Genotyping the human phenol sulfotransferbase 2 gene STP2

Abstract

Genetic polymorphisms are identified in the human STP2 gene that alter STP2-dependent drug metabolism. Nucleic acids comprising the polymorphic sequences are used to screen patients for altered metabolism for STP2 substrates, potential drug-drug interactions, and adverse/side effects, as well as diseases that result from environmental or occupational exposure to toxins. The nucleic acids are used to establish animal, cell and in vitro models for drug metabolism.

Description

Sulfonation is an important pathway in the biotransformation of many drugs, xenobiotics, neurotransmitters, and steroid hormones. Many of the sulfonation reactions for pharmacologic agents are performed by a group of enzymes known as phenol transferases. The phenol sulfotransferase gene family consists to three members located on chromosome 16. A single gene (STM) encodes the thermolabile monoamine-metabolizing form. Two thermostable phenol-metabolizing enzymes are encoded by STP1 and STP2. Substrates for STP1 and STP2 include minoxidil, acetaminophen, and para-nitrophenol. Alterations in phenol sulfotransferase activity have been correlated with individual variation in sulfonation of acetaminophen (Reiter and Weinshilboum (1982) Clin. Pharm.) and predisposition to diet-induced migraine headaches.

The STP2 gene spans approximately 5.1 kb and contains nine exons that range in length from 74 to 347 bp. Exons IA and IB are noncoding and represent two different cDNA 5′-untranslated region sequences. The two apparent 5′-flanking regions of the STP2 gene contain no canonical TATA boxes, but do contain CCAAT elements. STP2 has been localized to human chromosome 16.

Since rates of metabolism of drugs, toxins, etc. can depend on the amounts and kinds of phenol sulfotransferase in tissues, variation in biological response may be determined by the profile of expression of phenol sulfotransferases in each person. Analysis of genetic polymorphisms that lead to altered expression and/or enzyme activity are therefore of interest.

SUMMARY OF THE INVENTION

Genetic sequence polymorphisms are identified in the STP2 gene. Nucleic acids comprising the polymorphic sequences are used in screening assays, and for genotyping individuals. The genotyping information is used to predict an individuals' rate of metabolism for STP2 substrates, potential drug-drug interactions, and adverse/side effects. Specific polynucleotides include the polymorphic STP2 sequences set forth in SEQ ID NOs:63-100.

The nucleic acid sequences of the invention may be provided as probes for detection of STP2 locus polymorphisms, where the probe comprises a polymorphic sequence of SEQ ID NOs:63-110. The sequences may further be utilized as an array of oligonucleotides comprising two or more probes for detection of STP2 locus polymorphisms.

Another aspect of the invention provides a method for detecting in an individual a polymorphism in STP2 metabolism of a substrate, where the method comprises analyzing the genome of the individual for the presence of at least one STP2 polymorphism; wherein the presence of the predisposing polymorphism is indicative of an alteration in STP2 expression or activity. The analyzing step of the method may be accomplished by detection of specific binding between the individual's genomic DNA with an array of oligonucleotides comprising STP2 locus polymorphic sequences. In other embodiments, the alteration in STP2 expression or activity is tissue specific, or is in response to a STP2 modifier that induces or inhibits STP2 expression.

Database References for Nucleotide Sequences

Genbank accession no. U34804 provides the sequence of the STP2 gene.

Brief Description of the Sequence Listing

STP2 Reference Sequences. SEQ ID NO:1 lists the sequence of the reference STP2 gene. The exons are as follows: exon 1A (nt 2591-2664); exon 1B (nt 3180-3526); exon 2 (nt 3726-3877); exon 3 (nt 3985-4110); exon 4 (nt 4196-4293); exon 5 (nt 6088-6214); exon 6 (6310-6404); exon 7 (nt 7214-7394); exon 8 (nt 7517-7712). The mRNA sequence is set forth in SEQ ID NO:2, and the encoded amino acid sequence in SEQ ID NO:3.

Primers. The PCR primers for amplification of polymorphic sequences are set forth as SEQ ID NOs:4-17. The primers used in sequencing isolated polymorphic sequences are presented as SEQ ID NOs:18-46. The primers used in Taqman assays are listed as SEQ ID NO:47-62.

Polymorphisms. Polymorphic sequences of STP2 are presented as SEQ ID NOs:63-110.

DESCRIPTION OF THE SPECIFIC EMBODIMENTS

Pharmacogenetics is the linkage between an individual's genotype and that individual's ability to metabolize or react to a therapeutic agent. Differences in metabolism or target sensitivity can lead to severe toxicity or therapeutic failure by altering the relation between bioactive dose and blood concentration of the drug. Relationships between polymorphisms in metabolic enzymes or drug targets-and both response and toxicity can be used to optimize therapeutic dose administration.

