC[C/T]CTTTGGGAAA	M	C	T	P	S
				(lymphocyte
				adhesion
				molecule 1)
G4573u1	WIAF-13568	HT28320	943	NCAT2, mannosyl	CGGACAACCT[G/T]ACCCTGCGCT	S	G	T	L	L
				(alpha-1,6-)-
				glycoprotein beta-
				1,2-N-acetylgluco-
				saminyltransferase
G4574u1	WIAF-13805	HT0198	163	beta-1,4 N-	CGGCCTCCGG[C/G]TACCTCTTGC	M	C	G	L	V
				acetylgalacto-
				saminyltransferase
G4574u2	WIAF-13806	HT0198	415	beta-1,4 N-	TGCCACAAGA[G/A]AGCAGGAGTT	M	G	A	E	K
				acetylgalacto-
				saminyltransferase
G4574u3	WIAF-13807	HT0196	726	beta-1,4 N-	AACTACAACT[G/T]GTCACTTACA	S	G	T	L	L
				acetylgalacto-
				saminyltransferase
G4574u4	WIAF-13836	HT0198	559	beta-1,4 N-	AGGGCTGAGC[C/A]TTCAGGCAGC	M	C	A	L	I
				acetylgalacto-
				saminyltransferase
G4575u1	WIAF-13626	HT0341	1251	GCNT1, glucosaminyl	AGTATGATCT[A/G]TCTGACATGC	S	A	G	L	L
				(N-acetyl)
				transferase 1,
				core 2 (beta-1,6-N-
				acetylgluco-
				saminyltransferase)
G4577u1	WIAF-13971	HT1495	1268	SIAT1, sialyl-	ATTTCTTTAA[C/T]AACTACAAGA	S	C	T	N	N
				transferase 1
				(beta-galactoside
				alpha-2, 6-
				sialytransferase)
G458u1	WIAF-10063	HT2968	1464	ALB, albumin	GTGCAGAAGA[C/A]TATCTATCCG	M	C	A	D	E
G458u2	WIAF-10089	HT2968	1470	ALB, albumin	AAGACTATCT[A/C]TCCGTGGTCC	S	A	C	L	L
G458u3	WIAF-10091	HT2968	1707	ALB, albumin	TTGTTGAGCT[C/T]GTGAAACACA	S	C	T	L	L
G458a4	WIAF-10504	HT2968	889	ALB, albumin	CAGGGCGGAC[C/T]TTGCCAAGTA	M	C	T	L	F
G458a5	WIAF-10508	HT2968	1475	ALB, albumin	TATCTATCCG[T/A]GGTCCTGAAC	M	T	A	V	E
G458a6	WIAF-12091	HT2968	1330	ALB, albumin	CCAGAATGCG[C/T]TATTAGTTCG	S	C	T	L	L
G458a7	WIAF-12092	HT2968	1408	ALB, albumin	CCTAGGAAAA[G/a]TGGGCAGCAA	M	G	a	V	M
G4592u1	WIAF-14126	HT2128	985	branched-chain keto	ACCAGCCCTT[T/C]CTCATCGAGG	S	T	C	F	F
				acid dehydrogenase
				E1, alpha poly-
				peptide
G4593u1	WIAF-13574	HT97373	1743	BARD1, ERCA1	GCTAGCCACT[G/C]CTCAGTAATG	M	G	C	C	S
				associated RING
				domain 1
G4593u2	WIAF-13592	HT97373	1167	BARD1, ERCA1	TGTTCTTCAC[C/T]ACCTTCATGC	M	C	T	P	L
				associated RING
				domain 1
G4593u3	WIAF-13593	HT97373	1591	BARD1, ERCA1	AGAATGGGCA[C/TI GTGGATATAG	S	C	T	H	H
				associated RING
				domain 1
G4593u4	WIAF-13594	HT97373	2030	BARD1, ERCA1	AAAGTATGAA[A/G]TTCCTGAAGG	M	A	G	I	V
				associated RING
				domain 1
G4593u5	WIAF-13595	HT97373	2006	BARD1, ERCA1	AAGAAAAGTA[T/C]GTGAACAGGA	M	T	C	C	R
				associated RING
				domain 1
G4599u1	WIAF-13920	HT4273	1803	CDH13, cadherin 13,	TCGTACCCGA[C/T]GTCTCCTACG	S	C	T	D	D
				H-cadherin
(heart)
G4614u1	WIAF-13733	HT4835	91	S100A3, S100	AGGATGGCCA[G/A]GCCTCTGGAG	M	G	A	R	K
				calcium-binding
				protein A3
G4614u2	WIAF-13734	HT4835	203	S100A3, S100	TGCTGCAGAA[G/A]GAGCTGGCCA	S	G	A	K	K
				calcium-binding
				protein A3
G4614u3	WIAF-13769	HT4835	344	S100A3, S100	TCTACTGCCA[C/T]GAGTACTTCA	S	C	T	H	H
				calcium-binding
				protein A3
G462u1	WIAF-10134	HT4753	600	PDGFA, platelet-	ACGGGGTCCA[C/T]GCCACTAAGC	S	C	T	H	H
				derived growth
				factor alpha
				polypeptide
G4627u1	WIAF-14042	HT0771	186	ANX6, annexin VI	GGAGGCCATA[C/T]TGGACATAAT	S	C	T	L	L
				(p68)
G4627u2	WIAF-14043	HT0771	1664	ANX6, annexin VI	CAGACACACC[T/C]AGTGGAGACA	S	T	C	P	P
				(p68)
G4627u3	WIAF-14067	HT0771	1498	ANX6, annexin VI	AAGGAGCACT[A/G]TCACAAGTCC	M	A	G	Y	C
				(p68)
G4644u1	WIAF-13801	HT1736	1990	CPS1, carbamoyl-	TGGTGGAGAA[G/A]TCAGTGACAG	S	G	A	K	K
				phosphate
				synthetase 1,
				mitochondrial
G4644u2	WIAF-13802	HT1736	1866	CPS1, carbamoyl-	ATTGGCTACC[C/T]AGTGATGATC	M	C	T	P	L
				phosphate
				synthetase 1,
				mitochondrial
G4644u3	WIAF-13803	HT1736	1993	CPS1, carbamoyl-	TGGAGAAGTC[A/C]GTGACAGGTT	S	A	C	S	S
				phosphate
				synthetase 1,
				mitochondrial
G4644u4	WIAF-13804	HT1736	1860	CPS1, carbamoyl-	GACACCATTG[G/A]CTACCCAGTG	M	G	A	G	D
				phosphate
				synthetase 1,
				mitochondrial
G4644u5	WIAF-13831	HT1736	1087	CPS1, carbamoyl-	AGCCTGTTTT[C/T]AATATCACAA	M	G	T	L	F
				phosphate
				synthetase 1,
				mitochondrial
G4644u6	WIAF-13835	HT1736	1958	CPS1, carbamoyl-	CACAAAGGCC[T/C]TTGCTATGAC	M	T	C	F	L
				phosphate
				synthetase 1,
				mitochondrial
G4644u7	WIAF-13855	HT1736	1332	CPS1, carbamoyl-	AAAGCTACCA[C/A]CATTACATCA	M	C	A	T	N
				phosphate
				synthetase 1,
				mitochondrial
G4659u1	WIAF-14143	HT1183	1830	catenin, alpha	GTGCCAACGT[T/C]CCTCAACCGT	S	T	C	V	V
G466u1	WIAF-10164	U00968	2403	SREBF1, sterol	AGCAGTGCCC[C/A]CCAGGCCTGC	M	G	A	R	H
				regulatory element
				binding transcrip-
				tion factor 1
G4662u1	WIAF-13710	HT2142	2183	CTNNB1, catenin	TTTTGTTCCG[A/C]ATGTCTGAGG	S	A	C	R	R
				(cadherin
				associated
				protein), beta 1
				(88 kD)
G467a1	WIAF-13304	X72861	827	ADRB3, adrenergic,	GGCCATCGCC[T/C]GGACTCCGAG	M	T	C	W	R
				beta-3-,
				receptor
G467a2	WIAF-13305	X72861	832	ADRB3, adrenergic,	TCGCCTGGAC[T/A]CCGAGACTCC	S	T	A	T	T
				beta-3-,
				receptor
G467a3	WIAF-13306	X72861	870	ADRB3, adrenergic,	TTCGTCACTT[C/T]CCTGGCCGCA	M	C	T	S	L
				beta-3-,
				receptor
G467a4	WIAF-13307	X72861	1761	ADRB3, adrenergic,	TGCGCCGCCG[C/T]CCGCCCCGCC	M	C	T	A	V
				beta-3-,
				receptor
G467a5	WIAF-13305	X72861	1899	ADRB3, adrenergic,	TCTGTTGATC[A/C]GAACCTGTCG	—	A	C	—	—
				beta-3-,
				receptor
G4671u1	WIAF-13956	HT1925	161	NDUFB7, NADH	TGGTGGCCAC[A/C]CAGCAGGACA	S	A	G	T	T
				dehydrogenase
				(ubiquinone) 1
				beta subcomplex, 7
				(18 kD, B18)
G4673u1	WIAF-13889	HT0191	1349	CDC25A, cell	TCTCGGGCCA[G/C]CCCCAAAGAC	M	G	C	S	T
				division cycle 25A
G4674u1	WIAF-13821	HT1393	261	CDC25B, cell	ACCACCTCCC[C/T]GGGCTCGGCA	S	C	T	A	A
				division cycle 25B
G4674u2	WIAF-13822	HT1393	1297	CDC25B, cell	GATGGTCCCC[C/T]TATTCACGGG	S	C	T	L	L
				division cycle 25B
G4674u3	WIAF-13823	HT1393	1083	CDC25B, cell	ATAACCCCAG[C/A]CGGAGCCTGA	S	G	A	R	R
				division cycle 25B
G4674u4	WIAF-13827	HT1393	1446	CDC25B, cell	AGAGCCCCAT[C/T]CCCCCCTGTA	S	C	T	I	I
				division cycle 25B
G468a1	WIAF-13309	L37019	192	ASIP, agouti	AAATCCAAAC[C/A]CATCGGCACA	M	C	A	P	Q
				(mouse)-signaling
				protein
G4691u1	WIAF-13753	HT97602	179	CMKBR9, chemokine	TATAGCCTGA[T/A]TTTTGTGTTG	M	T	A	I	N
				(C-C motif)
				receptor 9
G4691u2	WIAF-13754	HT97602	134	CMKBR9, chemokine	AAGGATGCAG[T/C]GGTCTCCTTT	M	T	C	V	A
				(C-C motif)
				receptor 9
G4691u3	WIAF-13755	HT97602	193	CMKBR9, chemokine	TGTGTTGGGC[C/T]TCAGCGGGAA	M	C	T	L	F
				(C-C motif)
				receptor 9
G4691u4	WIAF-13756	HT97602	770	CMKBR9, chemokine	AAAATAGCTC[C/T]AGCCTTGGTG	M	C	T	A	V
				(C-C motif)
				receptor 9
G4691u5	WIAF-13759	HT97602	1130	CMKBR9, chemokine	TCTCAGAACT[A/C]CCCTAACAAG	M	A	C	Y	S
				(C-C motif)
				receptor 9
G4691u6	WIAF-13796	HT97602	482	CMKBR9, chemokine	AGGCTGAGGA[C/A]CCCGGCCAAG	M	C	A	T	N
				(C-C motif)
				receptor 9
G4691u7	WIAF-13797	HT97602	259	CMKBR9, chemokine	GATGGTTGAG[A/G]TCTATCTGCT	M	A	G	I	V
				(C-C motif)
				receptor 9
G4691u8	WIAF-13798	HT97602	434	CMKBR9, chemokine	ATGACCCTGG[A/G]CAAGTACCTG	M	A	G	D	G
				(C-C motif)
				receptor 9
G4691u9	WIAF-13799	HT97602	755	CMKBR9, chemokine	CAGGGCCGGG[C/T]TTTAAAAATA	M	C	T	A	V
				(C-C motif)
				receptor 9
G4699u1	WIAF-14040	HT4277	1426	BAAT, bile acid	TTCCAGATGT[C/T]ACCAGTCAAC	S	G	T	V	V
				Coenzyme A: amino
				acid N-acyl-
				transferase
				(glycine N-
				choloyltransferase)
G4726u1	WIAF-14128	HT48614	1606	AOC3, amine	TCCACCCCAG[T/C]GGGGCCATAG	S	T	C	S	S
				oxidase, copper
				containing 3
				(vascular adhesion
				protein 1)
G4726u2	WIAF-14129	HT48614	2242	AOC3, amine	TTCCTAACAC[A/G]GTGACTGTGG	S	A	G	T	T
				oxidase, copper
				containing 3
				(vascular adhesion.
				protein 1)
G4726u3	WIAF-14141	HT48614	659	AOC3, amine	CCTGCCCTAT[C/T]ACCGACGCCC	M	C	T	H	Y
				oxidase, copper
				containing 3
				(vascular adhesion
				protein 1)
G4744u1	WIAF-13683	HT2599	564	CTH, cystathionase	ATATTGTCCA[T/C]AAGCATGGAG	S	T	C	H	H
				(cystathionine
				gamma-lyase)
G4748u1	WIAF-14144	HT1061	242	CYBA, cytochrome	GGGACAGAAG[C/T]ACATGACCGC	M	C	T	H	Y
				b-245, alpha
				polypeptide
G4748u2	WIAF-14145	HT1061	265	CYBA, cytochrome	TGGTGAAGCT[G/C]TTCGGGCCCT	S	G	C	L	L
				b-245, alpha
				polypeptide
G4750u1	WIAF-14116	HT48417	156	CYB5, cytochrome	TGAAGTACTA[C/T]ACCCTAGAGG	S	C	T	Y	Y
				b-5
G4751u1	WIAF-13770	HT1285	495	UQCRC2, ubiquinol-	AGAATTTCGT[C/A]GTTGGGAAGT	M	C	A	R	S
				cytochrome c
				reductase core
				protein II
G4788u1	WIAF-13931	HT28249	1864	DSC3, desmocollin 3	CTGTTGATCC[T/C]GATGAACCTG	S	T	C	P	P
G4788u2	WIAF-13933	HT28249	2000	DSC3, desmocollin 3	TGGATTTCAA[G/T]AATATACCAT	N	G	T	E	*
G4788u3	WIAF-13945	HT28249	2524	DSC3, desmocollin 3	ACACTTACTC[G/A]GAGTGGCACA	S	G	A	S	S
G479u1	WIAF-12567	U36310	894	GPD2, glycerol-3-	GGGAAAGTCC[A/G]TGTGACCGGC	M	A	G	H	R
				phosphate
				dehydrogenase 2
				(mitochondrial)
G479u2	WIAF-12574	U36310	1657	GPD2, glycerol-3-	CTGGCAAAAG[G/T]TGGCCTATTG	M	G	T	R	S
				phosphate
				dehydrogenase 2
				(mitochondrial)
G479u3	WIAF-12575	U36310	1131	GPD2, glycerol-3-	GTTATTTTCT[T/C]CTTACCCTGG	M	T	C	F	S
				phosphate
				dehydrogenase 2
				(mitochondrial)
G480u1	WIAF-12175	HT336	250	GRB2, growth	AATGAAACCA[C/A]ATCCGTGGTT	M	C	A	H	N
				factor receptor-
				hound protein 2
G4819u1	WIAF-13985	HT97576	1804	EYA1, eyes absent	CCCTGCACCA[T/C]GCCTTGGAAC	S	T	C	H	H
				(Drosophila)
				homolog 1
G482u1	WIAF-12181	J04501	1186	GYS1, glycogen	CTGACGTCTT[T/C]CTGGAGGCAT	S	T	C	F	F
				synthase 1
				(muscle)
G482u2	WIAF-12195	J04501	1406	GYS1, glycogen	CCTTCCCGAC[A/G]TGAACAAGAT	M	A	G	M	V
				synthase 1
				(muscle)
G4827u1	WIAF-14177	HT97477	68	elongation	CGAGCTGGCC[A/G]TCATGGTCAT	M	A	G	H	R
G483a1	WIAF-12113	HT4341	1850	GSY2	TTACCAGCAT[C/T]CCAGACACCT	M	G	T	A	S
G483u2	WIAF-12148	HT4341	1130	GSY2	GTTTTTCATT[A/C]TCCCTGCCAA	M	A	C	M	L
G483u3	WIAF-12149	HT4341	880	GSY2	CCTTCAATGT[T/C]AAGAAATTTT	S	T	G	V	V
G483u4	WIAF-12150	HT4341	1115	GSY2	CATCACACTC[C/A]TGGTGTTTTT	M	G	A	V	M
G483u5	WIAF-12156	HT4341	1230	GSY2	GAAAACTTTG[C/A]AAAAAAACTC	M	G	A	G	E
G483u6	WIAF-12159	HT4341	2033	GSY2	TCACAGATAC[G/A]ATGACGAACA	M	G	A	D	N
G483u7	WIAF-12160	HT4341	1836	GSY2	TACTTACGCA[G/C]ATATTACCAC	M	G	C	R	T
G483u8	WIAF-12161	HT4341	1678	GSY2	CTTACGGTAT[T/C]TACATCGTTG	S	T	C	I	I
G483u9	WIAF-12177	HT4341	790	GSY2	GCGCTCACGT[G/C]TTCACCACGG	S	G	C	V	V
G483u10	WIAF-12188	HT4341	1728	GSY2	TCCAATCACC[T/C]GACTAAGTTT	M	T	C	L	P
G484u1	WIAF-12151	HT5111	487	GSY3	CATCAAAGTG[A/G]TTGGCAATGG	M	A	G	I	V
G484u2	WIAF-12187	HT5111	1141	GSY3	AACCCCGCAA[C/T]AAATCCCAGA	N	C	T	Q	*
G489u1	WIAF-12152	HT2607	1181	IRS1, insulin	AAGAAGTGGC[G/A]GCACAAGTCG	M	G	A	R	Q
				receptor
				substrate 1
G489u2	WIAF-12184	HT2607	1031	IRS1, insulin	ATGGCCAGCC[C/T]TCCGGAGAGC	M	C	T	P	L
				receptor
				substrate 1
G492a1	WIAF-13345	L08603	307	MC4R, melanocortin	AGAAACCATT[A/C]TCATCACCCT	M	A	G	I	V
				4 receptor
G493u1	WIAF-12154	X67594	346	MC1R, melanocortin	CGCGCTGGTG[G/T]TGGCCACCAT	M	G	T	V	L
				1 receptor
				(alpha melanocyte
				stimulating
				hormone receptor)
G493u2	WIAF-12167	X67594	646	MC1R, melanocortin	GACCCTGCCG[C/T]GGGCGCGGCA	M	C	T	R	W
				1 receptor
				(alpha melanocyte
				stimulating
				hormone receptor)
G493u3	WIAF-12170	X67594	1110	MC1R, melanocortin	AGGTCCTGAC[A/G]TGCTCCTGGT	S	A	G	T	T
				1 receptor
				(alpha melanocyte
				stimulating
				hormone receptor)
G493u4	WIAF-12186	X67594	442	MC1R, melanocortin	CGGGAGCAAC[C/T]TGCTCGAGAC	M	G	T	V	L
				1 receptor
				(alpha melanocyte
				stimulating
				hormone receptor)
G498u1	WIAF-11809	J04127	1305	CYP19, cytochrome	CTTATAGGTA[C/T]TTTCAGCCAT	S	C	T	Y	Y
				P450, subfamily
				XIX (aromatization
				of androgens)
G498u2	WIAF-11810	J04127	1377	CYP19, cytochrome	TGAAAGCCAT[C/T]CTCGTTACAC	S	C	T	I	I
				P450, subfamily
				XIX (aromatization
				of androgens)
G498u3	WIAF-11811	J04127	1406	CYP19, cytochrome	CGATTCCACG[T/C]GAAGACATTG	M	T	C	V	A
				P450, subfamily
				XIX (aromatization
				of androgens)
G498u4	WIAF-11838	J04127	1055	CYP19, cytochrome	ATTGCTGACA[G/A]AGACATAAAG	M	G	A	R	K
				P450, subfamily
				XIX (aromatization
				of androgens)
G498u5	WIAF-11800	J04127	1001	CYP19, cytochrome	ATTGCAAAGC[A/C]CCCTAATGTT	M	A	G	H	R
				P450, subfamily
				XIX (aromatization
				of androgens)
G499u1	WIAF-11785	HT1439	2142	ESR1, estrogen	TCCCTGCCAC[A/G]GTCTGAGAGC	S	A	G	T	T
				receptor 1
G499u2	WIAF-11801	HT1439	443	ESR1, estrogen	CCCCTGAACC[G/A]TCCGCAGCTC	M	G	A	R	H
				receptor 1
G500u1	WIAF-11803	X99101	793	ESR1, estrogen	CATGATCAGC]T/C]GGGCCAAGAA	M	T	C	W	R
				receptor 1
G500u2	WIAF-11816	X99101	489	ESR1, estrogen	GGAAGTGTTA[C/T]GAAGTGGGAA	S	C	T	Y	Y
				receptor 1
G500u3	WIAF-11817	X99101	474	ESR1, estrogen	AGGCCTGCCG[A/G]CTTCGGAAGT	S	A	G	R	R
				receptor 1
G505u1	WIAF-11824	HT1113	1063	PRLR, prolactin	GCTTTCAAGC[C/A]CTATAGCATC	M	G	A	G	D
				receptor
G505u2	WIAF-11827	HT1113	2083	PRLR, prolactin	GCAACATCAA[C/A]CAAGTCCAGG	M	G	A	S	N
				receptor
G505u3	WIAF-11787	HT1113	582	PRLR, prolactin	GAGGACATAC[A/G]TCATGATGGT	M	A	G	I	V
				receptor
G505u4	WIAF-11802	HT1113	792	PRLR, prolactin	CCTGTATGAA[A/C]TTCGATTAAA	M	A	C	I	L
				receptor
G509u1	WIAF-11789	M32313	378	SRD5A1, steroid-S-	CACTGTTCGC[A/G]TGTACAATGG	S	A	G	A	A
				alpha-reductase,
				alpha polypeptide 1
				(3-oxo-5 alpha-
				steroid delta 4-
				dehydrogenase
				alpha 1)
G510a1	WIAF-13348	U17280	582	STAR, steroidogenic	CCAATGTCAA[C/A]GAGATCAAGG	S	G	A	K	K
				acute regulatory
				protein
G52u1	WIAF-10224	HT0488	1139	inhibin, beta B	CCAACATGAT[T/C]GTGGAGGAGT	S	T	C	I	I
G520u1	WIAF-13507	D31770	517	ACVR2, activin A	CTTATTTTCC[G/A]GAGATGGAAG	S	G	A	P	P
				receptor, type
				II
G520u2	WIAF-13532	D31770	1177	ACVR2, activin A	CAGCTTGCAT[T/G]GCTGACTTTG	M	T	G	I	M
				receptor, type
				II
G520u3	WIAF-13533	D31770	1189	ACVR2, activin A	CTGACTTTGG[G/C]TTGGCCTTAA	S	G	C	G	G
				receptor, type
				II
G520u4	WIAF-13534	D31770	1024	ACVR2, activin A	TCTCTTCGAA[T/C]GAACTGTGTC	S	T	C	N	N
				receptor, type
				II
G523u1	WIAF-12155	HT4996	538	OXTR, oxytocin	TGACGGGGAA[C/T]GCGTGTGTGC	S	C	T	N	N
				receptor
G523u2	WIAF-12180	HT4996	1057	OXTR, oxytocin	TCTGGCAGAA[C/T]TTGCGGCTCA	S	C	T	N	N
				receptor
G524a1	WIAF-13349	L05144	190	PCK1, phosphoenol-	TGGACAGCCT[G/A]CCCCAGGCAG	S	G	A	L	L
				pyruvate carboxy-
				kinase 1 (soluble)
G528u1	WIAF-11831	V00572	988	PGK1, phospho-	AAGCCACTGT[G/C]GCTTCTGGCA	S	G	C	V	V
				glycerate kinase 1
G53u1	WIAF-10307	HT0508	723	DNA repair protein	CCAGCGACCC[G/A]GCAGGACCTA	S	G	A	P	P
				XRCC1
G53u2	WIAF-10308	HT0508	746	DNA repair protein	TATGCAGCTG[C/T[TACCCTCCAG	M	C	T	A	V
				XRCC1
G53u3	WIAF-10309	HT0508	1884	DNA repair protein	GGGATCCCAG[C/T]TTTGAGGAGG	S	C	T	S	S
				XRCC1
G53u4	WIAF-10362	HT0508	425	DNA repair protein	AACCCCAACC[G/A]CGTTCGCATG	M	G	A	R	H
				XRCC1
G534a1	WIAF-13311	U28281	1284	SCTR, secretin	GCTTCCTCAA[T/C]GGGGAGGTGC	S	T	C	N	N
				receptor
G534a2	WIAF-13311	U28281	1404	SCTR, secretin	AGCACAGCCA[G/A]GGCACCTGCA	S	G	A	Q	Q
				receptor
G535u1	WIAF-12157	HT5001	1158	SHC1	ATGCTCTTCG[G/C]GTGCCTCCAC	S	G	C	R	R
G535u2	WIAF-12196	HT5001	774	SHC1	ATGAGGAGGA[G/A]GAAGAGCCAC	S	G	A	E	E
G536u1	WIAF-13923	M20747	535	SLC2A4, solute	GCCTGCCCAA[C/T]GCTGCTGCCT	S	C	T	N	N
				carrier family 2
				(facilitated
				glucose
				transporter),
				member 4
G538u1	WIAF-11812	M55531	438	SLC2A5, solute	GCAGCAGAGT[C/T]GCCACATCAT	S	C	T	V	V
				carrier family 2
				(facilitated
				glucose
				transporter),
				member 5
G538u2	WIAF-11813	M55531	124	SLC2A5, solute	GACGCTTGTG[C/T]TTGCCCTGGC	M	C	T	L	F
				carrier family 2
				(facilitated
				glucose
				transporter)
				member 5
G538u3	WIAF-11791	M55531	816	SLC2A5, solute	ACAGGGAGGT[C/A]GCCGAGATCC	S	G	A	V	V
				carrier family 2
				(facilitated
				glucose
				transporter),
				member 5
G539u1	WIAF-12158	K03195	224	Human (HepG2) glu-	TCATGCTGCC[T/C]GTCCGAGGAC	S	T	C	A	A
				cose transporter
				gene mRNA,
				complete cds.
G539u2	WIAF-12191	K03195	1244	Human (HepG2) glu-	CCATCGCGCT[A/C]CCACTCCTGG	S	A	G	L	L
				cose transporter
				gene mRNA,
				complete cds.
G540a1	WIAF-12114	HT960	1100	SOS1	AGTGAAGATC[A/C]ACAACACAAG	M	A	C	Q	P
G540u2	WIAF-12165	HT950	933	SOS1	ATGATCGTTT[C/T]CTTAGTCAGT	S	C	T	F	F
G540u3	WIAF-12178	HT960	399	SOS1	TACTACCAGT[C/T]TTACAATACA	S	C	T	V	V
G540u4	WIAF-12193	HT960	195	SOS1	CTCAGCCCCG[A/C]AGTCCTTCAG	S	A	C	R	R
G540u5	WIAF-12197	HT960	1329	SOS1	GTTGTAATCA[A/C]TTTATAATCC	S	A	G	E	E
G540u6	WIAF-12198	HT960	1339	SOS1	ATTTATAATC[C/A]AACCAACTCT	M	G	A	E	K
G543a1	WIAF-13312	J00306	1373	SST, somatostatin	AACCAGGAAC[T/C]CCCCAACTAC	M	T	C	L	P
G543a2	WIAF-13313	J00306	1603	SST, somatostatin	ACTATTGTCC[A/G]TATCACACCT	—	A	G	—	—
G544u1	WIAF-12174	HT27489	982	SUR, sulfonylurea	CCATTGACAT[G/C]GCCACGGAAA	M	G	C	M	I
				receptor
				(hyperinsulinemia)
G546u1	WIAF-13618	HT225	426	TKT, transketolase	GCTACATTGC[C/T]CAGCAGAACA	S	C	T	A	A
				(Wernicke Korsakoff
				syndrome)
G551u1	WIAF-11709	HT1118	257	TNFRSF1B, tumor	GCTGCAGCAA[A/G]TGCTCGCCGG	S	A	G	K	K
				necrosis factor
				receptor super-
				family, member 1B
G551u2	WIAF-11710	HT1118	449	TNFRSF1B, tumor	TCTGCACCTG[C/T]AGGCCCGGCT	S	C	T	C	C
				necrosis factor
				receptor super-
				family, member 1B
G551u3	WIAF-11719	HT1118	648	TNFRSF1B, tumor	GATCTGTAAC[G/A]TGGTGGCCAT	M	G	A	V	M
				necrosis factor
				receptor super-
				family, member 1B
G551u4	WIAF-11673	HT1118	676	TNFRSF1B, tumor	AATGCAACCA[T/C]CCATGCAGTC	M	T	G	M	R
				necrosis factor
				receptor super-
				family, member 1B
G551u5	WIAF-11720	HT1118	808	TNFRSF1B, tumor	CCAAGCACCT[C/T]CTTCCTGCTC	M	C	T	S	F
				necrosis factor
				receptor super-
				family, member 1B
G552u1	WIAF-12229	HT5108	384	TRAP3	GCCGCTGCCC[G/AICTCATGCTGA	S	G	A	P	P
G555u1	WIAF-12211	U94592	478	UCP2, uncoupling	CGCGCTACAG[T/C]CAGCGCCCAG	M	T	C	V	A
				protein 2
				(mitochondrial,
				proton carrier)
G556u1	WIAF-11804	AF001787	480	UCP2, uncoupling	TCGGCCTCTA[T/C]GACTCCCTCA	S	T	C	Y	Y
				protein 2
				(mitochondrial,
				proton carrier)
G556u2	WIAF-11805	AF001787	563	UCP2, uncoupling	TGCACCACAG[G/A]AGCCATGGCG	M	G	A	G	E
				protein 2
				(mitochondrial,
				proton carrier)
G556u3	WIAF-11823	AF001787	1113	UCP2, uncoupling	TACGCCAATC[A/C]CCCTTTTGAA	S	A	G	S	S
				protein 2
				(mitochondrial,
				proton carrier)
G556u4	WIAF-11782	AF001787	386	UCP2, uncoupling	ATCCTGACCA[T/C]GGTGCGGACT	M	T	C	M	T
				protein 2
				(mitochondrial,
				proton carrier)
G561a1	WIAF-12111	HT1176	2430	IDE, insulin-	ACTCTGGCAT[C/A]GAGATATACT	S	C	A	I	I
				degrading enzyme
G561u2	WIAF-12222	HT1176	3099	IDE, insulin-	ATATTAACTT[C/G]ATGGCTGCAA	M	C	G	F	L
				degrading enzyme
GSG2u1	WIAF-12223	HT27503	680	tumor necrosis	CCTGTAGTGA[A/C]TCGGCCGCTG	M	A	C	N	T
				factor receptor
				type 1 associated
				protein
G562u2	WIAF-12224	HT27503	900	tumor necrosis	CGCTCCAGCG[C/A]CTGGTGGAGG	S	C	A	R	R
				factor receptor
				type 1 associated
				protein
G573u1	WIAF-12199	HT28094	469	SSTR1, somatostatin	GGACCGCTAC[G/C]TGGCCGTGGT	M	G	C	V	L
				receptor 1
G573u2	WIAF-12208	HT28094	480	SSTR1, somatostatin	TGGCCCTGGT[G/A]CATCCCATCA	S	G	A	V	V
				receptor 1
G573u3	WIAF-12209	HT28094	879	SSTR1, somatostatin	TGCAGCTGGT[T/C]AACGTGTTTG	S	T	C	V	V
				receptor 1
G574u1	WIAF-11822	HT4058	1054	SSTR5, somatostatin	GCCACGGAGC[C/T]GCGTCCAGAC	M	C	T	P	L
				receptor 5
G575u1	WIAF-12200	HT28095	99	SSTR3, somatostatin	ACGTGTCGGC[C/A]GGCCCAAGCC	S	G	A	A	A
				receptor 3
G575u2	WIAF-12217	HT28095	453	SSTR3, somatostatin	CCACCCGGTC[G/A]GCCCGCTGGC	S	G	A	S	S
				receptor 3
G585u1	WIAF-12204	HT1022	1133	PYGL,	AGCTGAATGA[T/C]ACTCACCCTC	S	T	C	D	D
				phosphorylase,
				glycogen;
				liver (Hers
				disease, glycogen
				storage disease
				type VI)
G585u2	WIAF-12205	HT1022	1988	PYGL,	AGCTGATCAC[T/C[TCAGTGGCAG	S	T	C	T	T
				phosphorylase,
				glycogen;
				liver (Hers
				disease, glycogen
				storage disease
				type VI)
G585u3	WIAF-12225	HT1022	1883	PYGL,	TGTACAACCC[C/T]ATTAAGAAAG	S	C	T	R	R
				phosphorylase,
				glycogen;
				liver (Hers
				disease, glycogen
				storage disease
				type VI)
G585u4	WIAF-12226	HT1022	2037	PYGL,	AAGCAAGTTG[A/G]AAGTCATCTT	M	A	G	K	E
				phosphorylase,
				glycogen;
				liver (Hers
				disease, glycogen
				storage disease
				type VI)
G585u5	WIAF-12231	HT1022	1387	PYGL,	GATGTGGACC[C/G]TCTGAGAAGG	M	C	G	P	R
				phosphorylase,
				glycogen;
				liver (Hers
				disease, glycogen
				storage disease
				type VI)
G586a1	WIAF-12112	HT1878	2410	PFKM,	CCGGGGAAGC[T/G]GCCGTCTAAA	S	T	G	A	A
				phosphofructo-
				kinase, muscle
G586u2	WIAF-12206	HT1878	375	PFKM,	GGACCACTCC[G/A]AGCTCCCTAC	M	G	A	R	Q
				phosphofructo-
				kinase, muscle
G586u3	WIAF-12207	HT1878	322	PFKM,	TGCGAGGCAC[C/A]GTGATTGGAA	S	G	A	T	T
				phosphofructo-
				kinase, muscle
G586u4	WIAF-12227	HT1878	334	PFKM,	TGATTGGAAG[T/C]GCCCGGTGCA	S	T	C	S	S
				phosphofructo-
				kinase, muscle
G586u5	WIAF-12228	HT1878	408	PFKM,	CGTCGGATCA[C/G]CAATCTCTGT	M	C	G	T	S
				phosphofructo-
				kinase, muscle
G586u6	WIAF-12235	HT1878	717	PFKM,	CACTGTGGAT[A/G]CCTGGCCCTT	M	A	G	Y	C
				phosphofructo-
				kinase, muscle
G587u1	WIAF-12615	HT3847	366	phosphofructo-	ATGCCAGCCT[T/C]ACAGGTGCCA	S	T	C	L	L
				kinase, liver
G589u1	WIAF-12210	L39211	1327	CPT1A, carnitine	CAGCGTTCTT[C/T]GTGACGTTAG	S	C	T	F	F
				palmitoyl-
				transferase I,
				liver
G589u2	WIAF-12215	L39211	2080	CPT1A, carnitine	AATATCTCGC[T/C]GTGGAGTCCC	S	T	C	A	A
				palmitoyl-
				transferase I,
				liver
G589u3	WIAF-12216	L39211	679	CPT1A, carnitine	ACTTCAAACG[C/T]ATGACAGCAC	S	G	T	R	R
				palmitoyl-
				transferase I,
				liver
G589u4	WIAF-12218	L39211	1844	CPT1A, carnitine	CCTCACATAC[G/C]AGGCCTCCAT	M	G	C	E	Q
				palmitoyl-
				transferase I,
				liver
G592u1	WIAF-11814	X96586	1089	NSMAF, neutral	TCCGGGATCT[C/T]AGTAAGCCAG	S	C	T	L	L
				sphingomyelinase
				(N-SMase)
				activation
				associated
				factor
G592u2	WIAF-11815	X96586	2020	NSMAF, neutral	AAGTATATCA[T/G]TTTCAAATAT	M	T	G	F	V
				sphingomyelinase
				(N-SMase)
				activation
				associated
				factor
G592u3	WIAF-11834	X96586	1673	NSMAF, neutral	GTAGCCATGC[T/C]TACGCAAATC	M	T	C	L	P
				sphingomyelinase
				(N-SMase)
				activation
				associated
				factor
G592u4	WIAF-11784	X96586	1889	NSMAF, neutral	CACGAGCACT[A/G]TAAAATCCAC	M	A	C	Y	C
				sphingomyelinase
				(N-SMase)
				activation
				associated
				factor
G592u5	WIAF-11798	X96586	1677	NSMAF, neutral	CCATGCTTAC[G/A]CAAATCTTGG	S	G	A	T	T
				sphingomyelinase
				(N-SMase)
				activation
				associated
				factor
G592u6	WIAF-11799	X96586	2429	NSMAF, neutral	TGCCATTCAG[G/C]GATTCTATGT	M	G	C	G	A
				sphingomyelinase
				(N-SMase)
				activation
				associated
				factor
G592a7	WIAF-13156	X96586	2205	NSMAF, neutral	ATTCTGCATC[G/A]TGGGACTCTA	S	G	A	S	S
				sphingomyelinase
				(N-SMase)
				activation
				associated
				factor
GS94u1	WIAF-10065	HT3921	1153	annexin V, alt.	TTGTGAAATC[T/A]ATTCGAAGTA	S	T	A	S	S
				transcript 2
G594u2	WIAF-10098	HT3921	567	annexin V, alt.	CGAAGTAATG[C/T]TCACCGCCAG	M	C	T	A	V
				transcript 2
G594u3	WIAF-10099	HT3921	774	annexin V, alt.	ATTGCTTCAA[G/C]CACACCTCAA	M	G	C	R	T
				transcript 2
G594a4	WIAF-10505	HT3921	424	annexin V, alt.	GAGTAGTCGC[C/T]ATGCCACACG	—	C	T	—	—
				transcript 2
G594a5	WIAF-13123	HT3921	571	annexin V, alt.	GTAATGCTCA[G/C]CGCCAGGAAA	M	G	C	Q	H
				transcript 2
G595u1	WIAF-12203	HT27983	1008	NRIP1, nuclear	TGCAACATTA[C/T]AGGCTGTTGC	N	C	T	Q	*
				receptor
				interacting
				protein 1
G595u2	WIAF-12220	HT27983	785	NRIP1, nuclear	CCCTCAGTCA[T/C]GATTCTTTAA	S	T	C	H	H
				receptor
				interacting
				protein 1
G595u3	WIAF-12232	HT27983	1231	NRP1, nuclear	GTTGGCAGTT[A/T]CCAGCTCCCA	M	A	T	Y	F
				receptor
				interacting
				protein 1
G595u4	WIAF-12261	HT27983	2048	NRIP1, nuclear	GCAGTACTCA[G/A]TCTCAAAACC	S	G	A	Q	Q
				receptor
				interacting
				protein 1
C595u5	WIAF-12274	HT27983	2376	NRIP1, nuclear	TCCTCAACCA[G/T]GGCTTTCTGG	M	G	T	G	W
				receptor
				interacting
				protein 1
G595u6	WIAF-12275	HT27983	3498	NRIP1, nuclear	ACTATATTAC[A/G]TGCTTCAAAA	M	A	G	M	V
				receptor
				interacting
				protein 1
G595u7	WIAF-12276	HT27983	3671	NRIP1, nuclear	ACAATAGCCA[T/C]ATGGGAAATA	S	T	C	H	H
				receptor
				interacting
				protein 1
G595u8	WIAF-12294	HT27983	2020	NRIP1, nuclear	ATCAAATGGA[A/G]TTCCCCACCA	M	A	G	N	S
				receptor
				interacting
				protein 1
G595u9	WIAF-12295	HT27983	3140	NRIP1, nuclear	ATTTGTCCCC[G/A]CACAGAAGTA	S	G	A	P	P
				receptor
				interacting
				protein 1
G596u1	WIAF-10144	HT3537	3299	PC, pyruvate	TGCGGTCCAT[C/T]TTGGTCAAGG	S	C	T	I	I
				carboxylase
G596u2	WIAF-10158	HT3537	2662	PC, pyruvate	ACCAACCTCC[A/C]CTTCCAGGCC	M	A	C	H	P
				carboxylase
G596u3	WIAF-10159	HT3537	2156	PC, pyruvate	CCATCTCATA[C/A]ACGGGCGACG	N	C	A	Y	*
				carboxylase
G598a1	WIAF-12118	HT48666	5585	HERC1, hect	GGGACCTATG[C/T]TGATAAACTG	M	C	T	A	V
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u2	WIAF-12236	HT48666	4456	HERC1, hect	CCTGTTAATA[T/C]TAGGAGTAAG	S	T	C	L	L
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u3	WIAF-12237	HT48665	6356	HERC1, hect	GGTAATGAAG[G/T]CACGTGTGTT	M	G	T	G	V
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u4	WIAF-12240	HT48666	12219	HERC1, hect	GTACCTTTGT[C/T]ATCCAGGCCA	S	C	T	V	V
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u5	WIAF-12241	HT48666	12480	HERC1, hect	CCAGGCAGAT[C/G]GAGGCCTTAC	M	C	G	I	M
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u6	WIAF-12244	HT48666	12975	HERC1, hect	GAGTAATCAT[T/A]GAAGATGTGG	S	T	A	I	I
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u7	WIAF-12245	HT48666	1424	HERC1, hect	TCCAATAATC[A/T]GTCAACTTTA	M	A	T	Q	L
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u8	WIAF-12250	HT48666	5854	HERC1, hect	TTCAAAAGCA[A/T]TTCAATCAAA	M	A	T	I	F
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u9	WIAF-12251	HT48666	6754	HERC1, hect	TATTCAGCTC[G/A]TCCGTATCCT	M	G	A	V	I
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u10	WIAF-12252	HT48666	7535	HERC1, hect	ATCTTTACCT[C/T]GGTCCTATGA	S	C	T	L	L
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u11	WIAF-12254	HT48666	9189	HERC1, hect	GTGGAAATCC[A/G]TACTACCTGT	S	A	G	P	P
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u12	WIAF-12255	HT48666	10119	HERC1, hect	TTGTGGCATT[G/C]CTAGCAGACA	M	G	C	L	F
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u13	WIAF-12257	HT48666	11109	HERC1, hect	ATCCATCTAT[T/C]GTAAATGGCA	S	T	C	I	I
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u14	WIAF-12258	HT48666	13513	HERC1, hect	CTATGGACCT[C/T]AGATAACTGT	N	C	T	Q	*
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G5958u15	WIAF-12259	HT48666	13697	HERC1, hect	ACCATCACAG[A/C]GATGTGCCAG	M	A	G	E	G
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u16	WIAF-12255	HT48666	1098	HERC1, hect	CCCTTTACGA[G/A]GCAGCATTAT	S	G	A	E	E
				(homologous to the
				E6 AP (UDE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u17	WIAF-12272	HT48666	6079	HERC1, hect	TATGTGGGAG[A/G]CACCCATTGC	M	A	G	T	A
				(homologous to the
				E6 AP (UHE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u18	WIAF-12273	HT48666	9551	HERC1, hect	AAGAGCTCCT[C/T]TGGGAGAATA	M	C	T	S	F
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u19	WIAF-12277	HT48666	666	HERC1, hect	GTCTTTGCAA[C/T]GATGTCATTC	S	C	T	N	N
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u20	WIAF-12278	HT48666	882	HERC1, hect	GCTCATTGCG[A/G]TATCTTCTTG	S	A	G	R	R
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u21	WIAF-12279	HT48666	893	HERC1, hect	TATCTTCTTC[A/T]ATGGATAGAA	M	A	T	E	V
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u22	WIAF-12280	HT48666	13276	HERC1, hect	AGAACTCAGC[A/C]TTCACACGGT	M	A	G	I	V
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u23	WIAF-12283	HT48666	6519	HERC1, hect	CCTGTCTGTT[A/T]GACATGGAAC	M	A	T	L	F
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u24	WIAF-12284	HT48666	8386	HERC1, hect	GGGGTTCTCT[C/T]TTCGGCAGAT	M	C	T	L	F
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u25	WIAF-12286	HT48666	10266	HERC1, hect	CAGCTCAGCA[A/T]CTCGTGCGCA	M	A	T	Q	H
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u26	WIAF-12287	HT48666	10099	HERC1, hect	CTTTGTTGTA[A/G]CACAGGCCCT	M	A	G	T	A
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u27	WIAF-12289	HT48666	11835	HERC1, hect	AGAACTGTCT[G/C]CCTGACCCTG	S	G	C	L	L
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u28	WIAF-12290	HT48666	12689	HERC1, hect	TTAAACCACA[C/T]TTTGGCAGTG	M	C	T	T	I
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u29	WIAF-12291	HT48666	14655	HERC1, hect	ACGTGGACAA[C/T]GCCGAGGGCT	S	C	T	N	N
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u30	WIAF-12296	HT48666	393	HERC1, hect	ATTCCCCATT[T/C]GCCGGGGCAC	S	T	C	F	F
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u31	WIAF-12297	HT48666	479	HERC1, hect	GGCAAGGTGA[A/G]GCAGCAGCAG	M	A	G	K	R
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u32	WIAF-12298	HT48666	1197	HERC1, hect	ATGCTCCCAT[T/C]GTCTCCGAAA	S	T	C	I	I
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u33	WIAF-12300	HT48666	3595	HERC1, hect	TCCAGAGGAA[C/T]AGCACACTGC	N	C	T	Q	*
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G598u34	WIAF-12301	HT48666	3661	HERC1, hect	CACTCCTCAA[T/C]TGGATAAATG	S	T	C	L	L
				(homologous to the
				E6 AP (UBE3A)
				carboxyl terminus)
				domain and RCC1
				(CHC1)-like domain
				(RLD) 1
G601u1	WIAF-12246	HT27734	106	PRKMK5, protein	TGGAGAACCA[G/A]GTGCTGGTAA	S	G	A	Q	Q
				kinase, mitogen-
				activated, kinase 5
				(MAP kinase
				kinase 5)
G601u2	WIAF-12247	HT27734	351	PRKMK5, protein	GTAAATGGAC[A/G]GTTAATAGAG	M	A	G	Q	R
				kinase, mitogen-
				activated, kinase 5
				(MAP kinase
				kinase 5)
G601u3	WIAF-12292	HT27734	617	PRKMK5, protein	AGCATATCAT[G/C]TCCCGAGTGG	M	G	C	V	L
				kinase, mitogen-
				activated, kinase 5
				(MAP kinase
				kinase 5)
G603u1	WIAF-12248	HT4291	1336	mitogen-activated	AGTCATCAGC[T/C]TTGTGCCACC	M	T	C	F	L
				protein (MAP)
				kinase p38
G603u2	WIAF-12281	HT4291	1230	mitogen-activated	CTCAGTACCA[C/T]GATCCTGATG	S	C	T	H	H
				protein (MAP)
				kinase p38
G610u1	WIAF-12249	HT48690	1012	protein kinase,	CCGAGCCATA[T/C]GATGAGAGCG	S	T	C	V	Y
				mitogen-activated,
				p38Beta (MAP kinase
				p38Beta)
G610u2	WIAF-12263	HT48690	799	protein kinase,	AAATCTCCTC[G/A]GAACACGCCC	S	G	A	S	S
				mitogem-activated,
				p38Beta (MAP kinase
				p38Beta)
GS10u3	WIAF-12264	HT48690	848	protein kinase,	GCCCCAGAAG[G/A]ACCTGAGCAG	M	G	A	D	N
				mitogen-activated,
				p38Beta (MAP kinase
				p38Beta)
G610u4	WIAF-12282	HT48690	439	protein kinase,	TCCTGGTTTA[C/T]CAGCTCCTGC	S	C	T	Y	Y
				mitogen-activated,
				p38Beta (MAP kinase
				p38Beta)
G612u1	WIAF-12344	HT1436	1513	RAF1, v-raf-1	TTTGCATGCA[A/G]AGAACATCAT	M	A	G	K	E
				murine leukemia
				viral oncogene
				homolog 1
G614u1	WIAF-12267	HT321	603	BRAF, v-raf murine	GACAGTCTAA[A/G]GAAAGCACTG	M	A	G	K	R
				sarcoma viral
				oncogene homolog 51
G614u2	WIAF-12268	HT321	2282	BRAF, v-raf murine	CCAAACAGAG[G/A]ATTTTAGTCT	M	G	A	D	N
				sarcoma viral
				oncogene homolog 51
G614u3	WIAF-12299	HT321	973	BRAF, v-raf murine	AGGAAGAGGC[G/A]TCCTTAGCAC	S	G	A	A	A
				sarcoma viral
				oncogene homolog 51
G616u1	WIAF-12253	HT48746	498	TRAF-interacting	AAGAAGACAA[G/T]AGGTTTCTTC	N	G	T	E	*
				protein (I-TRAF)
G616u2	WIAF-12269	HT48746	1338	TRAF-interacting	GCATATACCT[C/G]GAGTATGTGA	M	C	G	R	G
				protein (I-TRAF)
G616u3	WIAF-12285	HT48746	377	TRAF-interacting	ATAACAATTA[T/C]GGCTGTGTCC	S	T	C	Y	Y
				protein (I-TRAF)
G616u4	WIAF-12288	HT48746	1032	TRAF-interacting	TGAAATTCAG[G/A]GAATTGACCC	M	G	A	G	R
				protein (I-TRAF)
G617u1	WIAF-12256	HT1614	52	PPP1CA, protein	GAAGCTCAAC[C/T]TGGACTCGAT	S	C	T	L	L
				phosphatase 1,
				catalytic subunit,
				alpha isoform
G617u2	WIAF-12270	HT1614	792	PPP1CA, protein	AAGACGGCTA[C/T]GAGTTCTTTG	S	C	T	Y	Y
				phosphatase 1,
				catalytic subunit,
				alpha isoform
G618u1	WIAF-12238	HT27508	1598	protein	CATTGAACCA[A/C]CACAGTTCAA	M	A	C	T	P
				phosphatase, 2A
				B56-alpha
				subunit
G618u2	WIAF-12271	HT27508	1135	protein	ATCAGAAATT[C/T]GTACAACAGC	S	C	T	F	F
				phosphatase, 2A
				B56-alpha
				subunit
G62u1	WIAF-10369	HT0855	214	ERCC6, excision	AGGAGTACCT[G/C]TCCTTTCGTT	S	G	C	L	L
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G62u2	WIAF-10370	HT0855	926	ERCC6, excision	AAAACTGTCT[T/C]TTGAAAGGAA	M	T	C	F	L
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G62u3	WIAF-10428	HT0855	2904	ERCC6, excision	AGCACGGACA[C/T]GCAGGCCCGG	M	C	T	T	M
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G62u4	WIAF-10430	HT0855	3368	ERCC6, excision	TGACCCTCAC[A/G]TGAGTAGTAA	M	A	G	M	V
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G62u5	WIAF-10451	HT0855	1376	ERCC6, excision	TTCTGGGGAA[G/A]AAGCTGAAGC	M	G	A	E	K
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G62u6	WIAF-10452	HT0855	3716	ERCC6, excision	TAAGCATTGC[A/G]GACACGCCAA	M	A	G	R	G
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G62u7	WIAF-10453	HT0855	3967	ERCC6, excision	CCCTGAAAGC[A/C]CTGAGGCTCT	S	A	C	A	A
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G62u8	WIAF-10454	HT0855	4016	ERCC6, excision	TGGTGTTCCC[A/G]CCTGGACTGG	M	A	G	T	A
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G62u9	WIAF-10455	HT0855	3979	ERCC6, excision	TGAGGCTCTC[T/C]CGTCAGCGGT	S	T	C	S	S
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G62u10	WIAF-10456	HT0855	3729	ERCC6, excision	GACCCCAAGT[T/C]TGAAGGAACT	M	T	G	F	C
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G62u11	WIAF-10476	HT0855	1275	ERCC6, excision	TCTGGAGATG[G/A]TACTGACTAT	M	G	A	G	D
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G62u12	WIAF-10477	HT0855	2017	ERCC6, excision	TGATCTTGGA[C/T]GAAGGACACA	S	C	T	D	D
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G62u13	WIAF-10479	HT0855	3265	ERCC6, excision	CTAACATATC[T/C]CTAAATCATG	S	T	C	S	S
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G62u14	WIAF-10481	HT0855	4317	ERCC6, excision	GGGCACCTGC[A/G]GGAAGCTTCT	M	A	G	Q	R
				repair cross-
				complementing rodent
				repair deficiency,
				complementation
				group 6
G620a1	WIAF-12116	HT1943	1256	PPP2CB, protein	TATCATGGAA[T/A]TAGATGACAC	M	T	A	L	I
				phosphatase 2
				(formerly 2A),
				catalytic subunit,
				beta isoform
G620a2	WIAF-12117	HT1943	1326	PPP2CB, protein	CCTCATGTTA[C/G]ACGGCGCACC	M	C	G	T	R
				phosphatase 2
				(formerly 2A),
				catalytic subunit,
				beta isoform
G620u3	WIAF-12239	HT1943	819	PPP2CB, protein	TTTTATGATG[A/G]ATGTCTGCGA	M	A	G	E	G
				phosphatase 2
				(formerly 2A),
				catalytic subunit,
				beta isoform
G623u1	WIAF-12260	HT3979	459	PPP1CB, protein	TTCATCGACA[A/G]TATACACATT	S	A	G	Q	Q
				phosphatase 1,
				catalytic subunit,
				beta isoform
G625u1	WIAF-12266	HT1951	2279	PPP2R2A, protein	CATTCTGGAG[A/G]ATTACTAGCA	M	A	G	E	G
				phosphatase 2
				(formerly 2A),
				regulatory subunit
				(PR 52), alpha
				isoform
G628a1	WIAF-12104	HT2780	1104	PPP1CC, protein	AGGGGTATGA[T/A]CACAAAGCAA	M	T	A	I	N
				phosphatase 1,
				catalytic subunit,
				gamma isoform
G628a2	WIAF-12105	HT2780	973	PPP1CC, protein	CCAATTATTG[C/T]GGACAGTTTG	S	C	T	C	C
				phosphatase 1,
				catalytic subunit,
				gamma isoform
G628u3	WIAF-12311	HT2780	888	PPP1CC, protein	GATCTTATAT[G/T]TAGAGCCCAT	M	A	T	C	P
				phosphatase 1,
				catalytic subunit,
				gamma isoforn
G630a1	WIAF-12103	HT5086	704	protein phosphatase	AAAGATGCAG[A/G]TCTGAACTCT	M	A	G	D	G
				2A, 130 kDa
				regulatory subunit
G630a2	WIAF-12106	HT5086	1015	protein phosphatase	CGATGGGAAC[G/T]CCCCATCCTT	M	G	T	A	S
				2A, 130 kDa
				regulatory subunit
G630a3	WIAF-12107	HT5086	1024	protein phosphatase	CGCCCCATCC[T/c]TTGGTTTACT	M	T	c	F	L
				2A, 130 kDa
				regulatory subunit
G630a4	WIAF-12108	HT5086	837	protein phosphatase	ACTTAAAGGA[T/C]ATTGCAGGAG	S	T	C	D	D
				2A, 130 kDa
				regulatory subunit
G630u5	WIAF-12325	HT5086	1200	protein phosphatase	TAAAGATGTG[C/T]TTGGACATCT	S	C	T	C	C
				2A, 130 kDa
				regulatory subunit
G630u6	WIAF-12326	HT5086	2810	protein phosphatase	ATGTTCAGGG[C/TITGCAGGGGGA	M	C	T	A	V
				2A, 130 kDa
				regulatory subunit
G630u7	WIAF-12351	HT5086	512	protein phosphatase	ATTATGGCAG [C/T]AACTTACAGA	M	C	T	A	V
				2A, 130 kDa
				regulatory subunit
G630u8	WIAF-12352	HT5086	703	protein phosphatase	CAAACATGCA[G/A]ATCTGAACTC	M	G	A	D	N
				2A, 130 kDa
				regulatory subunit
G630u9	WIAF-12353	HT5086	1069	protein phosphatasa	ACCTTTGTCT[C/T]ATAGAAACTC	M	C	T	H	Y
				2A, 130 kDa
				regulatory subunit
G634u1	WIAF-11825	X04434	2283	IGF1R, insulin-	TGCAAGTGGC[C/T]AACACCACCA	S	C	T	A	A
				like growth factor
				1 receptor
G634u2	WIAF-11826	X04434	2279	IGF1R, insulin-	GTCATGCAAG[T/C]GGCCAACACC	M	T	C	V	A
				like growth factor
				1 receptor
G634u3	WIAF-11781	X04434	1731	IGF1R, insulin-	ACAAGGACGT[G/AIGAGCCCGGCA	S	G	A	V	V
				like growth factor
				1 receptor
G634a4	WIAF-13106	X04434	948	IGF1R, insulin-	TCCACGACGG[C/A]GAGTGCATGC	S	C	A	G	G
				like growth factor
				1 receptor
G634a5	WIAF-13107	X04434	1089	IGF1R, insulin-	CTTCTGCTCA[G/C]ATGCTCCAAG	M	G	C	Q	H
				like growth factor
				1 receptor
G634a6	WIAF-13108	X04434	2539	IGF1R, insulin-	AGAAGGAGCA[G/A]ATGACATTCC	M	G	A	D	N
				like growth factor
				1 receptor
G634a7	WIAF-13109	X04434	2606	IGF1R, insulin-	AAGTGGCCGG[A/C]ACCTGACAAT	M	A	C	E	A
				like growth factor
				1 receptor
G634a8	WIAF-13111	X04434	1543	IGF1R, insulin-	CTCCACCACC[A/T]CGTCGAAGAA	M	A	T	T	S
				like growth factor
				1 receptor
G634a9	WIAF-13112	X04434	1549	IGF1R, insulin-	CACCACGTCG[A/G]AGAATCGCAT	M	A	G	K	E
				like growth factor
				1 receptor
G634a10	WIAF-13113	X04434	1596	IGF1R, insulin-	CCCCTGACTA[C/T]AGGGATCTCA	S	C	T	Y	Y
				like growth factor
				1 receptor
G645u1	WIAF-12332	HT5191	1127	retinoic acid-	TCTGCAGACT[C/T]TTCAGGAGAG	M	C	T	L	F
				binding protein II
G645u2	WIAF-12333	HT5191	1048	retinoic acid-	AAGCATTAGA[G/A]GCCTTACAGA	S	G	A	E	E
				binding protein II
G646u1	WIAF-12303	X81479	1204	EMR1, egf-like	CAAATATCCA[T/C]GTGGACTAAA	M	T	C	M	T
				module containing,
				mucin-like,
				hormone receptor-
				like sequence 1
G646u2	WIAF-12304	X81419	1919	EMR1, egf-like	TTCTGCTGTG[T/G]CGCTCCATCC	M	T	G	C	W
				module containing,
				mucin-like,
				hormone receptor-
				like sequence 1
G646u3	WIAF-12316	X81479	590	EMR1, egf-like	CTTGCCCAGA[G/T]CATGCAACTT	M	G	T	E	D
				module containing,
				mucin-like,
				hormone receptor-
				like sequence 1
G646u4	WIAF-12317	X81479	799	EMR1, egf-like	GCACCAAGCA[G/A]TGGACAGTTG	M	G	A	S	N
				module containing,
				mucin-like,
				hormone receptor-
				like sequence 1
G646u5	WIAF-12318	X81479	558	EMR1, egf-like	TGAAGACGTG[A/G]ATGAATGTGC	M	A	G	N	D
				module containing,
				mucin-like,
				hormone receptor-
				like sequence 1
G646u6	WIAF-12334	X81479	207	EMR1, egf-like	TTACTATTGC[A/G]CTTGCAAACA	M	A	G	T	A
				module containing,
				mucin-like,
				hormone receptor-
				like sequence 1
G646u7	WIAF-12335	X81479	458	EMR1, egf-like	TCACCAGCAG[G/C]GTCTGCCCTG	M	G	C	R	S
				module containing,
				mucin-like,
				hormone receptor-
				like sequence 1
G646u8	WIAF-12336	X81479	1308	EMR1, egf-like	CTCAGCAAAT[G/A]TCACTCCGGC	M	G	A	V	I
				module containing,
				mucin-like,
				hormone receptor-
				like sequence 1
G646u9	WIAF-12337	X81479	1285	EMR1, egf-like	ACACTGGCAT[C/T]TTTTTGGAAA	M	C	T	S	F
				module containing,
				mucin-like,
				hormone receptor-
				like sequence 1
G646u10	WIAF-12338	X81479	2026	EMR1, egf-like	GACAACAAGA[C/T]GGGCTGCGCC	M	C	T	T	M
				module containing,
				mucin-like,
				hormone receptor-
				like sequence 1
G647u1	WIAF-12339	HT5190	174	RARA, retinoic acid	TGCCTCCCTA[C/T]GCCTTCTTCT	S	C	T	Y	Y
				receptor, alpha
G648a1	WIAF-13332	HT0070	469	retinoic acid	AACCTGAGCC[A/G]CGACCAGCGT	—	A	G	—	—
				receptor, beta
G648a2	WIAF-13333	HT0070	532	retinoic acid	ATTGTTTTTA[A/G]GGTGAGAAAT	—	A	G	—	—
				receptor, beta
G6S0u1	WIAF-12323	X52773	862	RXRA, retinoid X	CTCGCCGAAC[G/A]ACCCTGTCAC	M	G	A	D	N
				receptor, alpha
G650u2	WIAF-12341	X5277	3102	RXRA, retinoid X	TCCTGCCGCT[C/T]GATTTCTCCA	S	C	T	L	L
				receptor, alpha
G650u3	WIAF-12348	X5277	3673	RXRA, retinoid X	GGCCATCGGC[A/C]TGAAGCGGCA	M	A	G	M	V
				receptor, alpha
G650u4	WIAF-12349	X52773	902	RXRA, retinoid X	GACAAACACC[T/C]TTTCACCCTC	M	T	C	L	P
				receptor, alpha
G653a1	WIAF-13326	HT1458	439	RARB, retinoic	AGGACAAAGC[T/C]CTCAAAGCAT	S	T	C	A	A
				acid receptor,
				beta
G655a1	WIAF-13327	J05252	1158	PCSK2, proprotein	CCTTCACGAA[C/T]GGGAGGAAAA	S	C	T	N	N
				convertase
				subtilisin/kexin
				type 2
G655a2	WIAF-13334	J05252	678	PCSK2, proprotein	CCTATCCTTA[C/A]CCTCCCTACA	N	C	A	Y	*
				convertase
				subtilisin/kexin
				type 2
G655a3	WIAF-13335	J05252	744	PCSK2, proprotein	TTTCTGCTCC[C/T]GCCAACAACA	S	C	T	A	A
				convertase
				subtilisin/kexin
				type 2
G658u1	WIAF-11856	J02943	971	CBG, corticosteroid	TCTATGACCT[T/C]CGAGATGTCC	S	T	C	L	L
				binding globulin
G658u2	WIAF-13407	J02943	771	CBG, corticosteroid	CCTTCATGAC[T/C]CACAGCTCCC	M	T	G	S	A
				binding globulin
G658u3	WIAF-13408	J02943	773	CBG, corticosteroid	TTCATCACTC[A/G]GAGCTCCCCT	S	A	G	S	S
				binding globulin
G658u4	WIAF-13409	J02943	1046	CBG, corticosteroid	TCACCCAGGA[C/T]GCCCAGCTCA	S	C	T	D	D
				binding globulin
G663u1	WIAF-13400	HT3157	1202	TPO, thyroid	CGCCACGCGC[G/A]CCTGCGGCCT	S	G	A	A	A
				peroxidase
G663u2	WIAF-13401	HT3157	1282	TPO, thyroid	GGCCGCGCCA[G/C]CGAGGTCCCC	M	G	C	S	T
				peroxidase
G668a1	WIAF-13350	U53506	350	DI02, deiodinase,	TCGATGCCTA[C/A]AAACAGGTGA	N	C	A	Y	*
				iodothyronine,
				type II
G668a2	WIAF-13351	U53506	354	DI02, deiodinase,	TGCCTACAAA[C/A]AGGTGAAATT	M	C	A	Q	K
				iodothyronine,
				type II
G668a3	WIAF-13352	U53506	408	DI02, deiodinase,	TGTCTCGACT[A/G]CAGAAGGAGG	M	A	G	T	A
				iodothyronine,
				type II
G673a1	WIAF-13328	M57464	1723	Human ret proto-	CGAGCCTGGC[C/A]AGCCCCGGGG	M	G	A	E	K
				oncogene mRNA for
				tyrosine kinase.
G673a2	WIAF-13338	M57464	1186	Human ret proto-	GGCTCGCCCA[T/A[TTGCCCAGAT	M	T	A	F	I
				oncogene mRNA for
				tyrosine kinase.
G673a3	WIAF-13337	M57464	1227	Hunan ret proto-	ACTGCCAGGC[G/A]TTCACTCGGA	S	G	A	A	A
				oncogene mRNA for
				tyrosine kinase.
G673a4	WIAF-13338	M57464	2118	Human ret proto-	TTGGAAAAAC[T/A]CTAGGAGAAG	S	T	A	T	T
				oncogene mRNA for
				tyrosine kinase.
G673a5	WIAF-13339	M57464	2238	Human ret proto-	CGAGTGAGCT[T/C]CGAGACCTGC	S	T	G	L	L
				oncogene mRNA for
				tyrosine kinase.
G678a1	WIAF-13353	D49492	1439	GDF10, growth	TCGGCTGGAA[T/A]GAATGCATAA	M	T	A	N	K
				differentiation
				factor 10
G55u1	WIAF-10434	HT1115	1214	ERCC3, excision	CTGTGGAGCA[G/A]TGGAAAGCCC	S	G	A	Q	Q
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 3 (xeroderma
				pigmentosum group B
				complementing)
G68u2	WIAF-10435	HT1115	1155	ERCC3, excision	TGTGACTGCT[G/C]CATGCACTGT	M	G	C	A	P
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 3 (xeroderma
				pigmentosum group B
				complementing)
G68u3	WIAF-10436	HT1115	1327	ERCC3, excision	AGCACCTACT[C/T]CATCCTGGGC	M	C	T	S	F
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 3 (xeroderma
				pigmentosum group B
				complementing)
G68u4	WIAF-10461	HT1115	926	ERCC3, excision	AGGAAATCAT[T/C]CACGAACTCC	S	T	C	I	I
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 3 (xeroderma
				pigmentosum group B
				complementing)
G68u5	WIAF-10464	HT1115	1430	ERCC3, excision	AAGTGCACAC[C/T]ATACCAGCCA	S	C	T	T	T
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 3 (xeroderma
				pigmentosum group B
				complementing)
G684a1	WIAF-13359	X51801	712	BMP7, bone morpho-	GTTTATCACG[T/G]GCTCCACCAG	M	T	G	V	G
				genetic protein
				7 (osteogenic
				protein 1)
G684a2	WIAF-13360	X51801	719	BMP7, bone morpho-	AGGTCCTCCA[G/A]GAGCACTTGG	S	G	A	Q	Q
				genetic protein
				7 (osteogenic
				protein 1)
G684a3	WIAF-13361	X51801	796	BMP7, bone morpho-	GGCTGGCTGG[T/G]GTTTCACATC	M	T	G	V	G
				genetic protein
				7 (osteogenic
				protein 1)
G684a4	WIAF-13362	X51803	862	BMP7, bone morpho-	GGCCTGCAGC[T/G]CTCGGTGGAG	M	T	G	L	R
				genetic protein
				7 (osteogenic
				protein 1)
G684a5	WIAF-13363	X51801	658	BMP7, bone morpho-	ATCTACAAGG[A/G]CTACATCCGC	M	A	G	D	G
				genetic protein
				7 (osteogenic
				protein 1)
G684u6	WIAF-13834	X51801	1421	BMP7, bone morpho-	GCCACTAGCT[C/T]CTCCCAGAAT	—	C	T	—	—
				genetic protein
				7 (osteogenic
				protein 1)
G685a1	WIAF-13329	D89675	882	BMPR1B, bone	GTTCCCTTTA[T/G]GATTATCTGA	N	T	G	Y	*
				morphogenetic
				protein receptor,
				type IB
G685a2	WIAF-13330	D89675	920	BMPR1B, bone	GCTAAATCAA[T/C]GCTGAAGTTA	M	T	C	M	T
				morphogenetic
				protein receptor,
				type IB
G685a3	WIAF-13331	D89675	770	BMPR1B, bone	TATCACACAG[T/C]GTTCATGAGG	M	T	G	V	G
				morphogenetic
				protein receptor,
				type IB
G685a4	WIAF-13340	D89675	1303	BMPR1B, bone	TCCTTATCAT[C/A]ACCTACTGCC	M	G	A	D	N
				morphogenetic
				protein receptor,
				type IB
G685a5	WIAF-13341	D89675	1372	BMPR1B, bone	GTTACCCCCC[T/G]CATTCCCAAA	M	T	G	S	A
				morphogenetic
				protein receptor,
				type IB
G685a6	WIAF-13342	D89675	1173	BMPR1B, bone	TGTTGGACGA[C/A]AGCTTGAACA	S	G	A	E	E
				morphogenetic
				protein receptor,
				type IB
G686u1	WIAF-13816	Z48923	2705	BMPR2, bone	AAATTTGGCA[G/A]CAAGCACAAA	M	G	A	S	N
				morphogenetic
				protein
				receptor, type
				II (serine/
				threonine kinase)
G686u2	WIAF-13817	Z48923	2749	BMPR2, bone	TGGAGTTGCC[A/T]AGATGAATAC	N	A	T	K	*
				morphogenetic
				protein
				receptor, type II
				(serine/threonine
				kinase)
G687a1	WIAF-13343	HT1455	626	CALB1, calbindin 1,	ATGATCACGA[C/T]GGCAATCCAT	S	C	T	D	D
				(28 kD)
G696u1	WIAF-11839	HT27700	1075	calcium-sensing	GCCCACAATT[G/C]CACCTGATGA	M	G	C	A	P
				receptor
G696u2	WIAF-11840	HT27700	1551	calcium-sensing	TACCTGTGGA[C/T]ACCTTTCTGA	S	C	T	D	D
				receptor
G696u3	WIAF-11841	HT27700	1688	calcium-sensing	TTACGGATAT[C/T]CTACAATGTG	M	C	T	S	F
				receptor
G696u4	WIAF-11842	HT27700	1698	calcium-sensing	CCTACAATGT [G/T]TACTTACCAG	S	G	T	V	V
				receptor
G696u5	WIAF-11858	HT27700	1767	calcium-sensing	GGAGAGGGCT[C/T]TTCACCAATG	S	C	T	L	L
				receptor
G696u6	WIAF-118S9	HT27700	1689	calcium-sensing	TACGCATATC[C/T]TACAATGTGT	S	C	T	S	S
				receptor
G696u7	WIAF-11860	HT27700	2541	calcium-sensing	TCGTCCTCTG[C/T]ATCTCATCCA	S	C	T	C	C
				receptor
G696u8	WIAF-11861	HT27700	2581	calcium-sensing	TGTCCTCCTG[G/A]TGTTTGAGGC	M	G	A	V	M
				receptor
G696u9	WIAF-11863	HT27700	3159	calcium-sensing	TCTCCCGCAA[G/C]CGGTCCAGCA	M	G	C	K	N
				receptor
G696u10	WIAF-11872	HT27700	562	calcium-sensing	TCCTATTCAT[T/AJTTCGAGTACC	M	T	A	F	I
				receptor
G696u11	WIAF-11878	HT27700	2941	calcium-sensing	CATTCCAGCC[T/G]ATGCCAGCAC	M	T	G	Y	D
				receptor
G696u12	WIAF-13386	HT27700	1145	calcium-sensing	AGGGATATCT[G/A]CATCGACTTC	M	G	A	C	Y
				receptor
G696u13	WIAF-13395	HT27700	670	calcium-sensing	CATATTTGCC[A/GJTAGAGGACAT	M	A	G	I	V
				receptor
G696u14	WIAF-13396	HT27700	2243	calcium-sensing	TTCTGGTCCA[A/G]TGAGAACCAC	M	A	G	N	S
				receptor
G696u15	WIAF-13397	HT27700	2742	calcium-sensing	AGCTGGAGGA[T/C]GAGATCATCT	S	T	C	D	D
				receptor
G698u1	WIAF-13547	X61598	393	CBP1, collagen-	TCAGCAACTC[G/C]ACGGCGCGCA	S	G	C	S	S
				binding protein 1
G698u2	WIAF-13549	X61598	628	CBP1, collagen-	CGGCGCCCTG[C/T]TAGTCAACGC	S	C	T	L	L
				binding protein 1
G698u3	WIAF-13550	X61598	1230	CBP1, collagen-	GCGGCTCCCT[G/A]CTATTCATTG	S	G	A	L	L
				binding protein 1
G701u1	WIAF-12382	HT27657	706	CGRP type I	AACGATGTTG[C/A]AGCAGGAACT	M	C	A	A	E
				receptor
G701u2	WIAF-12391	HT27657	841	CGRP type I	TGGACAAATT[A/T]TACCCAGTGT	M	A	T	Y	F
				receptor
G704u1	WIAF-14046	X60382	1396	COL10A1, collagen,	AGGCATTCCA[G/A]GATTCCCTGG	M	G	A	G	R
				type X, alpha
				1 (Schmid meta-
				physeal chondro-
				dysplasia)
G704u2	WIAF-14070	X60382	1648	COL10A1, collagen,	TGCCAACCAG[G/C]CGGTAACAGC	M	G	C	G	R
				type X, alpha
				1 (Schmid meta-
				physeal chondro-
				dysplasia)
G704u3	WIAF-14071	X60382	1824	COL10A1, collagen,	CATACCACGT[G/C]CATCTGAAAG	S	G	C	V	V
				type X, alpha
				1 (Schmid meta-
				physeal chondro-
				dysplasia)
G704u4	WIAF-14072	X60382	1582	COL10A1, collagen,	AGTCATCCCT[C/C]ACGGTTTTAT	M	G	C	E	Q
				type X, alpha
				1 (Schmid meta-
				physeal chondro-
				dysplasia)
G705a1	WIAF-13228	J04177	686	COL11A1, collagen,	ACAACAAAAC[T/A]GTCACAATCA	S	T	A	T	T
				type XI, alpha 1
G705a2	WIAF-13229	J04177	698	COL11A1, collagen,	TGACAATCAT[T/A]GTTGATTGTA	S	T	A	I	I
				type XI, alpha 1
G705a3	WIAF-13230	J04177	8881	COL11A1, collagen,	TACTCCACAC[T/A]CTGACTCTTC	M	T	A	C	S
				type XI, alpha 1
G705a4	WIAF-13231	J04177	894	COL11A1, collagen,	AGACTGTGAC[T/A]CTTCAGCACC	M	T	A	S	T
				type XI, alpha 1
G705a5	WIAF-13232	J04177	651	COL11A1, collagen,	TGACCGCAAG[T/A]CCCATCCCCT	M	T	A	W	R
				type XI, alpha 1
G705a6	WIAF-13233	J04177	661	COL11A1, collagen,	TGGCATCGGG[T/A]AGCAATCAGC	M	T	A	V	E
				type XI, alpha 1
G705a7	WIAF-13234	J04177	1597	COL11A1, collagen,	CGTCCTGGCT[T/C]ACCAGGGGCT	M	T	C	L	S
				type XI, alpha 1
G705a8	WIAF-13235	J04177	2745	COL11A1, collagen,	TGGGTTTCCA[C/A]GTGCCAATGG	M	G	A	G	S
				type XI, alpha 1
G705a9	WIAF-13236	J04177	4385	COL11A1, collagen,	GTCCAGAAGG[T/A]CTTCGGGGCA	S	T	A	G	G
				type XI, alpha 1
G705a10	WIAF-13237	J04177	4576	COL11A1, collagen,	GAAAAAGGTG[A/T]CCGAGGGGTC	M	A	T	D	V
				type XI, alpha 1
G705a11	WIAF-13238	J04177	4306	COL11A1, collagen,	GCTAAGGGGG[A/C]AGCAGGTCCA	M	A	C	E	A
				type XI, alpha 1
G705a12	WIAF-13239	J04177	4837	COL11A1, collagen,	AGACATACTG[A/G]AGGCATGCAA M	A	G	E	G
				type XI, alpha 1
G705a13	WIAF-13240	J04177	4931	COL11A1, collagen,	AACAAGACAT[C/T]CACCATATGA	S	C	T	I	I
				type XI, alpha 1
G705a14	WIAF-13346	J04177	299	COL11A1, collagen,	AAGCACTAGA[T/G]TTTCACAATT	M	T	G	D	E
				type XI, alpha 1
G705a15	WIAF-13347	J04177	2225	COL11A1, collagen,	GGGAGCCTGG[G/C]CCTCCAGGTC	S	G	C	G	G
				type XI, alpha 1
G705u16	WIAF-13679	J04177	5493	COL11A1, collagen,	AATTCATCAA[G/A]TACCTATTGT	M	G	A	V	I
				type XI, alpha 1
G705u17	WIAF-13700	J04177	3484	COL11A1, collagen,	GGACTTCAAG[G/A]TCCTGTTGGT	M	G	A	G	D
				type XI, alpha 1
G705u18	WIAF-13709	J04177	5392	COL11A1, collagen,	GACATGTCCT[A/T]TGACAATAAT	M	A	T	Y	F
				type XI, alpha 1
G707u1	WIAF-12363	U32169	4996	COL11A2, collagen,	TCCCCTGAGA[C/T]TCCGTGGGGC	M	C	T	L	F
				type XI, alpha 2
G707u2	WIAF-12374	U32169	3580	COL11A2, collagen,	CAATGGCCCT[C/A]ATGGCCCACA	M	G	A	D	N
				type XI, alpha 2
G707u3	WIAF-12385	U32169	2059	COL11A2, collagen,	GCCTGGCTCA[C/A]ACGGACCCCC	M	G	A	D	N
				type XI, alpha 2
G708a1	WIAF-13354	U73778	1885	COL12A1, collagen,	GCCTCTCCTC[C/T]TCCACAGACC	M	C	T	P	L
				type XII,
				alpha 1
G708a2	WIAF-13355	U73778	3630	COL12A1, collagen,	TGTTGGACAA[C/A]AAATGACAAC	M	G	A	E	K
				type XII,
				alpha 1
G708a3	WIAF-13356	U73778	3905	COL12A1, collagen,	GCTTCTTGCA[A/T]GCTCTGGCAA	M	A	T	Q	H
				type XII,
				alpha 1
G708a4	WIAF-13357	U73778	7051	COL12A1, collagen,	ATTCCACCAG[C/A]CCGGGATGTA	M	C	A	A	D
				type XII,
				alpha 1
G708a5	WIAF-13358	U73778	8036	COL12A1, collagen,	AAGAAGTAAA[C/A]ACATTATTTT	S	G	A	K	K
				type XII,
				alpha 1
G708a6	WIAF-13364	U73778	1461	COL12A1, collagen,	TGGCTCCTAT[A/T]GCATTGGGAT	M	A	T	S	C
				type XII,
				alpha 1
G708a7	WIAF-13365	U73778	2344	COL12A1, collagen,	ATTACTTGGA[C/T]TCAAGCTCCA	M	C	T	T	I
				type XII,
				alpha 1
G708a8	WIAF-13366	U73778	5207	COL12A1, collagen,	CAGATAAGAT[C/A]GAGACCATCT	M	G	A	M	I
				type XII,
				alpha 1
G708a9	WIAF-13367	U73778	6592	COL12A1, collagen,	GAGCCCATGG[A/T]AGCCTTTGTT	M	A	T	E	V
				type XII,
				alpha 1
G708a10	WIAF-13368	U73778	7434	COL12A1, collagen,	CCAGGATGAG[G/A]TCAACAAGGC	M	G	A	V	I
				type XII,
				alpha 1
G708a11	WIAF-13369	U73778	9108	COL12A1, collagen,	ACCTCGGGGG[C/G]TGCCTGGGCC	M	C	G	L	V
				type XII,
				alpha 1
G708a12	WIAF-13370	U73778	9111	COL12A1, collagen,	TCGGGGGCTG[C/T]CTGGGCCCCC	M	C	T	P	S
				type XII,
				alpha 1
G708a13	WIAF-13371	U73778	9196	COL12A1, collagen,	CCCCCTGGCC[G/A]TCCTGGAAAC	M	G	A	R	H
				type XII,
				alpha 1
G708u14	WIAF-13972	U73778	3044	COL12A1, collagen,	CAGTATTTGC[C/A]ACTTACAGCA	S	C	A	A	A
				type XII,
				alpha 1
G708u15	WIAF-13977	U73778	5853	COL12A1, collagen,	TCTGACTCTA[G/C]TTCCCGTTTA	M	G	C	V	L
				type XII,
				alpha 1
G710u1	WIAF-12371	D38163	3082	COL19A1, collagen,	AGGAAACAAG[C/T]GCTCCATGGG	M	G	T	G	C
				type XIX,
				alpha 1
G710u2	WIAF-12388	D38163	2089	COL19A1, collagen,	TCCAGGGACT[C/T]CAGGCAATGA	M	C	T	P	S
				type XIX,
				alpha l
C711u1	WIAF-12360	L25286	1449	COL15A1, collagen,	TGTGGGTCCA[A/C]GCACTCAACA	M	A	G	S	G
				type XV, alpha 1
C711u2	WIAF-12372	L25286	4001	COL15A1, collagen,	ATATTCCAAT[A/C]TACTCCTTTC	M	A	G	I	M
				type XV, alpha
				1
G711u3	WIAF-12373	L25286	3867	COL15A1, collagen,	CCATTTGCAA[G/T]ATCTGTCCAC	M	G	T	D	Y
				type XV, alpha
				1
C711a4	WIAF-13372	L25286	395	COL15A1, collagen,	CCACCAGCAC[C/T]CGTGCTGCCG	S	C	T	T	T
				type XV, alpha
				1
C711a5	WIAF-13373	L25286	3101	COL15A1, collagen,	AAGGCGACCA[G/A]GGACCCCAGG	S	G	A	Q	Q
				type XV, alpha
				1
G712u1	WIAF-13619	M92642	3608	COL16A1, collagen,	GGCGACCAGG[C/A]ATTTCAAGGC	M	G	A	G	E
				type XVI,
				alpha 1
G712u2	WIAF-13620	M92642	4944	COL16A1, collagen,	CCATGAAAAC[C/T]ATGAAGGGGC	S	C	T	T	T
				type XVI,
				alpha 1
G712u3	WIAF-13621	M92642	4707	COL16A1, collagen,	CCAAACGTCA[A/C]AAAGGGGACA	M	A	C	E	D
				type XVI,
				alpha 1
G712u4	WIAF-13654	M92642	421	COL16A1, collagen,	GCCCACGCCA[C/A]GAGTATTCCC	S	C	A	R	R
				type XVI,
				alpha 1
G712u5	WIAF-13655	M92642	444	COL16A1, collagen,	GGGGTCTCCC[G/A]GAGGAGTTTG	S	G	A	P	P
				type XVI,
				alpha 1
G712u6	WIAF-13656	M92642	338	COL16A1, collagen,	CTCATGAAGA[A/C]GTCTGCCATC	M	A	C	K	T
				type XVI,
				alpha 1
G712u7	WIAF-13862	M92642	3227	COL16A1, collagen,	CCTGGTCCTC[C/T]GGGATTCCCA	M	C	T	P	L
				type XVI,
				alpha 1
G712u8	WIAF-13863	M92642	3199	COL16A1, collagen,	TCCTGGCTGT[G/T]TTGGGAGCCC	M	G	T	V	F
				type XVI,
				alpha 1
G712u9	WIAF-13878	M92642	318	COL16A1, collagen,	ACCTCATCCA[C/T]CGACTCAGCC	S	C	T	H	H
				type XVI,
				alpha 1
G712u10	WIAF-13882	M92642	1346	COL16A1, collagen,	ACAGGCGAGA[A/G]GGGCCAGAAA	M	A	G	K	R
				type XVI,
				alpha 1
G712u11	WIAF-13883	M92642	1309	COL16A1, collagen,	GTCACGACCT[C/T]TGGGACCCTC	S	C	T	L	L
				type XVI,
				alpha 1
G715a1	WIAF-13344	Z74615	3504	COL1A1, collagen,	TCCTGGTGAA[C/G]AAGGTCCCTC	M	C	G	Q	E
				type I, alpha 1
G717u1	WIAF-12639	Z74616	3988	COL1A2, collagen,	ATGAGGAGAC[T/C]GGCAACCTGA	S	T	C	T	T
				type I, alpha 2
G720u1	WIAF-12367	X14420	3494	COL3A1, collagen,	GGTGCAATCG[G/A]CAGTCCAGGA	M	G	A	G	D
				type III, alpha 1
				(Ehlers-Danlos
				syndrome type IV,
				autosomal dominant)
G720u2	WIAF-12383	X14420	3035	COL3A1, collagen,	GGTGTCAAGG[G/A]TGAAAGTGGG	M	G	A	G	D
				type III, alpha 1
				(Ehlers-Danlos
				syndrome type IV,
				autosomal dominant)
G720a3	WIAF-13374	X14420	214	COL3A1, collagen,	TCTTGGTCAG[T/C]CCTATGCGGA	M	T	C	S	P
				type III, alpha 1
				(Ehlers-Danlos
				syndrome type IV,
				autosomal dominant)
G720a4	WIAF-13375	X14420	1953	COL3A1, collagen,	CTGGACCTCA[A/G]GGACCCCCAG	S	A	G	Q	Q
				type III, alpha 1
				(Ehlers-Danlos
				syndrome type IV,
				autosomal dominant)
G720a5	WIAF-13376	X14420	2194	COL3A1, collagen,	TAGAGGTGGA[G/A]CTGGTCCCCC	M	G	A	A	T
				type III, alpha 1
				(Ehlers-Danlos
				syndrome type IV,
				autosomal dominant)
G720a6	WIAF-13377	X14420	3731	COL3A1, collagen,	GGGATTGGAG[G/A]TGAAAAAGCT	M	G	A	G	D
				type III, alpha 1
				(Ehlers-Danlos
				syndrome type IV,
				autosomal dominant)
G722u1	WIAF-14132	HT3162	140	COL4A2, collagen,	GAGATTGGCG[C/T]GACTGGTGAT	M	C	T	A	V
				type IV, alpha 2
G724a1	WIAF-12120	X81053	3892	COL4A4, collagen,	CTCGTGGAAA[G/A]AAAGGTCCCC	S	G	A	K	K
				type IV, alpha 4
G724a2	WIAF-12121	X81053	4187	COL4A4, collagen,	GAAAGGACCA[A/G]TGGGATTCCC	M	A	G	H	V
				type IV, alpha 4
G724a3	WIAF-12122	X81053	3802	COL4A4, collagen,	ATGATGTGGG[G/A]CCACCTGGTC	S	G	A	G	G
				type IV, alpha 4
G724a4	WIAF-12123	X81053	1838	COL4A4, collagen,	ACCAGGAAAG[C/A]ATGGTGCCTC	M	C	A	H	N
				type IV, alpha 4
G724u5	WIAF-12364	X81053	376	COL4A4, collagen,	CTGTTTGCCA[C/T[TGTCTTCCTG	S	C	T	H	H
				type IV, alpha
				4
G724u6	WIAF-12365	X81053	2018	COL4A4, collagen,	TCCAGGGGAT[C/G]ATGAACATGC	M	C	G	H	D
				type IV, alpha
				4
G724u7	WIAF-12366	X81053	4756	COL4A4, collagen,	GCCTTCCCCT[A/G]TTTACCACGC	S	A	G	V	V
				type IV, alpha
				4
G724u8	WIAF-12377	X81053	3595	COL4A4, collagen,	CTGGACCACC[A/G]GGGTGCCCAG	S	A	G	P	P
				type IV, alpha
				4
G724u9	WIAF-12378	X81053	3516	COL4A4, collagen,	GGAGCATCCG[C/C]ACACCAGGGC	M	G	C	G	A
				type IV, alpha
				4
G724u10	WIAF-12379	X81053	4288	COL4A4, collagen,	CTGGTCTTCC[A/G]GCTCCCAGAG	S	A	G	P	P
				type IV, alpha
				4
G724u11	WIAF-12380	X81053	5140	COL4A4, collagen,	GCCACTTTTT[C/A]GCAAATAAGT	M	C	A	F	L
				type IV, alpha
				4
G724u12	WIAF-12387	X81053	207	COL4A4, collagen,	GACTTCCCTG[C/T]GATGTGGTCT	—	C	T	—	—
				type IV, alpha
				4
G727u1	WIAF-12362	D90279	5135	COL5A1, collagen,	TTCAACGTTT[A/T]CTGCAACTTC	M	A	T	Y	F
				type V, alpha 1
G727u2	WIAF-12369	D90279	4686	COL5A1, collagen,	AACAGGGTAT[C/T]ACTGCTCCTT	S	C	T	I	I
				type V, alpha 1
G727u3	WIAF-12370	D90279	4608	COL5A1, collagen,	TCGGTCCTCC[G/C]GCTGAACAGG	S	G	C	P	P
				type V, alpha 1
G727a4	WIAF-13300	D90279	2034	COL5A1, collagen,	ACGGCCTGGC[T/A]GGGTTGCCAG	S	T	A	A	A
				type V, alpha 1
G727a5	WIAF-13301	D90279	2073	COL5A1, collagen,	GTGACCCTGG[T/C]CCTTCCGGCC	S	T	C	G	G
				type V, alpha 1
G727a6	WIAF-13302	D90279	3763	COL5A1, collagen,	CGGGCACAAA[G/A]GTGATGAAGG	M	G	A	G	S
				type V, alpha 1
G729u1	WIAF-11844	L02870	2345	COL7A1, collagen,	ATGGACTGGA[G/A]CCAGATACTG	S	G	A	E	E
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u2	WIAF-11845	L02870	3083	COL7A1, collagen,	TATCCTGGCG[G/A]CCACTCAGAG	S	G	A	R	R
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u3	WIAF-11846	L02810	3031	COL7A1, collagen,	GACTCGGTGA[C/T]TTTGGCCTGG	M	C	T	T	I
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u4	WIAF-11851	L02870	1289	COL7A1, collagen,	CGGACTATGA[G/T]GTGACCGTGA	M	G	T	E	D
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u5	WIAF-11852	L02870	1032	COL7A1, collagen,	CCAAGTGACT[G/T]TGATTGCCCT	M	G	T	V	L
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u6	WIAF-11853	L02870	1897	COL7A1, collagen,	CGCCGGGAGC[C/T]GGAAACTCCA	M	C	T	P	L
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u7	WIAF-11854	L02870	1827	COL7A1, collagen,	GCTTAGCTAC[A/T]CTGTGCGGGT	M	A	T	T	S
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u8	WIAF-11855	L02870	1893	COL7A1, collagen,	TGTCCGCCGG[G/A]AGCCCGAAAC	M	G	A	E	K
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u9	WIAF-11864	L02870	2142	COL7A1, collagen,	GGGCCCTGCT[G/A]CAGTCATCGT	M	G	A	A	T
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u10	WIAF-11865	L02870	2353	COL7A1, collagen,	GAGCCAGATA(C/T]TGAGTATACG	M	C	T	T	I
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u11	WIAF-11866	L02870	2221	COL7A1, collagen,	TCATCTGTCA[C/T]CATTACCTGG	M	C	T	T	I
				type VII, alpha
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u12	WIAF-11869	L02870	6585	COL7A1, collagen,	ACCAGGAGAG[C/T]GTGGTATGGC	M	C	T	R	C
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u13	WIAF-11870	L02870	8169	COL7A1, collagen,	GGGTGACCGA[G/T]GCTTTGACGG	M	G	T	G	C
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u14	WIAF-11877	L02870	438	COL7A1, collagen,	CGCCATCCGT[G/A]AGCTTAGCTA	M	G	A	E	K
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u15	WIAF-11882	L02870	3481	COL7A1, collagen,	AGGATCCGTG[A/T]CATGCCCTAC	M	A	T	D	V
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u16	WIAF-11883	L02870	5654	COL7A1, collagen,	ACGGAGAACC[T/C]GGGGACCCTG	S	T	C	P	P
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u17	WIAF-11884	L02870	7124	COL7A1, collagen,	TGCCAGGGCC[G/C]CGAGGCCAGA	S	G	C	P	P
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u18	WIAF-11885	L02870	7757	COL7A1, collagen,	CCTTGGATGG[T/C]GACAAAGGAC	S	T	C	G	C
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u19	WIAF-13389	L02870	1615	COL7A1, collagen,	ACCGTGGTTC[C/T]CACTGGACCA	M	C	T	P	L
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u20	WIAF-13390	L02870	2930	COL7A1, collagen,	TCCTAGGGCC[G/A]GCTGGAGAAG	S	G	A	P	P
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u21	WIAF-13399	L02870	5145	COL7A1, collagen,	CCAGCGACAT[C/T]CTGGACAGGA	M	C	T	P	S
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G729u22	WIAF-13411	L02870	3472	COL7A1, collagen,	ATCTTGCAAA[G/A]GATCCCTGAC	M	G	A	R	K
				type VII, alpha 1
				(epidermolysis
				bullosa, dys-
				trophic, dominant
				and recessive)
G730a1	WIAF-13303	X57527	305	COL8A1, collagen,	ATGGGCAAGG[A/G]AGCCGTTCCC	M	A	G	E	G
				type VIII,
				alpha 1
G732u1	WIAF-l26l6	M95610	936	COL9A2, collagen,	CACGGGCCAC[A/G]GCCCGGAACT	S	A	G	T	T
				type IX, alpha 2
G732u2	WIAF-12617	M95610	696	COL9A2, collagen,	AAGGGAGAGA[C/T]GGGCCCTCAT	S	C	T	D	D
				type IX, alpha 2
G732u3	WIAF-12619	M95610	1288	COL9A2, collagen,	AACTCGGTCA[C/T]CCAGCGCTCG	H	C	T	P	S
				type IX, alpha 2
G732u4	WIAF-12620	M95610	962	COL9A2, collagen,	CCACCAGCCC[C/G]TAGCGCCTCT	M	C	G	P	R
				type IX, alpha 2
G737u1	WIAF-13394	M13436	?	INHBA, inhibin,	TGCTCCCTG[G/T]	?	G	T
				beta A (activin
				A, activin AB alpha
				polypeptide)
G738a1	WIAF-13383	M58549	183	MGP, matrix Gla	ATGGAGAGCT[A/G]AAGTCCAAGA	M	A	G	K	E
				protein
G738a2	WIAF-13384	M58549	330	MGP, matrix Gla	GCGCCGAGGG[A/G]CCAAATGAGA	M	A	G	T	A
				protein
G739u1	WIAF-11867	U94332	862	TNFRSF11B, tumor	TGCTGAAGTT[A/G]TGGAAACATC	S	A	G	L	L
				necrosis factor
				receptor super-
				family, member 11b
				(osteoprotegerin)
G739u2	WIAF-11874	U94332	1244	TNFRSP11B, tumor	GTATCACAAG[T/C]TATTTTTAGA	S	T	C	L	L
				necrosis factor
				receptor-super-
				family, member 11b
				(osteoprotegerin)
G743u1	WIAF-13402	HT847	1669	PTHR1, parathyroid	CCCTGGAGAC[C/A]CTCGAGACCA	S	C	A	T	T
				hormone receptor 1
G747u1	WIAF-12414	J03040	123	SPARC, secreted	CTCAGCAAGA[A/G]GCCCTGCCTG	S	A	G	E	E
				protein, acidic,
				cysteine-rich
				(osteonectin)
G748u1	WIAF-12628	HT0157	117	VDR, vitamin D	CCTTCAGGGA[T/C]GGAGGCAATG	M	T	C	M	T
				(1,25-dihydroxy-
				vitamin D3)
				receptor
G748u2	WIAF-12629	HT0157	1171	VDR, vitamin D	CCGCGCTGAT[T/C]GAGGCCATCC	S	T	C	I	I
				(1,25-dihydroxy-
				vitamin D3)
				receptor
G748u3	WIAF-12640	HT0157	172	VDR, vitamin D	TTGACCGGAA[C/T]GTGCCCCGGA	S	C	T	N	N
				(1,25-dihydroxy-
				vitamin D3)
				receptor
G749u1	WIAF-11862	HT3734	679	osteopontin, alt.	ATCACCTCAC[A/T]CATGGAAAGC	M	A	T	H	L
				transcript 1
G749u2	WIAF-11875	HT3734	386	osteopontin, alt.	AAGATGATGA[A/G]GACCATGTGG	S	A	G	D	D
				transcript 1
G749u3	WIAF-11876	HT3734	419	osteopontin, alt.	CCATTGACTC[C/A]AACCACTCTC	S	G	A	S	S
				transcript 1
G749a4	WIAF-12084	HT3734	171	osteopontin, alt.	TAAACAGGCT[G/A]ATTCTCGAAC	M	G	A	D	N
				transcript 1
G749u5	WIAF-13387	HT3734	738	osteopontin, alt.	CCAGGACCTG[A/C]ACGCGCCTTC	M	A	C	N	H
				transcript 1
G749u6	WIAF-13388	HT3734	716	osteopontin, alt.	CATACAAGGC[C/A]ATCCCCGTTC	S	C	A	A	A
				transcript 1
G751u1	WIAF-12631	HT5036	410	ADM,	GACAGCAGTC[C/G]GGATGCCGCC	M	C	G	P	R
				adrenomedullin
G752u1	WIAF-11843	HT1782	1405	CHGA, chromogranin	CGGCCATTGA[A/G]GCAGAGCTGG	S	A	G	E	E
				A (parathyroid
				secretory protein
				1)
G752u2	WIAF-11873	HT1782	1187	CHGA, chromogranin	GGACAACCCG[C/A]ACAGTTCCAT	M	G	A	D	N
				A (parathyroid
				secretory protein
				1)
G754a1	WIAF-13382	K02043	663	NPPA, natriuretic	GTACAATGCC[C/A]TGTCCAACGC	M	G	A	V	M
				peptide precursor A
G756u1	WIAF-12395	HT3508	2086	SCNN1A, sodium	CAGTTCCTCC[A/G]CCTGTCCTCT	?	A	G	T	A
				channel, non-
				voltage-gated 1
				alpha
G757u1	WIAF-12420	HT28563	797	SCNN1B, sodium	CCTGCAGGCC[A/C]CCAACATCTT	M	A	C	T	P
				channel, non-
				voltage-gated 1,
				beta (Liddle
				syndrome)
G757u2	WIAF-12421	HT28563	1006	SCNN1B, sodium
				channel, non-
				voltage-gated 1,
				beta (Liddle
				syndrome)
G757u3	WIAF-12430	HT28563	1768	SCNN1B, sodium	TCATCGACTT[T/C]GTGTGGATCA	S	T	C	F	F
				channel, non-
				voltage-gated 1,
				beta (Liddle
				syndrome)
G757u4	WIAF-12494	HT28563	662	SCNN1B, sodium	AAGCAGCTCA[G/C]CATCAGAAAA	M	G	C	A	P
				channel, non-
				voltage-gated 1,
				beta (Liddle
				syndrome)
G757u5	WIAF-12506	HT28563	1091	SCNN1B, sodium	GATGCTTCAC[G/C]AGCAGAGCTC	M	G	C	E	Q
				channel, non-
				voltage-gated 1,
				beta (Liddle
				syndrome)
G757u6	WIAF-12507	HT28563	1452	SCNN1B, sodium	ACCTGCATTC[C/T]CATCTGCAAG	M	G	T	G	V
				channel, non-
				voltage-gated 1,
				beta (Liddle
				syndrome)
G758u1	WIAF-12621	HT27856	415	SCNN1D, sodium	CGGGAACCCA[C/T]GTCGGCCGAG	M	C	T	R	C
				channel, non-
				voltage-gated 1,
				delta
G758u2	WIAF-12632	HT27856	325	SCNN1D, sodium	CCTCTTTGAG[C/T]GTCACTGCCA	M	C	T	R	C
				channel, non-
				voltage-gated 1,
				delta
G758u3	WIAF-12634	HT27856	879	SCNN1D, sodium	ATGGCGTCTG[C/A]ACAGCTCAGC	N	G	A	W	*
				channel, non-
				voltage-gated 1,
				delta
G758u4	WIAF-12635	HT27856	1138	SCNN1D, sodium	CGTGGAGGTG[G/C]AGCTCCTACA	M	G	C	E	Q
				channel, non-
				voltage-gated 1,
				delta
G762u1	WIAF-12622	HT27531	1850	NPR3, natriuretic	TAGGACCTGG[C/T]TTGCTAATGG	S	C	T	G	G
				peptide receptor
				C/guanylate cyclase
				C (atrionatriuretic
				peptide receptor C)
G762u2	WIAF-12623	HT27531	1926	NPR3, natriuretic	AGAAGAAAGT[A/G]ACCTTGGAAA	M	A	G	N	D
				peptide receptor
				C/guanylate cyclase
				C (atrionatriuretic
				peptide receptor C)
				C)
G762u3	WIAF-12624	HT27531	1791	NPR3, natriuretic	CAAATCATCA[G/T]GTGGCCTAGA	M	G	T	G	C
				peptide receptor
				C/guanylate cyclase
				C (atrionatriuretic
				peptide receptor
G762u4	WIAF-12636	HT27531	1963	NPR3, natriuretic	GAAGATTCCA[T/C]CAGATCCCAT	M	T	C	I	T
				peptide receptor
				C/guanylate cyclase
				C (atrionatriuretic
				peptide receptor
				C)
G763u1	WIAF-12659	HT3183	1633	NPR2, natriuretic	CTGGGCCCTT[C/T]CCTGATGAAC	M	C	T	S	F
				peptide receptor
				B/guanylate cyclase
				B (atrionatriuretic
				peptide receptor
				B)
G763u2	WIAF-12678	HT3183	668	NPR2, natriuretic	TGCCATCACT[T/C]CTGCTGTTGG	S	T	C	L	L
				peptide receptor
				B/guanylate cyclase
				B (atrionatriuretic
				peptide receptor
				B)
G763u3	WIAF-12684	HT3183	2354	NPR2, natriuretic	TGTTTGAACT[C/T]AAACATATGA	S	C	T	L	L
				peptide receptor
				B/guanylate cyclase
				B (atrionatriuretic
				peptide receptor
				B)
G764u1	WIAF-12698	HT1221	3021	NPR1, natriuretic	CCCCGTTACT[C/T]TCTCTTTGGG	M	G	T	C	F
				peptide receptor
				A/guanylate cyclase
				A (atrionatriuretic
				peptide receptor
				A)
G764u2	WIAF-12706	HT1221	588	NPR1, natriuretic	GAGCGCCAAG[C/T]GCTCATGCTC	M	C	T	A	V
				peptide receptor
				A/guanylate cyclase
				A (atrionatriuretic
				peptide receptor
				A)
G764u3	WIAF-12709	HT1221	1897	NPR1, natriuretic	GTCCCCGTGG[G/A]AGCCTGCAGG	S	G	A	G	G
				peptide receptor
				A/guanylate cyclase
				A (atrionatriuretic
				peptide receptor
				A)
G765u1	WIAF-10012	HT2456	604	DCP1, dipeptidyl	GCTGGCACAA[A/G]GCTGCGGGCA	S	A	G	N	N
				carboxypeptidase 1
				(angiotensin I
				converting enzyme)
G765u2	WIAF-10014	HT2456	2350	DCP1, dipeptidyl	TGATGGCCAC[A/G]TCCCGCAAAT	S	A	G	T	T
				carboxypeptidase 1
				(angiotensin I
				converting enzyme)
G765u3	WIAF-10025	HT2456	1688	DCP1, dipeptidyl	CCCACTGCAC[C/A]AGTGTCACAT	M	C	A	Q	K
				carboxypeptidase 1
				(angiotensin I
				converting enzyme)
G765u4	WIAF-10027	HT2456	3220	DCP1, dipeptidyl	TCCCCTTCAG[C/T]TACCTCGTCG	S	C	T	S	S
				carboxypeptidase 1
				(angiotensin I
				converting enzyme)
G765u5	WIAF-10028	HT2456	3409	DCP1, dipeptidyl	TCAGGTACTT[T/C]GTCAGCTTCA	S	T	C	F	F
				carboxypeptidase 1
				(angiotensin I
				converting enzyme)
G765u6	WIAF-10040	HT2456	775	DCP1, dipeptidyl	AGCCCCTCTA[C/T]CTGAACCTCC	S	C	T	Y	Y
				carboxypeptidase 1
				(angiotensin I
				converting enzyme)
G772u1	WIAF-12626	HT2121	1064	AVPR2, arginine	TCAGCAGCAC[C/T]GTGTCCTCAG	S	C	T	S	S
				vasopressin
				receptor 2
				(nephrogenic
				diabetes
				insipidus)
G772u2	WIAF-12627	HT2121	998	AVPR2, arginine	CCTTTGTGCT[A/G]CTCATGTTGC	S	A	G	L	L
				vasopressin
				receptor 2
				(nephrogenic
				diabetes
				insipidus)
G773u1	WIAF-12644	HT2141	163	SLC6A6, solute	CTAGCAAGAT[C/T]GACTTTGTGC	S	C	T	I	I
				carrier family 6
				(neurotransmitter
				transporter,
				taurine), member 6
G773u2	WIAF-12645	HT2141	445	SLC6A6, solute	TCGTCATCCT[G/C]GCCTGGGCCA	S	G	C	L	L
				carrier family 6
				(neurotransmitter
				transporter,
				taurine), member 6
G773u3	WIAF-12665	HT2141	289	SLC6A6, solute	TCTTTGGGAG[C/T]GGCCTGCCTG	S	C	T	S	S
				carrier family 6
				(neurotranemitter
				transporter,
				taurine), member 6
G773u4	WIAF-12666	HT2141	382	SLC6A6, solute	CCTTGTTCTC[T/C]GGTATCGGCT	S	T	C	S	S
				carrier family 6
				(neurotransmitter
				transporter,
				taurine), member 6
G776u1	WIAF-11857	U66088	1457	SLC6A6, solute	TAGAACACCT[C/T]ATCAAACCTC	S	C	T	L	L
				carrier family 5
				(sodium iodide
				symporter), member
				5
G776u2	WIAF-11871	U66088	2039	SLC5A5, solute	GATTGTTGTG[G/C]TGGGACCTCG	M	G	C	W	C
				carrier family 5
				(sodium iodide
				symporter), member
				5
G776u3	WIAF-13398	U66088	1379	SLC5A5, solute	GGCTTTTCCT[G/A]GCCTGTGCTT	S	G	A	L	L
				carrier family 5
				(sodium iodide
				symporter), member
				5
G777u1	WIAF-12646	HT27843	4348	SMRT	ATACAATATC[A/G]GCCACCCTGG	M	A	G	S	G
G777u2	WIAF-12654	HT27843	2031	SMRT	CTGAGCTGGG[T/C]AACCCGCGCC	S	T	C	G	G
G777u3	WIAF-12655	HT27643	2052	SMRT	ACACCCCCCT[C/A]ACCTATCACC	S	G	A	L	L
G777u4	WIAF-12675	HT27843	2205	SMRT	CTCGTGACAT[C/T]GCCAAGTCCC	S	C	T	I	I
G778u1	WIAF-14093	HT1449	8212	TG, thyroglobulin	ATCTCCTCTC[T/C]GAACACATCT	M	T	C	L	P
G778u2	WIAF-14111	HT1449	6033	TG, thyroglobulin	ATGTCAACGA[C/T]CGTGCGATGC	M	C	T	R	W
G778u3	WIAF-14112	HT1449	6894	TG, thyroglobulin	GTATCTCAAT[G/T]TGTTCATCCC	M	G	T	V	L
G778u4	WIAF-14125	HT1449	2375	TG, thyroglobulin	ATGGCCCTCC[T/C]GAGCACCTCT	S	T	C	P	P
G778u5	WIAF-14136	HT1449	1931	TG, thyroglobulin	ACCATCTCCA[A/C]TCCTTTTCCC	S	A	G	Q	Q
G783u1	WIAF-12649	X97674	4008	H. sapiens mRNA for	CTACTGGTAT[G/C]CCAGCAACTA	M	G	C	M	I
				transcriptional
				intermediary
				factor 2.
G783u2	WIAF-12658	X97674	2566	H. sapiens mRNA for	GCCTGCCACT[G/A]AGCTGCACAA	M	G	A	E	K
				transcriptional
				intermediary
				factor 2.
G783u3	WIAF-12671	X97674	3828	H. sapiens mRNA for	CTCTGAGCCC[T/C]GGACTACCAA	S	T	C	P	P
				transcriptional
				intermediary
				factor 2.
G785u1	WIAF-13385	HT1291	386	TTR, transthyretin	CCAACCACTC[C/T]GCCCCCCGCC	S	C	T	S	S
				(prealbumin,
				amyloidosis type I)
G787u1	WIAF-12652	HT27477	468	TRIP15: thyroid	GAAAATTATA[T/C]TTAGAACGAG	S	T	C	Y	Y
				receptor
				interacting
				protein 15
G792u1	WIAF-12661	HT27476	265	thyroid receptor	CAGCTGGAAC[G/A]TGAACAGGGC	M	G	A	V	M
				interactor 14
G793u1	WIAF-12643	HT5152	458	thyroid receptor	GGAACCTTTT[C/G]AAAGAATGTT	N	C	G	S	*
				interactor 8
G794u1	WIAF-12664	HT5136	1110	PSMC5, proteasome	GCGTGTCCAC[G/A]GAACCTGGCA	S	G	A	T	T
				(prosome, macro-
				pain) 26S subunit,
				ATPase, 5
G797u1	WIAF-11847	HT3919	140	glutamate receptor	CTCACGGAGG[A/G]TTCCCCAACA	S	A	G	G	G
				3, flip isoform
G797u2	WIAF-11848	HT3919	759	glutamate receptor	GGTTGTGATC[C/T]TAGGGAAACA	S	C	T	L	L
				3, flip isoform
G797u3	WIAF-11849	HT3919	1253	glutamate receptor	GCTACTCCAA[C/T]GACTATGAAA	S	C	T	N	N
				3, flip isoform
G797u4	WIAF-11850	HT3919	1770	glutamate receptor	TCTTTTCCTA[C/A]TCAGCACGTT	M	G	A	V	I
				3, flip isoform
G797u5	WIAF-13404	HT3919	2711	glutamate receptor	GCTACAACGT[G/A]TATGGAACAG	S	G	A	V	V
				3, flip isoform
G797u6	WIAF-13405	HT3919	2376	glutamate receptor	CTCAGCATTA[G/A]GAACGCCTGT	M	G	A	G	R
				3, flip isoform
G798u1	WIAF-11868	X77748	2655	GRM3, glutamate	TGCAGACGAC[A/G]ACCATGTGCA	S	A	G	T	T
				receptor, metabo-
				tropic 3
G798u2	WIAF-11879	X77748	2771	GRM3, glutamate	CACAGACTCC[A/G]CCTCAACAGG	M	A	G	H	R
				receptor,
				metabotropic 3
G798a3	WIAF-12085	X77748	2699	GRM3, glutamate	GTGGTCTTGG[G/C]CTGTTTGTTT	M	G	C	G	A
				receptor,
				metabotropic 3
G798a4	WIAF-12086	X77748	2738	GRM3, glutamate	ATCCTGTTTC[A/G]ACCCCAGAAG	M	A	G	Q	R
				receptor,
				metabotropic 3
G798a5	WIAF-12087	X77748	2072	GRM3, glutamate	ACACCCTTGG[T/C]CAAAGCATCG	M	T	C	V	A
				receptor,
				metabotropic 3
G798a6	WIAF-12088	X77748	2235	GRM3, glutamate	CCCTGCTCAC[C/TI AAGACAAACT	S	C	T	T	T
				receptor,
				metabotropic 3
G798u7	WIAF-13391	X77748	1131	GRM3, glutamate	GCGCCAATGC[C/T]TCCTTCACCT	S	C	T	A	A
				receptor,
				metabotropic 3
G799u1	WIAF-11880	M81883	2000	GAD1, glutamate	CAACAAATGC[C/T]TGGAACTGGC	S	C	T	L	L
				decarboxylase 1
				(brain, 67 kD)
G799u2	WIAF-11881	M81883	1822	GAD1, glutamate	AGGGTATACT[C/T]CAAGGATCCA	S	C	T	L	L
				decarboxylase 1
				(brain, 67 kD)
G799u3	WIAF-13392	M81883	661	GAD1, glutamate	GCGTGGCCCA[T/C]GGATGCACCA	S	T	C	H	H
				decarboxylase 1
				(brain, 67 kD)
G799u4	WIAF-13393	M81883	556	GAD1, glutamate	AGCTGATGGC[G/A]TCTTCGACCC	S	G	A	A	A
				decarboxylase 1
				(brain, 67 kD)
G799u5	WIAF-13410	M81883	1229	GAD1, glutamate	CCTCATGGAA[C/T]AAATAACACT	N	C	T	Q	*
				decarboxylase 1
				(brain, 67 kD)
G801u1	WIAF-13403	D49394	1596	HTR3, 5-hydroxy-	TTTACCTGCT[A/G]GCGGTGCTGG	S	A	G	L	L
				tryptamine
				(serotonin)
				receptor 3
G803a1	WIAF-13118	U66406	1446	EFNB3, ephrin-B3	CTGGGCCTGG[G/A]GGGTGGAGGT	M	G	A	G	E
G804u1	WIAF-11887	Z26653	7237	LAMA2, laminin,	TCACTGATGG[G/T]CACATAAAAG	S	G	T	G	G
				alpha 2 (merosin,
				congenital muscular
				dystrophy)
G804u2	WIAF-11901	Z26653	9351	LAMA2, laminin,	GCAAGCCACT[G/C]GAGGTTAATT	M	G	C	W	S
				alpha 2 (merosin,
				congenital muscular
				dystrophy)
G804u3	WIAF-11924	Z26653	8740	LAMA2, laminin,	ACACTACCCG[A/G]AGAATTGGTC	S	A	G	R	R
				alpha 2 (merosin,
				congenital muscular
				dystrophy)
G804u4	WIAF-11943	Z26653	8577	LAMA2, laminin,	ACCAAAATCA[A/G]TGATGGCCAG	M	A	G	N	S
				alpha 2 (merosin,
				congenital muscular
				dystrophy)
G804a5	WIAF-12089	Z26653	3372	LAMA2, laminin,	CTCTGTGACT[G/A]CTTCCTCCCT	M	G	A	C	Y
				alpha 2 (merosin,
				congenital muscular
				dystrophy)
G804a6	WIAF-13227	Z26653	7047	LAMA2, laminin,	GTCAGTCCTC[A/G]GGTGGAAGAT	M	A	g	Q	R
				alpha 2 (nerosin,
				congenital muscular
				dystrophy)
G804u7	WIAF-13437	Z26653	6791	LAMA2, laminin,	TGTGAGAGCC[C/T]TGGATGGACC	S	C	T	L	L
				alpha 2 (merosin,
				congenital muscular
				dystrophy)
G805u1	WIAF-13416	U14755	799	LHX1, LIM	AAGTAACAGC[A/G]GTGTTGCCAA	M	A	G	S	G
				homeobox protein 1
G805u2	WIAF-13417	U14755	743	LHX1, LIM	GGCGAGGAAC[T/C]CTACATCATC	M	T	C	L	P
				homeobox protein 1
G805u3	WIAF-13428	U14755	639	LHX1, LIM	GCCGTCAGGG[C/A]ATCTCCCCTA	S	C	A	G	G
				homeobox protein 1
G806u1	WIAF-11886	AF026547	2656	CSPG3, chondroitin	TTGGAGTTCC[A/G]GCCATGTCTA	S	A	G	P	P
				sulfate proteo-
				glycan 3
				(neurocan)
G606u2	WIAF-11895	AF026547	529	CSPG3, chondroitin	TGACCTTCGC[T/C]GAGGCCCAGG	S	T	C	A	A
				sulfate proteo-
				glycan 3
				(neurocan)
G806u3	WIAF-11896	AF026547	477	CSPG3, chondroitin	CAGGTGACAG[G/A]TGTTGTGTTC	M	G	A	G	D
				sulfate proteo-
				glycan 3
				(neurocan)
G806u4	WIAF-11917	AF026547	89	CSPG3, chondroitin	ACAGGATATC[A/G]CCGATGCCAG	M	A	G	T	A
				sulfate proteo-
				glycan 3
				(neurocan)
G806u5	WIAF-11918	AF026547	213	CSPG3, chondroitin	AGCGCAGCCC[G/C]AGATCCCCCT	M	G	C	R	P
				sulfate proteo-
				glycan 3
				(neurocan)
G806u6	WIAF-11929	AF026547	769	CSPG3, chondroitin	GCTTTGCCCG[G/A]GAGCTGGGGG	S	G	A	R	R
				sulfate proteo-
				glycan 3
				(neurocan)
G806u7	WIAF-11931	AF026547	3148	CSPG3, chondroitin	ACATTGATGA[C/T]TGCCTCTGCA	S	C	T	D	D
				sulfate proteo-
				glycan 3
				(neurocan)
G806u8	WIAF-11949	AF026547	209	CSPG3, chondroitin	GCCAAGCGCA[G/A]CCCGAGATGC	M	G	A	A	T
				sulfate proteo-
				glycan 3
				(neurocan)
G806a9	WIAF-13114	AF026547	3430	CSPG3, chondroitin	ATGAAAACAC[G/A]TGGATCGGCC	S	G	A	T	T
				sulfate proteo-
				glycan 3
				(neurocan)
G806u10	WIAF-13420	AF026547	2113	CSPG3, chondroitin	CCAGGGCAGA[C/G]TTCAGAGAAA	M	C	G	D	S
				sulfate proteo-
				glycan 3
				(neurocan)
C806u11	WIAF-13431	AF026547	94	CSPG3, chondroitin	ATATCACCGA[T/C]CCCACCCAAA	M	T	C	P	E
				sulfate proteo-
				glycan 3
				(neurocan)
G806u12	WIAF-13432	AF026547	275	CSPG3, chondroitin	ACAGGACTTC[C/T]CCATCCTGGT	M	C	T	P	S
				sulfate proteo-
				glycan 3
				(neurocan)
G808a1	WIAF-13117	Y13276	177	TLX, tailless	GCATGAGCAA[G/a]CCAGCCCGAT	S	G	a	K	K
				homolog
				(Drosophila)
G810u1	WIAF-11890	X98248	990	SORT1, sortilin 1	ATAACGATAC[C/A]ACAAGAAGGA	S	C	A	T	T
G810u2	WIAF-11891	X98248	1093	SORT1, sortilin 1	GGCAGCAAAT[G/T]ATGACATCGT	M	G	T	D	Y
G810u3	WIAF-11907	X98248	1683	SORT1, sortilin 1	CAGACGAAGG[T/C]CAATGCTGGC	S	T	G	G	G
G810u4	WIAF-11908	X98248	1433	SORT1, sortilin 1	ATCTCCCAGA[A/C]ACTGAATGTT	M	A	C	K	T
G810u5	WIAF-11909	X98248	1354	SORT1, sortilin 1	GAAGCCTGAA[A/G]ACAGTGAATG	M	A	G	N	D
G810u6	WIAF-11910	X98248	2180	SORT1, sortilin 1	TACCGGAAAA[T/A]TCCAGGGGAC	M	T	A	I	N
G810u7	WIAF-11911	X98248	2264	SORT1, sortilin 1	AACTTTTTGA[G/A]TCCGGAAAAA	M	G	A	S	N
G810u8	WIAF-11925	X98248	1993	SORT1, sortilin 1	TCGAGACTAT[G/A]TTGTGACCAA	M	G	A	V	I
G810u9	WIAF-11939	X98248	1351	SORT1, sortilin 1	GAGGAAGCCT[G/C]AAAACAGTGA	M	G	C	E	Q
G810u10	WIAF-11940	X98248	2232	SORT1, sortilin 1	AACTAAAAGA[C/T]TTCAAAAAGA	S	C	T	D	D
G810a11	WIAF-13115	X98248	1769	SORT1, sortilin 1	TCCATCAATA[T/A]CACCATTTGC	M	T	A	I	N
G810a12	WIAF-13116	X98248	1757	SORT1, sortilin 1	CCTGGAGCTA[G/A]GTCCATGAAT	M	G	A	R	K
G811u1	WIAF-11893	HT3676	900	synapsin I, alt,	TGACCAAGAC[G/A]TATGCCACTG	S	G	A	T	T
				transcript 1
G811u2	WIAF-11894	HT3676	758	synapsin I, alt,	ACCTTCTACC[C/T]CAATCACAAA	M	C	T	P	L
				transcript 1
G811u3	WIAF-11927	HT3676	996	synapsin I, alt,	CGTCAGTGTC[A/T]GGGAACTGGA	S	A	T	S	S
				transcript 1
G811u4	WIAF-11928	HT3676	1054	synapsin I, alt,	CATGTCTCAC[A/G]CATACAAGCT	M	A	G	R	G
				transcript 1
G811u5	WIAF-13418	HT3676	249	synapsin I, alt,	TGTCCAACGC[G/A[GTCAAGCAGA	S	G	A	A	A
				transcript 1
G811u6	WIAF-13419	HT3676	432	synapsin I, alt,	TTAAAGTAGA[G/A]CAGGCCGAAT	S	G	A	E	E
				transcript 1
G812u1	WIAF-11898	HT4564	163	STX1A, syntaxin	CCAACCCCCA[T/C]GAGAAGACGA	S	T	C	D	D
				1A (brain)
G812u2	WIAF-11942	HT4564	604	STX1A, syntaxin	TACAGGACAT[C/T]TTCATCGACA	M	G	T	M	I
				1A (brain)
G813u1	WIAF-11934	U72508	939	Human B7 mRNA,	TATGACACAG[G/A]ACACAGGATG	M	G	A	G	E
				complete cds.
G813u2	WIAF-11946	U72508	619	Human B7 mRNA,	GCATCCACAT[G/C]CTCACAGGTC	M	G	C	M	I
				complete cds.
G816u1	WIAF-11897	HT4230	151	HTR2B, 5-hydroxy-	CTAACTGGTC[T/C]GCATTACAGA	S	T	G	S	S
				tryptamine
				(serotonin)
				receptor 2B
G816u2	WIAF-11930	HT4230	189	HTR2B, 5-hydroxy-	GAAATGAAAC[A/G]CATTGTTGAC	M	A	G	Q	R
				tryptamine
				(serotonin)
				receptor 2B
G818u1	WIAF-11902	HT2694	753	TPH, tryptophan	GAGTTTTTCA[C/T]TCCACTCAAT	S	C	T	H	H
				hydroxylase
				(tryptophan
				5-monooxygenase)
G818u2	WIAF-11903	HT2694	775	TPH, tryptophan	TGTGAGACAC[A/G]GTTCACATCC	M	A	G	S	G
				hydroxylase
				(tryptophan
				5-monooxygenase)
G818u3	WIAF-11904	HT2694	1211	TPH, tryptophan	TATAATCCAT[A/C]TACACGCAGT	M	A	C	Y	S
				hydroxylase
				(tryptophan
				5-monooxygenase)
G818u4	WIAF-11905	HT2694	1081	TPH, tryptophan	GATTACCTGC[A/C]AACAGGAATG	M	A	C	K	Q
				hydroxylase
				(tryptophan
				5-monooxygenase)
G818u5	WIAF-11933	HT2694	795	TPH, tryptophan	CCTTCTATAC[C/T]CCAGAGCCAG	S	C	T	T	T
				hydroxylase
				(tryptophan
				5-monooxygenase)
G818u6	WIAF-11935	HT2694	1239	TPH, tryptophan	TCCTGAAAGA[C/T]ACCAAGAGCA	S	C	T	D	D
				hydroxylase
				(tryptophan
				5-monooxygenase)
G822u1	WIAF-11906	HT0207	936	ASMT, acetyl-	CAGACGGAAA[G/T]TGCTCACACC	M	G	T	K	N
				serotonin N-
				methyltransferase
G822u2	WIAF-11919	HT0207	637	ASMT, acetyl-	TGGTGCGACA[C/T]CGATAAAGCT	M	C	T	R	W
				serotonin N-
				methyltransferase
G822u3	WIAF-11936	HT0207	318	ASMT, acetyl-	GAAAAGCTTT[C/T]TATCGAAACA	S	C	T	F	F
				serotonin N-
				methyltransferase
G822u4	WIAF-11937	HT0207	116	ASMT, acetyl-	AATGACTACG[C/T]CAACGGCTTC	M	C	T	A	V
				serotonin N-
				methyltransferase
G822u5	WIAF-11938	HT0207	930	ASMT, acetyl-	ACTGGGCAGA[C/T]GGAAAGTGCT	S	C	T	D	D
				serotonin N-
				methyltransferase
G822u6	WIAF-13427	HT0207	120	ASMT, acetyl-	ACTACGCCAA[C/A]GGCTTCATGG	M	C	A	N	K
				serotonin N-
				methyltransferase
G825u1	WIAF-11888	HT4974	236	ADAR, adenosine	GCTCAGATAC[C/T]AGCAGCCTGG	N	C	T	Q	*
				deaminase, RNA-
				specific
G825u2	WIAF-11900	HT4974	3076	ADAR, adenosine	TCTTTGACAA[A/G]TCCTGCAGCG	S	A	G	K	K
				deaminase, RNA
				specific
G825u3	WIAF-11912	HT4974	2537	ADAR, adenosine	CTTGATTGGG[G/C]AGAACGAGAA	M	G	C	E	Q
				deaminase, RNA-
				specific
G825u4	WIAF-11941	HT4974	3558	ADAR, adenosine	GATGGCTATG[A/G]CCTGGAGATC	M	A	G	D	G
				deaminase, RNA-
				specific
G825a5	WIAF-12090	HT4974	1305	ADAR, adenosine	CCTGAGACCA[A/G]AAGAAACGCA	M	A	G	K	R
				deaminase, RNA-
				specific
G825u6	WIAF-13426	HT4974	3683	ADAR, adenosine	CCGCAGGGAT[C/T]TACTGAGACT	S	C	T	L	L
				deaminase, RNA-
				specific
G826u1	WIAF-12554	X99383	2109	ADARB1, adenosine	AGATTACCAA[A/G]CCCAACGTGT	S	A	G	K	K
				deaminase, RNA-
				specific, B1
				(homolog of rat
				RED1)
G826u2	WIAF-12566	X99383	1698	ADARB1, adenosine	TGTCCTCCAG[T/G]GACAAGATTG	M	T	G	S	R
				deaminase, RNA-
				specific, B1
				(homolog of rat
				RED1)
G829u1	WIAF-13735	U49262	1404	DVL3, dishevelled 3	GGGTTGGAGG[T/C]CCGTGACTGC	M	T	C	V	A
				(homologous to
				Drosophila dsh)
G83u1	WIAF-10449	HT1576	1338	DNMT1, DNA	ATGATGACCC[G/A]TCTCTTGAAG	S	G	A	P	P
				(cytosine-5-)-
				methyltransferase 1
G83u2	WIAF-10450	HT1576	1871	DNMT1, DNA	AAGCTGGTCT[A/C]CCAGATCTTC	M	A	G	Y	C
				(cytosine-5-)-
				methyltransferase 1
G83u3	WIAF-10468	HT1576	928	DNMT1, DNA	AAATCCACAG[A/G]TTTCTGATGA	M	A	G	I	V
				(cytosine-5-)-
				methyltransferase 1
G83u4	WIAF-10469	HT1576	1562	DNMT1, DNA	AATTCCGACT[C/T]CACCTATGAG	M	C	T	S	L
				(cytosine-5-)-
				methyltransferase 1
G83u5	WIAF-10471	HT1576	2424	DNMT1, DNA	GGGCCACGTC[G/A]GACCCTCTGC	S	G	A	S	S
				(cytosine-5-)-
				methyltransferase 1
G83u6	WIAF-10473	HT1576	3790	DNMT1, DNA	GTTCTTCCTC[C/T]TGGACAATGT	S	C	T	L	L
				(cytosine-5-)-
				methyltransferase 1
G83u7	WIAF-10486	HT1576	1581	DNMT1, DNA	AGGACCTGAT[C/A]AACAAGATCG	S	C	A	I	I
				(cytosine-5-)-
				methyltransferase 1
G832u1	WIAF-12577	L13387	1129	PAFAH1B1, platelet-	AGACATTCAC[A/T]GGACACAGAG	S	A	T	T	T
				activating factor
				acetylhydrolase,
				isoform Ib, alpha
				subunit (45 kD)
G835u1	WIAF-12555	U38276	1311	SEMA3F, sema	CCTCTGGCTC[C/A]GTGTTCCGAG	S	C	A	S	S
				domain, immuno-
				globulin domain
				(Ig), short
				basic domain,
				secreted, 3F
G835u2	WIAF-12556	U38276	1229	SEMA3F, sema	ACTCACTTTG[A/T]TGACCTCCAG	M	A	T	D	V
				domain, immuno-
				globulin domain
				(Ig), short
				basic domain,
				secreted, 3F
G835u3	WIAF-12557	U38276	1473	SEMA3F, sema	GAACCTTCAC[G/A]CCATCTATGA	S	G	A	T	T
				domain, immuno-
				globulin domain
				(Ig), short
				basic domain,
				secreted, 3F
G835a4	WIAF-13138	U38276	1726	SEMA3F, sema	TGACCACCAC[A/T]TCGACCAGCT	M	A	T	M	L
				domain, immuno-
				globulin domain
				(Ig), short
				basic domain,
				secreted, 3F
G836u1	WIAF-12592	U28369	1056	SEMA3B, sema	AACGACGTGC[G/A]CGGCCAGCGC	M	G	A	G	D
				domain, immuno-
				globulin domain
				(Ig), short
				basic domain,
				secreted, 3B
G836u2	WIAF-12609	U28369	1479	SEMA3B, sema	GTCCTCCCCA[C/T]TGGGGGGCGC	M	C	T	T	I
				domain, immuno-
				globulin domain
				(Ig), short
				basic domain,
				secreted, 3B
G838u1	WIAF-12590	U72671	1107	ICAM5, inter-	CGCAGCTGGG[A/G]CCCAAGCTCT	M	A	G	T	A
				cellular adhesion
				molecule 5,
				telencephalin
G838u2	WIAF-12591	U72671	966	ICAM5, inter-	CAGGCAGCTG[A/G]TCTGCAACGT	M	A	G	I	V
				cellular adhesion
				molecule 5,
				telencephalin
G840a1	WIAF-12109	HT961	2232	SOS1, son of seven-	CTCAGGCAAA[T/C]GGACTAAGCC	S	T	C	N	N
				less (Drosophila)
				homolog 1
G840a2	WIAF-12110	HT961	2404	SOS1, son of seven-	ACCGTCTGAA[C/G]TTGTAGGGAG	M	C	G	L	V
				less (Drosophila)
				homolog 1
G840u3	WIAF-12213	HT961	3813	SOS1, son of seven-	CAAGGGTACC[G/A]CGTCGATGCT	S	G	A	P	P
				less (Drosophila)
				homolog 1
G841u1	WIAF-12153	HT97420	1372	SMOH, smoothened	TTTTGGCTTC[C/G]TGGCCTTTGG	M	C	G	L	V
				(Drosophila)
				homolog
G841u2	WIAF-12179	HT97420	858	SMOH, smoothened	CCCAGTTCAT[G/T]GATCCTGCCC	M	G	T	M	I
				(Drosophila)
				homolog
G841u3	WIAF-12185	HT97420	1164	SMOH, smoothened	CTCTGAGTGG[G/C]ATTTGTTTTG	S	C	G	G	G
				(Drosophila)
				homolog
G847u1	WIAF-12588	L41939	2019	EPHB2, EphB2	GGTCTGCAGT[G/T]GCCACCTGAA	M	G	T	G	C
G847u2	WIAF-12596	L41939	1806	EPHB2, EphB2	GTGTAACAGA[A/C]GACCGGCCTT	S	A	C	R	R
G847u3	WIAF-12613	L41939	2885	EPHB2, EphB2	AGGCCATCAA[G/C]ATGGGGCAGT	M	G	C	K	N
G848u1	WIAF-12685	L40636	2484	EPHB1, EphB1	GTCAACAGTA[A/C]CCTGGTCTGC	M	A	G	N	S
G848u2	WIAF-12690	L40636	2020	EPHB1, EphB1	CCTTCACTTA[T/C]GAGGATCCCA	S	T	C	Y	Y
G849u1	WIAF-11920	D83492	1544	EPHB6, EphB6	ACCTGTGTGG[C/T]TCATCCACAC	M	C	T	A	V
G849u2	WIAF-11921	D83492	3301	EPHB6, EphB6	CTTTGGGATA[C/T]TCATGTGGCA	M	C	T	L	F
G849u3	WIAF-13412	D83492	1139	EPHB6, EphB6	GAGACCTTCA[C/T]CCTTTACTAC	M	C	T	T	I
G849u4	WIAF-13413	D83492	1895	EPHB6, EphH6	TTTGAGGTGC[A/C]AGGCTCAGCA	M	A	C	Q	P
G849u5	WIAF-13414	D83492	2338	EPHB6, EphB6	CTATGACCAG[G/A]CAGAAGACGA	M	G	A	A	T
G849u6	WIAF-13415	D83492	2567	EPHB6, EphB6	GGGGCTTTGG[G/C]CTTCCTCCTG	M	C	G	A	G
G849u7	WIAF-13422	D83492	2860	EPHB6, EphB6	GGCCATCCAG[G/A]CCCTCTGGGC	M	G	A	A	T
G849u8	WIAF-13423	D83492	2782	EPHB6, EphB6	GGAGGTCATT[G/C]GGACAGGCTC	M	A	C	G	R
G849u9	WIAF-13424	D83492	3038	EPHB6, EphB6	TTCCTCAGGC[A/C]GCGGGAGGGC	M	A	G	Q	R
G849u10	WIAF-13425	D83492	3637	EPHB6, EphB6	AGCCATTGGA[C/T]TGGAGTGCTA	S	C	T	L	L
G856u1	WIAF-12625	D45906	1323	LIMK2, LIM domain	AGCTCAACCT[G/C]CTGACAGAGT	S	G	C	L	L
				kinase 2
G858u1	WIAF-12630	U65019	864	MADH2, MAD (mothers	TTTGGTGTTC[G/A]ATAGCATATT	S	G	A	S	S
				against decapenta-
				plegic, Drosophila)
				homolog 2
G86u1	WIAF-10437	HT1701	263	RAD51, RAD51	TGAAGCAAAT[G/C]CAGATACTTC	M	G	C	A	P
				(S. cerevisiae)
				homolog (E coli
				RecA homolog)
G86u2	WIAF-10465	HT1701	861	RAD51, RAD51	GCATCAGCCA[T/C]GATGGTAGAA	M	T	C	M	T
				(S. cerevisiae)
				homolog (E coil
				RecA homolog)
G86u3	WIAF-10466	HT1701	924	RAD51, RAD51	TACAGAACAC[A/G]CTACTCGGGT	M	A	G	D	G
				(S. cerevisiae)
				homolog (E coli
				RecA homolog)
G864a1	WIAF-13139	X82324	183	POU3F4, POU domain,	CAGCAATCGG[C/t]ATCCCCTCCG	M	C	t	H	Y
				class 3, tran-
				scription factor 4
G866u1	WIAF-12637	HT0101	2576	glutamate receptor	AAATCCCGTA[G/A]TCAATCCAAG	M	G	A	S	N
				(GB:M64752)
G866u2	WIAF-12638	HT0101	1131	glutamate receptor	TAACAGGAAA[C/T]GTGCAGTTTA	S	C	T	N	N
				(GB:M64752)
G869u1	WIAF-13406	HT33620	3627	GRIN2C, glutamate	AGATCAGCAG[G/T]GTACCCCCTC	M	G	T	R	S
				receptor, iono-
				tropic, N-methyl
				D-aspartate 2C
G870u1	WZAF-11889	HT4468	714	SLC1A1, solute	CAGAAGAGTC[C/G]TTCACAGCTG	S	C	G	S	S
				carrier family 1
				(neuronal/
				epithelial high
				affinity glutamate
				transporter, system
				Xag), member 1
G870u2	WIAF-11913	HT4468	314	SLC1A1, solute	CTACAGAAAT[T/A]CTACTTTGCT	M	T	A	F	Y
				carrier family 1
				(neuronal/
				epithelial high
				affinity glutamate
				transporter, system
				Xag), member 1
G870u3	WIAF-11914	HT4468	579	SLC1A1, solute	AAGTCAGTAC[G/A]CTCGATGCCA	S	G	A	T	T
				carrier family 1
				(neuronal/
				epithelial high
				affinity glutamate
				transporter, system
				Xag), member 1
G870u4	WIAF-11922	HT4468	706	SLC1A1, solute	GAACATGACA[G/A]AAGAGTCCTT	M	G	A	E	K
				carrier family 1
				(neuronal/
				epithelial high
				affinity glutamate
				transporter, system
				Xag), member 1
G870u5	WIAF-11923	HT4468	978	SLC1A1, solute	GGAAGATCAT[A/G]GAAGTTGAAG	M	A	G	I	M
				carrier family 1
				(neuronal/
				epithelial high
				affinity glutamate
				transporter, system
				Xag), member 1
G871ul	WIAF-11892	HT3187	1004	SLC1A3, solute	TTCTCTTAAC[G/C]AAGCCATCAT	M	G	C	E	Q
				carrier family 1
				(glial high
				affinity glutamate
				transporter),
				member 3
G871u2	WIAF-11915	HT3187	1154	SLC1A3, solute	TGTTGGCTTA[C/T]TCATTCACGC	M	C	T	L	F
				carrier family 1
				(glial high
				affinity glutamate
				transporter),
				member 3
G871u3	WIAF-11926	HT3187	1412	SLC1A3, solute	GGCTGCCATT[T/G]TCATTGCTCA	M	T	G	F	V
				carrier family 1
				(glial high
				affinity glutamate
				transporter),
				member 3
G871u4	WIAF-11944	HT3187	1217	SLC1A3, solute	AAACCCTTGG[G/A]TTTTTATTCC	M	G	A	V	I
				carrier family 1
				(glial high
				affinity glutamate
				transporter),
				member 3
G872u1	WIAF-13433	HT4077	1271	SLC1A2, solute	CTGTTGGAGC[A/C]ACCATTAACA	S	A	C	A	A
				carrier family 1
				(glial high
				affinity glutamate
				transporter),
				member 2
G879u1	WIAF-11899	HT28317	1273	GRM2, glutamate	GACTTTGTGC[T/C]CAACGTCAAG	M	T	C	L	P
				receptor, metabo-
				tropic 2
G879u2	WIAF-11932	HT28317	2349	GRM2, glutamate	CTTCTATGTC[A/C]CCTCCAGTGA	M	A	G	T	A
				receptor, metabo-
				tropic 2
G879u3	WIAF-13421	HT28317	2186	GRM2, glutamate	ATGCAAGTAT[G/T]TTGGGCTCGC	M	G	T	M	I
				receptor, metabo-
				tropic 2
G879u4	WIAF-13429	HT28317	2567	GRM2, glutamate	CCCAGTTTGT[C/T]CCCACTGTTT	S	C	T	V	V
				receptor, metabo-
				tropic 2
G879u5	WIAF-13436	HT28317	2046	CRM2, glutamate	ACAGGTGGCC[A/G]TCTGCCTGGC	M	A	G	I	V
				receptor, metabo-
				tropic 2
G879u6	WIAF-13438	HT28317	2425	GRM2, glutamate	GTCCTTGGCT[C/T]CCTCTTTGCG	M	G	T	C	F
				receptor, metabo-
				tropic 2
G879u7	WIAF-13439	HT28317	2463	GRM2, glutamate	CCTCTTCCAG[C/T]CGCAGAAGAA	M	C	T	P	S
				receptor, metabo-
				tropic 2
G880u1	WIAF-12164	HT33719	2117	GRM4, glutamate	AGCCCGACCT[T/G]GGCACCTGCT	S	T	G	L	L
				receptor, metabo-
				tropic 4
G880u2	WIAF-12176	HT33719	2427	GRM4, glutamate	GGACCTGTCG[C/T]TCATCTGCCT	M	C	T	L	F
				receptor, metabo-
				tropic 4
G880u3	WIAF-12192	HT33719	2372	GRM4, glutamate	ACCAGCGGAC[A/G]CTCGACCCCC	S	A	G	T	T
				receptor, metabo-
				tropic 4
G883a1	WIAF-13140	HT48863	1408	GRM7, glutamate	ATCGCAAATC[C/a]ACAGGACAGG	N	C	a	C	*
				receptor, metabo-
				tropic 7
G883a2	WIAF-13141	HT48863	2027	GRM7, glutamate	TCCTGTCTTC[C/t]TGGCAATGTT	S	C	t	L	L
				receptor, metabo-
				tropic 7
G883a3	WIAF-13147	HT48863	1813	GRM7, glutamate	TGTGCACACT[A/g]CCATGTAAGC	S	A	g	L	L
				receptor, metabo-
				tropic 7
G883a4	WIAF-13148	HT48863	1536	GRM7, glutamate	TGTGCTGACT[A/t]CCGGGCTCTC	M	A	t	Y	F
				receptor, metabo-
				tropic 7
G883a5	WIAF-13149	HT48863	2473	GRM7, glutamate	AAGCCAGAGG[G/a]GTTCTCAAGT	S	G	a	G	G
				receptor, metabo-
				tropic 7
G883a6	WIAF-13150	HT48863	2434	GRM7, glutamate	TCATAGACTA[C/t]GATGAACACA	S	C	t	Y	Y
				receptor, metabo-
				tropic 7
G884u1	WIAF-11916	U95025	1052	GRM8, glutamate	CGAACTCTTG[C/A]CAATAATCGA	M	C	A	A	D
				receptor,
				metabotropic 8
G884u2	WIAF-11945	U95025	2016	GRM8, glutamate	AAACAAACCG[T/C]ATCCACCGAA	S	T	C	R	R
				receptor, metabo-
				tropic 8
G884u3	WIAF-11946	U95025	1852	GRM8, glutamate	CAGGGCTTCA[G/A]GACGCGAACT	M	G	A	G	R
				receptor, metabo-
				tropic 8
G884u4	WIAF-11947	U95025	2078	GRM8, glutamate	ATTAGTCCAG[C/G]ATCTCAGCTG	M	C	G	A	G
				receptor, metabo-
				tropic 8
G884u5	WIAF-13430	U95025	1897	GRM8, glutamate	TTTTCTCTGT[T/G]ATTCAATCAC	M	T	G	Y	D
				receptor, metabo-
				tropic 8
G884u6	WIAF-13435	U95025	2364	GRM8, glutamate	TTACCATGTA[T/C]ACCACCTGCA	S	T	C	Y	Y
				receptor, metabo-
				tropic 8
G885u1	WIAF-13434	AF002700	1363	GFRA2, GDNF family	AACTCAGGCC[C/A]CAGCACAGCC	M	C	A	P	H
				receptor alpha 2
G886a1	WIAF-13142	U95847	497	GFRA1, GDNF family	GAAGTCCCTC[T/a]ACAACTGCCG	M	T	a	Y	N
				receptor alpha 1
G886a2	WIAF-13143	U95847	1385	GFRA1, GDNF family	GTCTGAGAAT[G/a]AAATTCCCAC	M	G	a	E	K
				receptor alpha 1
G886a3	WIAF-13151	U95847	781	GFRA1, GDNF family	GCGTGTCCAA[T/C]GATGTCTGCA	S	T	c	N	N
				receptor alpha 1
G892u1	WIAF-11956	U12140	798	NTRK2, neuro-	TGGGCAATCC[A/C]TTTACATGCT	S	A	G	P	P
				trophic tyrosine
				kinase, receptor,
				type 2
G892u2	WIAF-11957	U12140	834	NTRK2, neuro-	GGATCAAGAC[T/A]CTCCAACAGC	S	T	A	T	T
				trophic tyrosine
				kinase, receptor,
				type 2
G892u3	WIAF-11958	U12140	956	NTRK2, neuro-	GCAAATCTGG[C/T]CGCACCTAAC	M	C	T	A	V
				trophic tyrosine
				kinase, receptor,
				type 2
G892u4	WIAF-11960	U12140	1738	NTRK2, neuro-	CTCCAAGTTT[G/A]GCATCAAAGG	M	G	A	G	S
				trophic tyrosine
				kinase, receptor,
				type 2
G892u5	WIAF-11962	U12140	2486	NTRK2, neuro-	GTCGGTGGCC[A/C]CACAATGCTG	M	A	G	H	R
				trophic tyrosine
				kinase, receptor,
				type 2
G892u6	WIAF-11965	U12140	1106	NTRK2, neuro-	TCCTTAAGGA[T/C]AACTAACATT	M	T	C	I	T
				trophic tyrosine
				kinase, receptor,
				type 2
G892u7	WIAF-11966	U12140	2085	NTRK2, neuro-	AGGATGCCAG[T/C]GACAATGCAC	S	T	C	S	S
				trophic tyrosine
				kinase, receptor,
				type 2
G892u8	WIAF-11967	U12140	2230	NTRK2, neuro-	GGACCTCAAC[A/C]AGTTCCTCAG	M	A	C	K	Q
				trophic tyrosine
				kinase, receptor,
				type 2
G892u9	WIAF-11968	U12140	2223	NTRK2, neuro-	AGCATGGGGA[C/T]CTCAACAAGT	S	C	T	D	D
				trophic tyrosine
				kinase, receptor,
				type 2
G892u10	WIAF-11992	U12140	1602	NTRK2, neuro-	GTAATCAAAT[C/T]CCTTCCACAG	S	C	T	I	I
				trophic tyrosine
				kinase, receptor,
				type 2
G892u11	WIAF-11998	U12140	1354	NTRK2, neuro-	TACTAAAATA[C/T]ATGTTACCAA	M	C	T	H	Y
				trophic tyrosine
				kinase, receptor,
				type 2
G892u12	WIAF-11999	U12140	1944	NTRK2, neuro-	CATTTGTTCA[G/C]CACATCAAGC	M	G	C	Q	H
				trophic tyrosine
				kinase, receptor,
				type 2
G892u13	WIAF-12000	U12140	2103	NTRK2, neuro-	CACGCAAGGA[C/T]TTCCACCGTG	S	C	T	D	D
				trophic tyrosine
				kinase, receptor,
				type 2
G892u14	WIAF-12001	U12140	1860	NTRK2, neuro-	CTGTCATTAT[T/C]GGAATGACCA	S	T	C	I	I
				trophic tyrosine
				kinase, receptor,
				type 2
G892a15	WIAF-13144	U12140	1868	NTRK2, neuro-	ATTGGAATGA[C/G]CAAGATCCCT	M	C	G	T	S
				trophic tyrosine
				kinase, receptor,
				type 2
G892a16	WIAF-13145	U12140	1903	NTRK2, neuro-	CCAGTACTTT[C/T]GCATCACCAA	M	G	T	G	C
				trophic tyrosine
				kinase, receptor,
				type 2
G892a17	WIAF-13146	U12140	1965	NTRK2, neuro-	GACATAACAT[T/G]GTTCTGAAAA	M	T	G	I	M
				trophic tyrosine
				kinase, receptor,
				type 2
G892u18	WIAF-13442	U12140	958	NTRK2, neuro-	AAATCTGGCC[G/T]CACCTAACCT	M	G	T	A	S
				trophic tyrosine
				kinase, receptor,
				type 2
G892u19	WIAF-13446	U12140	2502	NTRK2, neuro-	TGCTGCCCAT[T/C]CGCTGGATGC	S	T	C	I	I
				trophic tyrosine
				kinase, receptor,
				type 2
G892u20	WIAF-13447	U12140	2317	NTRK2, neuro-	GATGCTGCAT[A/T]TAGCCCAGCA	M	A	T	I	L
				trophic tyrosine
				kinase, receptor,
				type 2
G892u21	WIAF-13448	U12140	2364	NTRK2, neuro-	CGTCCCAGCA[C/A]TTCGTGCACC	M	C	A	H	Q
				trophic tyrosine
				kinase, receptor,
				type 2
G892u22	WIAF-13449	U12140	2507	NTRK2, neuro-	CCCATTCGCT[G/A]GATCCCTCCA	N	G	A	W	*
				trophic tyrosine
				kinase, receptor,
				type 2
G892u23	WIAF-13471	U12140	2389	NTRK2, neuro-	TTTGCCCACC[A/C]CGAACTCCCT	S	A	C	R	R
				trophic tyrosine
				kinase, receptor,
				type 2
G892u24	WIAF-13472	U12140	2416	NTRK2, neuro-	GGAGAACTTG[C/T]TCGTGAAAAT	S	C	T	L	L
				trophic tyrosine
				kinase, receptor,
				type 2
G892u25	WIAF-13474	U12140	359	NTRK2, neuro-	GGGATCTCGT[C/T]CTGGATAAGG	M	C	T	S	F
				trophic tyrosine
				kinase, receptor,
				type 2
G892u26	WIAF-13479	U12140	1044	NTRK2, neuro-	TGTATTGGGA[T/C]GTTGGTAACC	S	T	C	D	D
				trophic tyrosine
				kinase, receptor,
				type 2
G9u1	WIAF-10222	J03826	1130	FDXR, ferredoxin	GGTATAAGAG[C/T]CGCCCTGTCG	S	C	T	S	S
				reductase
G9u2	WIAF-10258	J03826	388	FDXR, ferredoxin	CCGGAGCTGC[A/C]GGAGGCCTAC	M	A	G	Q	R
				reductase
G900u1	WIAF-11970	HT3470	497	STX4A, syntaxin 4A	TGCAATTCAA[T/C]GCACTCCGAA	M	T	C	M	T
				(placental)
G901u1	WIAF-11969	HT27792	758	STX3A, syntaxin 3A	TGCACACAGT[G/A]GACCACGTGG	S	G	A	V	V
G901u2	WIAF-11971	HT27792	317	STX3A, syntaxin 3A	ACGTCCGGAA[C/A]AAACTGAAGA	M	C	A	N	K
G901u3	WIAF-12002	HT27792	611	STX3A, syntaxin 3A	AGCAAGCCCT[C/T]AGTGAGATTG	S	C	T	L	L
G901u4	WIAF-12003	HT27792	909	STX3A, syntaxin 3A	CCTCAATTAA[C/A]ACTCCCCTAA	—	G	A	—	—
G901u5	WIAF-12004	HT27792	163	STX3A, syntaxin 3A	ATTGAGGAAA[C/T]TCGGCTTAAC	M	C	T	T	I
G901a6	WIAF-13152	HT27792	82	STX3A, syntaxin 3A	CAGCTGACAC[A/C]GGATGATGAT	M	A	G	Q	R
G901u7	WIAF-13453	HT27192	828	STX3A, syntaxin 3A	CCGGAAGAAA[T/C]TGATAATTAT	S	T	C	L	L
G901u8	WIAF-13455	HT27792	226	STX3A, syntaxin 3A	TACAGTATCA[T/C]TCTCTCTGCA	M	T	C	I	T
G902u1	WIAF-13454	HT27744	848	STX5A, syntaxin 5A	ACTTCCAGTC[T/A]GTCACCTCCA	S	T	A	S	S
G902u2	WIAF-13456	HT27744	338	STX5A, syntaxin 5A	ATTTCGTGAG[A/G]GCCAAGGGCA	S	A	G	R	R
G905u1	WIAF-12202	HT27789	487	CREBL1, cAMP	TCCAGATCAA[C/T]GTTATCCCCA	S	C	T	N	N
				responsive element
				binding protein-
				like 1
G905u2	WIAF-12219	HT27789	151	CREBL1, cAMP	ATTCTGCCCT[A/T]GATCAAGTGG	S	A	T	L	L
				responsive element
				binding protein-
				like 1
G905u3	WIAF-12230	HT27789	649	CREBL1, cAMP	AGTCCCTGTC[C/G]CCTTCAGGAT	S	C	G	S	S
				responsive element
				binding protein-
				like 1
G906u1	WIAF-12214	HT4372	2127	N-ethylmaleimide-	AAGGGAAGAA[G/A]GTCTGGATAG	S	G	A	K	K
				sensitive factor
G906u2	WIAF-12221	HT4372	514	N-ethylmaleimide-	GGGAGAGCCT[G/A]CGACAGGGAA	M	G	A	A	T
				sensitive factor
G908u1	WIAF-12201	HT3665	98	RAB5A, RAB5A,	GCCCAAATAC[T/G]GGAAATAAAA	S	T	G	T	T
				member RAS
				oncogene family
G91u1	WIAF-10438	HT1848	496	ERCC1, excision	TCGTGCGCAA[C/T]GTGCCCTGGG	S	C	T	N	N
				repair cross-
				complementing
				rodent repair
				deficiency, com-
				plementation group
				1 (includes over-
				lapping antisense
				sequence)
G91u2	WIAF-10439	HT1848	367	ERCC1, excision	CTGGCGCCAC[G/A]TGCCCCACAG	S	C	A	T	T
				repair cross-
				complementing
				rodent repair
				deficiency,
				complementation
				group 1 (includes
				overlapping anti-
				sense sequence)
G914a1	WIAF-13210	HT3672	252	synaptobrevin 1	GCAGTGCTGC[C/A]AAGCTAAAGA	S	G	A	A	A
G915a1	WIAF-12115	D63506	1390	Homo sapiens mRNA	TTACCTTGGT[G/A]TTCCCATTGT	M	G	A	V	I
				for unc-
				18homologue,
				complete cds.
G915u2	WIAF-12293	D63506	685	Homo sapiens mRNA	ACAGCTTGTT[G/A]AAAAAAAGCT	M	G	A	E	K
				for unc-
				18homologue,
				complete cds.
G916a1	WIAF-13209	HT28523	308	Huntingtin	GAGCACTTTT[C/T]GGAGGCCAGC	M	C	T	S	L
				associated protein
				1-like protein
G916a2	WIAF-13211	HT28523	762	Huntingtin	CGGAGGACTT[G/C]GTCCCCCACG	M	G	C	L	F
				associated protein
				1-like protein
G916a3	WIAF-13212	HT28523	560	Huntingtin	GAGCTCAGAA[C/T]GTCTCTAAGG	M	C	T	T	N
				associated protein
				1-like protein
G917u1	WIAF-11972	U79734	1075	HIP1, huntingtin	AGAGCCAGCG[G/A]GTTGTGCTGC	S	G	A	R	R
				interacting
				protein 1
G917u2	WIAF-11973	U79734	1005	HIP1, huntingtin	GACCACTTAA[T/C]TGAGCGACTA	M	T	C	I	T
				interacting
				protein 1
G917u3	WIAF-11977	U79734	1539	HIP1, huntingtin	CTGCAAGGCA[G/A]CCTGGAAACT	M	G	A	S	N
				interacting
				protein 1
G917u4	WIAF-12005	U79734	817	HIP1, huntingtin	TGGTGGTGAT[C/T]CCTGCAGAGG	S	C	T	I	I
				interacting
				protein 1
G917u5	WIAF-12006	U79734	1906	HIP1, huntingtin	GCTGGAGCCA[G/C]TATCTGGCCT	M	G	C	Q	H
				interacting
				protein 1
G917a6	WIAF-13157	U79734	993	HIP1, huntingtin	AAGGATGAGA[A/G]GGACCACTTA	M	A	G	K	R
				interacting
				protein 1
G919u1	WIAF-11974	D30742	707	CAMK4, calcium/	ACTGCGCACC[T/C]GAAATTCTTA	S	T	C	P	P
				calmodulin
				dependent protein
				kinase IV
G919u2	WIAF-11991	D30742	1139	CAMK4, calcium/	AGAGCCACAA[G/A]GCTAGCCGAG	S	G	A	K	K
				calmodulin
				dependent protein
				kinase IV
G919u3	WIAF-12007	D30742	834	CAMK4, calcium/	CATGTTCAGG[A/T]GAATTCTGAA	N	A	T	R	*
				calmodulin
				dependent protein
				kinase IV
G919u4	WIAF-13443	D30742	1088	CAMK4, calcium/	TGGCCTCTTC[C/G]CGCCTGGGAA	S	C	G	S	S
				calmodulin-
				dependent protein
				kinase IV
G920u1	WIAF-11979	X78520	1952	CLCN3, chloride	ATGACATTCC[T/C]GATCGTCCAG	S	T	C	P	P
				channel 3
G920u2	WIAF-11980	X78520	1819	CLCN3, chloride	ATAGCCTTCC[C/T]TAATCCATAC	M	C	T	P	L
				channel 3
G920u3	WIAF-11981	X78520	2094	CLCN3, chloride	CATTGGAGCG[A/C]TCGCAGCGAAG	M	A	G	I	V
				channel 3
G920u4	WIAF-11983	X78520	2822	CLCN3, chloride	ATATTTTCCG[A/G]AAGCTGGGAC	S	A	G	R	R
				channel 3
G920u5	WIAF-11984	X78520	2745	CLCN3, chloride	GCCATTGAAG[C/T]TTCCAAGCAT	M	C	T	L	F
				channel 3
G920u6	WIAF-11987	X78520	2499	CLCN3, chloride	TCCCTTACCT[C/T]TCCTGACACA	M	G	T	V	F
				channel 3
G920u7	WIAF-12008	X78520	1251	CLCN3, chloride	CATCATCACA[G/A]GTTACTTGGC	M	G	A	G	S
				channel 3
G920u8	WIAF-12011	X78520	888	CLCN3, chloride	AGTACTAACA[C/T]TAACACGATT	S	C	T	L	L
				channel 3
G920u9	WIAF-13459	X78520	2804	CLCN3, chloride	CAATCGACAT[T/C]GTCCTCCATA	S	T	C	I	I
				channel 3
G921u1	WIAF-11954	J02908	931	CLU, clusterin	GAGACCTTGA[C/T]CAGGAAATAC	M	C	T	T	I
				(complement lysis
				inhibitor, SP-40,
				40, sulfated glyco-
				protein 2,
				testosterone-
				repressed prostate
				message 2,
				apolipoprotein J)
G921u2	WIAF-11955	J02908	880	CLU, clusterin	CCCTCCCAGG[C/T]TAAGCTCCGG	M	C	T	A	V
				(complement lysis
				inhibitor, SP-40,
				40, sulfated glyco-
				protein 2,
				testosterone-
				repressed prostate
				message 2,
				apolipoprotein J)
G921u3	WIAF-11990	J02908	1051	CLU, clusterin	CTCACCCAAG[G/C]CGAACACCAG	M	G	C	G	A
				(complement lysis
				inhibitor, SP-40,
				40, sulfated glyco-
				protein 2,
				testosterone-
				repressed prostate
				message 2,
				apolipoprotein J)
G921u4	WIAF-13469	J02908	986	CLU, clusterin	TCAACACCTC[C/T]TCCTTCCTGG	S	C	T	S	S
				(complement lysis
				inhibitor, SP-40,
				40, sulfated glyco-
				protein 2,
				testosterone-
				repressed prostate
				message 2,
				apolipoprotein J)
G923u1	WIAF-11993	M19650	1059	Human 2′,3′-cyclic	GAGCTAAGCC[G/A]GGGCAAGCTC	M	G	A	R	Q
				nucleotide 3′-
				phosphodiesterase
				mRNA, complete
				cds.
G923u2	WIAF-11994	M19650	1062	Human 2′,3′-cyclic	CTAAGCCGGG[G/T]CAAGCTCTAT	M	G	T	G	V
				nucleotide 3′-
				phosphodiesterase
				mRNA, complete
				cds.
G923u3	WIAF-13445	M19650	1141	Human 2′,3′-cyclic	TCTTCACGGG[C/A]TACTACGGGA	S	G	A	G	G
				nucleotide 3′-
				phosphodiesterase
				mRNA, complete
				cds.
G925u1	WIAF-11953	L11315	666	CAK, cell adhesion	GGGTCATGAG[T/C]GTCTCTCTGC	S	T	C	S	S
				kinase
G925u2	WIAF-11959	L11315	2562	CAK, cell adhesion	TGCTGCCCAT[C/T]CGCTGGATCC	S	C	T	I	I
				kinase
G925u3	WIAF-11996	L11315	2049	CAK, cell adhesion	AAGATCTCCT[T/C]AGTCTTCATT	S	T	C	V	V
				kinase
G925u4	WIAF-13440	L11315	1601	CAK, cell adhesion	TACCAGGAGC[C/T]CCGGCCTCGT	M	C	T	P	L
				kinase
G925u5	WIAF-13441	L11315	1629	CAK, cell adhesion	CGCCCCACTC[C/T]GCTCCCTGTG	S	C	T	S	S
				kinase
G925u6	WIAF-13451	L11315	2262	CAK, cell adhesion	TGGACAACGG[C/T]GACCTCAACC	S	C	T	G	G
				kinase
G926u1	WIAF-11961	AF018956	577	NRP1, neuropilin 1	TGAAAGCTTT[C/T]ACCTGGACCC	M	G	T	D	Y
G926u2	WIAF-11963	AF018956	1683	NRP1, neuropilin 1	CCACCCGATT[G/C]ATCAGGATCT	M	C	G	F	L
G926u3	WIAF-11975	AF018956	2176	NRP1, neuropilin 1	GACCTTCTGG[T/C]ATCACATGTC	M	T	C	Y	H
G926u4	WIAF-11976	AF018956	2092	NRP1, neuropilin 1	TTCCCAAGCT[G/T]ACGAAAATCA	M	G	T	D	Y
G926a5	WIAF-13158	AF018956	747	NRP1, neuropilin 1	TTTTTTACAC[C/T]GACAGCGCGA	S	C	T	T	T
G926a6	WIAF-13159	AF018956	996	NRP1, neuropilin 1	ACTTGGGCCT[T/C]CTGCGCTTTC	S	T	C	L	L
G926u7	WIAF-13444	AF018956	644	NRP1, neuropilin 1	GAAATCTGGG[A/C]TGGATTCCCT	M	A	C	D	A
G926u8	WIAF-13450	AF018956	1738	NRP1, neuropilin 1	CAGAATGGAG[C/G]TGCTCGGCTG	M	C	C	L	V
G926u9	WIAF-13452	AF018956	537	NRP1, neuropilin 1	TTGTCTTTCC[C/A]CCAAAGATGT	S	C	A	A	A
G926u10	WIAF-13457	AF018956	2197	NRP1, neuropilin 1	TGGCTCCCAC[G/A]TCGGCACACT	M	G	A	V	I
G927u1	WIAF-11978	AF022860	870	NRP2, neuropilin 2	GGATTCCTAA[T/C]GAACAGATCA	S	T	C	N	N
G927u2	WIAF-11982	AF022860	1674	NRP2, neuropilin 2	ATCACACCCC[T/G]GACATCCGAA	S	T	G	P	P
G927u3	WIAF-11985	AF022860	1250	NRP2, neuropilin 2	TGGCACTCAG[C/A]TATCGCCCTC	M	G	A	G	D
G927u4	WIAF-11986	AF022860	1071	NRP2, neuropilin 2	ATGGCTACTA[C/T]GTCAAATCCT	S	C	T	Y	Y
G927u5	WIAF-12009	AF022860	726	NRP2, neuropilin 2	GTTCATCCAC[G/A]GCGATCCTCT	S	G	A	T	T
G927u6	WIAF-12010	AF022860	2522	NRP2, neuropilin 2	GCAACCTCAG[G/T]GTCTGGCGCC	M	G	T	C	V
G927u7	WIAF-12012	AF022860	123	NRP2, neuropilin 2	GCTATATCAC[C/T]TCTCCCCGTT	S	C	T	T	T
G927a8	WIAF-13160	AF022860	2427	NRP2, neuropilin 2	CTTTTCCAGT[G/T]CACATCCCAG	S	C	T	V	V
G927a9	WIAF-13161	AF022860	2430	NRP2, neuropilin 2	TTGCAGTGGA[C/G]ATCCCAGAAA	M	C	G	D	E
G927a10	WIAF-13162	AF022860	2463	NRP2, neuropilin 2	AACCATATCA[A/G]GATCAAATTG	S	A	G	E	E
G927a11	WIAF-13163	AF022860	2473	NRP2, neuropilin 2	AGATGAAATT[G/T]ATCATCAATA	M	G	T	D	Y
G927u12	WIAF-13480	AF022860	724	NRP2, neuropilin 2	TCGTTCATCG[A/T]CGGGGATCCT	M	A	T	T	S
G927u13	WIAF-13481	AF022860	767	NRP2, neuropilin 2	ATGCCCGTGC[C/T]CAAGGATGCC	M	C	T	A	V
G930a1	WIAF-13164	HT2608	609	GABRA2, gamma-	ACAATGGGAA[G/a]AAATCAGTAG	S	G	a	K	K
				aminobutyric acid
				(GASA) A receptor,
				alpha 2
G931a1	WIAF-13153	HT2609	1111	GABRA3, gamma-	ACTGGTTCAT[A/g]GCCCTCTGTT	M	A	g	I	M
				aminobutyric acid
				(GABA) A receptor,
				alpha 3
G931a2	WIAF-13165	HT2609	1448	GABRA3, gamma-	TGTCAGCAAG[G/A]TTCACAAAAT	M	G	A	V	I
				aminobutyric acid
				(GASA) A receptor,
				alpha 3
G932a1	WIAF-13154	HT27773	1077	GABRA4, gamma-	CAAAAGAAAG[A/G]CATCAAACCC	M	A	G	T	A
				aminobutyric acid
				(GABA) A receptor,
				alpha 4
G932a2	WIAF-13155	HT27773	1189	GABRA4, gamma-	AGAACAAATG[C/A]TTTGGTTCAC	M	C	A	A	D
				aminobutyric acid
				(GABA) A receptor,
				alpha 4
G936u1	WIAF-12308	HT3432	1027	GABRB2, gamma-	AATTACGATG[C/T]TTCACCTGCA	M	C	T	A	V
				aminobutyric acid
				(GABA) A receptor,
				beta 2
G936u2	WIAF-12327	HT3432	362	GABRB2, gamma-	AAGGCTATGA[C/T]ATTCGTCTGA	S	C	T	D	D
				aminobutyric acid
				(GABA) A receptor,
				beta 2
G936u3	WIAF-12328	HT3432	571	GABRB2, gamma-	CTCTGGGTG[C/T]TGATACCTAT	M	C	T	P	L
				aminobutyric acid
				(GABA) A receptor,
				beta 2
G939u1	WIAF-12330	HT2236	1219	GABRR2, gamma-	CTGGATGGAA[G/C]CTACAGTGAG	M	G	C	S	T
				aminobutyric acid
				(GABA) receptor,
				rho 2
G939u2	WIAF-12355	HT2236	1003	GABRR2, gamma-	ACCACCATCA[T/C]CACGGGCGTG	M	T	C	I	T
				aminobutyric acid
				(GABA) receptor,
				rho 2
G939u3	WIAF-12356	HT2236	1041	CABRR2, gamma-	CGTCTCCTAC[G/A]TCAAGGCCGT	M	G	A	V	I
				aminobutyric acid
				(GABA) receptor,
				rho 2
G950u1	WIAF-13622	U64871	725	Human putative G	GTCCTGCTCC[A/C]GTTCACCACT	M	A	C	Q	P
				protein-coupled
				receptor (GPR19)
				gene, complete
				cds.
G950u2	WIAF-13624	U64871	443	Human putative G	GATAACAGCA[A/C]GCCACATTTG	M	A	C	K	T
				protein-coupled
				receptor (GPR19)
				gene, complete
				cds.
G950u3	WIAF-13625	U64871	818	Human putative G	CTGGGTAGTG[C/T]AACGTGCAAG	M	C	T	A	V
				protein-coupled
				receptor (GPR19)
				gene, complete
				cds.
G955a1	WIAF-13166	HT3860	5110	calcium channel,	CTGGCCTCTT[T/c]ACCGTGGAGA	S	T	c	F	F
				voltage-gated,
				alpha 1 subunit,
				L type, alt.
				transcript 1
G955a2	WIAF-13167	HT3860	3842	calcium channel,	CTACCCCAAC[C/a]CAGAAACTAC	M	C	a	P	T
				voltage-gated,
				alpha 1 subunit,
				L type, alt.
				transcript 1
G955a3	WIAF-13168	HT3860	5624	calcium channel,	GTGTGCCCCA[G/a]AGTCCGAGCC	M	G	a	E	K
				voltage-gated,
				alpha 1 subunit,
				L type, alt.
				transcript 1
G955a4	WIAF-13169	HT3860	5703	calcium channel,	ATCAGCTTCT[A/g]CATGCTCTGT	M	A	g	Y	C
				voltage-gated,
				alpha 1 subunit,
				L type, alt.
				transcript 1
G955a5	WIAF-13170	HT3860	5809	calcium channel,	ACCACCTGGA[T/c]GAGTTTAAAA	S	T	c	D	D
				voltage-gated,
				alpha 1 subunit,
				L type, alt.
				transcript 1
G955a6	WIAF-13171	HT3860	6616	calcium channel,	CCGGCTCCAA[C/t]GCCAACATCA	S	C	t	N	N
				voltage-gated,
				alpha 1 subunit,
				L type, alt.
				transcript 1
G956u1	WIAF-14187	HT2199	1334	calcium channel,	CTTCACATAG[C/T]CCTTTTGGTA	M	C	T	A	V
				voltage-gated,
				alpha 1D subunit,
				DHP-sensitive
G956u2	WIAF-14188	HT2199	1452	calcium channel,	AAGAGGACCC[A/T]GCTCCATGTG	S	A	T	P	P
				voltage-gated,
				alpha 1D subunit,
				DHP-sensitive
G956u3	WIAF-14189	HT2199	1614	calcium channel,	GCTGGACAGA[C/T]GTGCTCTACT	S	C	T	D	D
				voltage-gated,
				alpha 1D subunit,
				DHP-sensitive
G956u4	WIAF-14190	HT2199	2540	calcium channel,	GGCAAGTTTA[A/T]TTTTGATGAA	M	A	T	N	I
				voltage-gated,
				alpha 1D subunit,
				DHP-sensitive.
G956u5	WIAF-14191	HT2199	3210	calcium channel,	TGCTGACCAC[T/C]GCTCCCCTGG	S	T	C	S	S
				voltage-gatad,
				alpha 1D subunit,
				DHP-sensitive
G956u6	WIAF-14192	HT2199	3326	calcium channel,	TTGAAGATGA[C/T]AACTTTTGGA	M	C	T	T	I
				voltage-gated,
				alpha 1D subunit,
				DHP-sensitive
G956u7	WIAF-14193	HT2199	3274	calcium channel,	ACTGGGTTAC[T/C]TTGACTATGC	M	T	C	F	L
				voltage-gated,
				alpha 1D subunit,
				DHP-sensitive
G956u8	WIAF-14194	HT2199	5127	calcium channel,	TGCCTCTCAA[C/T)AGTGACGGGA	S	C	T	N	N
				voltage-gated,
				alpha 1D subunit,
				DHP-sensitive
G956u9	WIAF-14195	HT2199	5173	calcium channel,	TGCTTTGGTT[C/T]GAACCGCTCT	N	C	T	R	*
				voltage-gated,
				alpha 1D subunit,
				DHP-sensitive
G956u10	WIAF-14200	HT2199	1437	calcium channel,	CAGATATCGT[A/G]GCTGAAGAGG	S	A	G	V	V
				voltage-gated,
				alpha 1D subunit,
				DHP-sensitive
G956u11	WIAF-14201	HT2199	2567	calcium channel,	ACCAAGCGCA[G/T]CACCTTTGAC	M	G	T	S	I
				voltage-gated,
				alpha 1D subunit,
				DHP-sensitive
G956u12	WIAF-14202	HT2199	4464	calcium channel,	TCACCTTTTT[C/T]CGTCTTTTCC	S	C	T	F	F
				voltage-gated,
				alpha 1D subunit,
				DHP-sensitive
G956u13	WIAF-14215	HT2199	6927	calcium channel,	GCTACAGCGA[C/T]GAAGAGCCAG	S	C	T	F	F
				voltage-gated,
				alpha 1D subunit,
				DHP-sensitive
G956u14	WIAF-14216	HT2199	6858	calcium channel,	CCCGAGCCAA[C/T]GCGGATGTGG	S	C	T	N	N
				voltage-gated,
				alpha 1D subunit,
				DHP-sensitive
G957u1	WIAF-12306	HT4229	915	calcium channel,	TACATCGAGC[G/A]TGCTTCATGA	M	G	A	?	R
				voltage-gated,
				alpha 1E subunit,
				alt. transcript 2
G957u2	WIAF-12309	HT4229	3555	calcium channel,	GCCACTACAT[C/T]GTGAACCTGC	S	C	T	I	I
				voltage-gated,
				alpha 1E subunit,
				alt. transcript 2
G957u3	WIAF-12310	HT4229	4116	calcium channel,	ATGTAGATCA[C/T]GAGAAAAACA	S	C	T	H	H
				voltage-gated,
				alpha 1E subunit,
				alt. transcript 2
G957u4	WIAF-12313	HT4229	5181	calcium channel,	AGAACGACAA[T/C]GAACGCTGCG	S	T	C	N	N
				voltage-gated,
				alpha 1E subunit,
				alt. transcript
G957u5	WIAF-12314	HT4229	5971	calcium channel,	TATGGACCCC[C/A]CCCATGACGG	S	G	A	T	T
				voltage-gated,
				alpha 1E subunit,
				alt. transcript 2
G957u6	WIAF-12315	HT4229	5985	calcium channel,	ATGACGGACA[G/T]TTCCAACAAC	M	G	T	Q	H
				voltage-gated,
				alpha 1E subunit,
				alt. transcript 2
G957u7	WIAF-12329	HT4229	3100	calcium channel,	GCTGGCAGCA[C/A]GCCTTGATGA	M	G	A	G	S
				voltage-gated,
				alpha 1E subunit,
				alt. transcript 2
G957u8	WIAF-12331	HT4229	6492	calcium channel,	CCCTCCTTTC[C/T]TACAGCTCCC	M	C	T	?	R
				voltage-gated,
				alpha 1E subunit,
				alt. transcript 2
G957u9	WIAF-12354	HT4229	3839	calcium channel,	AACGCTTTGC[G/C]AACCAACAAA	M	G	C	G	A
				voltage-gated,
				alpha 1E subunit,
				alt. transcript 2
G957u10	WIAF-12357	HT4229	4753	calcium channel,	TGACTTCATC[A/G]CCCTCATTCG	M	A	G	T	A
				voltage-gated,
				alpha 1E subunit,
				alt. transcript 2
G960u1	WIAF-12305	HT3336	1246	CACNB3, calcium	TTGATCCCCT[C/T]TCATGAGCCC	M	C	T	S	F
				channel, voltage
				dependent, beta
				3 subunit
G960u2	WIAF-12340	HT3336	1288	CACNB3, calcium	TGGACAGGAT[C/T]TTCACAGCGT	M	C	T	S	F
				channel, voltage
				dependent, beta
				3 subunit
G960u3	WIAF-12345	HT3336	641	CACNB3, calcium	AGGCTCTCTT[C/T]CACTTCCTCA	S	C	T	F	F
				channel, voltage
				dependent, beta
				3 subunit
G960u4	WIAF-12346	HT3336	576	CACNB3, calcium	CATCCCGCCT[G/A]TGGTCCTCCT	M	G	A	V	M
				channel, voltage
				dependent, beta
				3 subunit
C961u1	WIAF-12322	U95019	2037	CACNB2, calcium	ACTCTCCCTA[C/T]GTAGAGCCAA	S	C	T	Y	Y
				channel, voltage
				dependent, beta
				2 subunit
G961u2	WIAF-12347	U95019	2007	CACNB2, calcium	CATTTGACTC[G/A]GAAACCCAGG	S	G	A	S	S
				channel, voltage
				dependent, beta
				2 subunit
G962u1	WIAF-12324	U95020	1423	CACNB4, calcium	CCAATTGAAA[G/A]ACGAAGTCTA	M	G	A	R	K
				channel, voltage
				dependent, beta
				4 subunit
G962u2	WIAF-12342	U95020	167	CACNB4, calcium	GGACCAGGTT[G/T]AAAAGATCCG	M	G	T	L	F
				channel, voltage
				dependent, beta
				4 subunit
G962u3	WIAF-12350	U95020	1571	CACNB4, calcium	ACACTTACAA[A/C]CCCCATAGGA	S	A	G	K	K
				channel, voltage
				dependent, beta
				4 subunit
G965u1	WIAF-12312	U40583	1276	CHRNA7, cholinergic	TCCTGCACGC[T/C]GGCCAACCCC	S	T	C	G	G
				receptor,
				nicotinic, alpha
				polypeptide 7
G968a1	WIAF-12119	HT27592	1008	CHRNA1, cholinergic	ACACACACCA[C/T]CGCTCACCCA	S	C	T	H	H
				receptor,
				nicotinic, alpha
				polypeptide 1
				(muscle)
G968u2	WIAF-12368	HT27592	1136	CHRNA1, cholinergic	AAGATTTTTA[C/T]AGAACACATT	M	C	T	T	I
				receptor,
				nicotinic, alpha
				polypeptide 1
				(muscle)
G973a1	WIAF-13172	HT48774	800	CHRNA2, cholinergic	ACACTTCAGA[C/t]GTGGTGATTG	S	C	t	D	D
				receptor,
				nicotinic, alpha
				polypeptide 2
				(neuronal)
G973a2	WIAF-13173	HT48774	927	CHRNA2, cholinergic	CTGGAACCCC[G/a]CTCATTTTGC	M	G	a	A	T
				receptor,
				nicotinic, alpha
				polypeptide 2
				(neuronal)
G977u1	WIAF-13949	Y08419	366	CHRNA5, cholinergic	AACTTATACC[T/C]CTTCCTTCAC	S	T	C	R	R
				receptor,
				nicotinic, alpha
				polypeptide 5
G978a1	WIAF-13179	Y08417	1331	CHRNB3, cholinergic	CCATTAGATA[C/a]ATTTCCACAC	N	C	a	Y	*
				receptor,
				nicotinic, beta
				polypeptide 3
G983a1	WIAF-13214	HT0374	236	NPY, neuropeptide Y	CATACTACTC[C/A]CCCCTCCGAC	S	G	A	S	S
G983a2	WIAF-13215	HT0374	290	NPY, neuropeptide Y	CAAAACGATC[C/T]AGCCCAGAGA	S	C	T	S	S
G983a3	WIAF-13216	HT0374	111	NPY, neuropeptide Y	GCCACTCCCC[C/T]TCTCCGCACT	S	C	T	L	L
G987a1	WIAF-13174	HT27830	159	PPYR1, pancreatic	TGGTCTTCAT[C/T]GTCACTTCCT	S	C	T	I	I
				polypeptide
				receptor 1
G987a2	WIAF-13175	HT27830	222	PPYR1, pancreatic	TGATCTGTGT[G/A]ACTGTGAGGC	S	G	A	V	V
				polypeptide
				receptor 1
G987a3	WIAF-13176	HT27830	322	PPYR1, pancreatic	GCCGCTGACC[C/T]CCCTCTACAC	M	G	T	A	S
				polypeptide
				receptor 1
G987a4	WIAF-13177	HT27830	1074	PPYR1, pancreatic	TGGACGACTC[G/A]GACCATCTCC	S	G	A	S	S
				polypeptide,
				receptor 1
G987a5	WIAF-13178	HT27830	975	PPYR1, pancreatic	CCTCCACCTG[C/T]GTCAACCCAT	S	C	T	C	C
				polypeptide
				receptor 1
G987a6	WIAF-13180	HT27830	615	PPYR1, pancreatic	AGTTCCTCCC[A/g]GATAAGCTGC	S	A	g	A	A
				polypeptide
				receptor 1
G987a7	WIAF-13181	HT27830	718	PPYR1, pancreatic	GGGCTTCATC[C/T]TGGTCTGTTA	S	C	T	L	L
				polypeptide
				receptor 1
G987a8	WIAF-13182	HT27830	745	PPYR1, pancreatic	CATCTACCGG[C/t]GCCTGCAGAG	M	C	t	R	C
				polypeptide
				receptor 1
G987a9	WIAF-13183	HT27830	842	PPYR1, pancreatic	GTGATGCTCC[T/A]GGCCTTTGCC	M	T	A	V	E
				polypeptide
				receptor 1
G987a10	WIAF-13184	HT27830	852	PPYR1, pancreatic	TCGCCTTTGC[C/T]GTGCTCTGGC	S	C	T	A	A
				polypeptide
				receptor 1
G987a11	WIAF-13185	HT27830	889	PPYR1, pancreatic	CAACAGCCTG[G/a]AACACTCGCA	M	G	a	E	K
				polypeptide
				receptor 1
G987a12	WIAF-13186	HT27830	924	PPYR1, pancreatic	CCATCTGCCA[C/T]CCGAACCTCA	S	C	T	H	H
				polypeptide
				receptor 1
G989u1	WIAF-13573	D86519	891	NPY6R, neuro-	TGACTCATGC[C/T]TACTGGGCCA	S	C	T	A	A
				peptide Y receptor
				Y6
G989u2	WIAF-13588	D86519	465	NPY6R, neuro-	ACCACCCAGC[A/C]TCTAATACAA	S	A	G	A	A
				peptide Y receptor
				Y6
G989u3	WIAF-13591	D86519	980	NPY6R, neuro-	GAGCCCTTCC[G/A]CAACCTCTCT	M	G	A	R	H
				peptide Y receptor
				Y6
G991u1	WIAF-12390	HT97376	336	Notch2	AAGCTACTTG[C/T]GTTCAGAAAA	S	C	T	C	C
G993u1	WIAF-12359	U95299	1343	NOTCH4, Notch	TCCACACTCT[G/T]CCTGTGTCAG	H	G	T	C	F
				(Drosophila)
				homolog 4
G993u2	WIAF-12361	U95299	2020	NOTCH4, Notch	TAACCACCAC[A/C]AACACAACCC	H	A	G	K	E
				(Drosophila)
				homolog 4
G993u3	WIAF-12384	U95299	5775	NOTCH4, Notch	CCGCCTATTC[G/T]CATTGCCGGA	S	C	T	S	S
				(Drosophila)
				homolog 4
G996a1	WIAF-13213	HT3329	356	OPRM1, opioid	CTTAGATCCC[A/G]ACCTCTCCCA	M	A	G	N	D
				receptor, mu 1
LPLa4	WIAF-13314	HT1320	443	LPL, lipoprotein	ATGTATGACA[C/T]TTGCCTGCCA	M	C	T	S	I
				lipase
LPLa5	WIAF-13315	HT1320	579	LPL, lipoprotein	GACAGCATCT[G/A]GCCCGGTTTA	S	G	A	V	V
				lipase
LPLa6	WIAF-13316	HT1320	609	LPL, lipoprotein	TGGACGAGCA[C/A]TTTAACTACC	S	C	A	E	E
				lipase
LPLa7	WIAF-13317	HT1320	1338	LPL, lipoprotein	CAAATAAGAC[C/A]TACTCCTTCC	S	C	A	T	V
				lipase
LPLa8	WIAF-13318	HT1320	1117	LPL, lipoprotein	CAATCTGCCC[T/C]ATGAGATCAA	M	T	C	Y	D
				lipase
LPLa9	WIAF-13319	HT1320	715	LPL, lipoprotein	CAGAATTACT[G/A]GCCTCCATCC	M	C	A	C	S
				lipase
LPLa10	WIAF-13320	HT1320	834	LPL, lipoprotein	CTGGTCGAAC[C/A]ATTGGAATCC	M	C	A	S	R
				lipase
LPLa11	WIAF-13321	HT1320	951	LPL, lipoprotein	GACTTGCACA[T/A]CTCCACCAGC	M	T	A	D	E
				lipase
LPLa12	WIAF-13322	HT1320	1595	LPL, lipoprotein	AATAACAACT[C/C]AGCCTCAAAC	N	C	G	S	*
				lipase
LPLa13	WIAF-13323	HT1320	1597	LPL, lipoprotein	TAAGAAGTCA[G/A]GCTGAAACTG	M	G	A	G	S
				lipase
LPLa14	WIAF-13324	HT1320	1606	LPL, lipoprotein	AGGCTGAAAC[T/C]CGGCGAATCT	T	C	—	—
				lipase
LPLa15	WIAF-13325	HT1320	1611	LPL, lipoprotein	GAAACTGGGC[G/A]AATcTACAGA	—	G	A	—	—
				lipase

While this invention has been particularly shown and described with references to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention encompassed by the appended claims.