Genetic polymorphisms are identified in the STP2 gene. Nucleic acids comprising the polymorphic sequences are used to screen patients for altered metabolism for STP2 substrates, potential drug-drug interactions, and adverse/side effects, as well as diseases that result from environmental or occupational exposure to toxins. The nucleic acids are used to establish animal, cell culture and in vitro cell-free models for drug metabolism.

Definitions

It is to be understood that this invention is not limited to the particular methodology, protocols, cell lines, animal species or genera, constructs, and reagents described, as such may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention which will be limited only by the appended claims.

As used herein the singular forms “a”, “and”, and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “a construct” includes a plurality of such constructs and reference to “the STP2 nucleic acid” includes reference to one or more nucleic acids and equivalents thereof known to those skilled in the art, and so forth. All technical and scientific terms used herein have the same meaning as commonly understood to one of ordinary skill in the art to which this invention belongs unless clearly indicated otherwise.

STP2 reference sequence. The sequence of the STP2 gene may be accessed through Genbank as previously cited, and is provided in SEQ ID NO:1 and SEQ ID NO:2 (cDNA sequence). The amino acid sequence of STP2 is listed as SEQ ID NO:3. These sequences provide a reference for the polymorphisms of the invention. The nucleotide sequences provided herein differ from the published sequence at certain positions throughout the sequence. Where there is a discrepancy the provided sequence is used as a reference.

The term “wild-type” may be used to refer to the reference coding sequences of STP2, and the term “variant”, or “STP2 v ” to refer to the provided variations in the STP2 sequence. Where there is no published form, such as in the intron sequences, the term wild-type may be used to refer to the most commonly found allele. It will be understood by one of skill in the art that the designation as “wild-type” is merely a convenient label for a common allele, and should not be construed as conferring any particular property on that form of the sequence.

STP2 polymorphic sequences. It has been found that specific sites in the STP2 gene sequence are polymorphic, i.e. within a population, more than one nucleotide (G, A, T, C) is found at a specific position. Polymorphisms may provide functional differences in the genetic sequence, through changes in the encoded polypeptide, changes in mRNA stability, binding of transcriptional and translation factors to the DNA or RNA, and the like. The polymorphisms are also used as single nucleotide polymorphisms to detect association with, or genetic linkage to phenotypic variation in activity and expression of STP2.

SNPs are generally biallelic systems, that is, there are two alleles that an individual may have for any particular marker. SNPs, found approximately every kilobase, offer the potential for generating very high density genetic maps, which will be extremely useful for developing haplotyping systems for genes or regions of interest, and because of the nature of SNPS, they may in fact be the polymorphisms associated with the disease phenotypes under study. The low mutation rate of SNPs also makes them excellent markers for studying complex genetic traits.

Single nucleotide polymorphisms are provided in the STP2 promoter, intron and exon sequences. Table 4 and the corresponding sequence listing provide both forms of each polymorphic sequence. For example, SEQ ID NO:99 and 100 are the alternative forms of a single polymorphic site. The provided sequences also encompass the complementary sequence corresponding to any of the provided polymorphisms.

In order to provide an unambiguous identification of the specific site of a polymorphism, sequences flanking the polymorphic site are shown in Table 4, where the 5′ and 3′ flanking sequence is non-polymorphic, and the central position, shown in bold, is variable. It will be understood that there is no special significance to the length of non-polymorphic flanking sequence that is included, except to aid in positioning the polymorphism in the genomic sequence. The STP2 exon sequences have been published, and therefore one of each pair of sequences in Table 4 is a publically known sequence.

As used herein, the term “STP2 gene” is intended to generically refer to both the wild-type and variant forms of the sequence, unless specifically denoted otherwise. As it is commonly used in the art, the term “gene” is intended to refer to the genomic region encompassing 5′ UTR, exons, introns, and 3′ UTR. Individual segments may be specifically referred to, e.g. exon 2, intron 5, etc. Combinations of such segments that provide for a complete STP2 protein may be referred to generically as a protein coding sequence.

Nucleic acids of interest comprise the provided STP2 v nucleic acid sequence(s), as set forth in Table 4. Such nucleic acids include short hybridization probes, protein coding sequences, variant forms of STP2 cDNA, segments, e.g. exons, introns, etc., and the like. Methods of producing nucleic acids are well-known in the art, including chemical synthesis, cDNA or genomic cloning, PCR amplification, etc.

For the most part, DNA fragments will be of at least 15 nt, usually at least 20 nt, often at least 50 nt. Such small DNA fragments are useful as primers for PCR, hybridization screening, etc. Larger DNA fragments, i.e. greater than 100 nt are useful for production of the encoded polypeptide, promoter motifs, etc. For use in amplification reactions, such as PCR, a pair of primers will be used. The exact composition of primer sequences is not critical to the invention, but for most applications the primers will hybridize to the subject sequence under stringent conditions, as known in the art.

The STP2 nucleic acid sequences are isolated and obtained in substantial purity, generally as other than an intact or naturally occurring mammalian chromosome. Usually, the DNA will be obtained substantially free of other nucleic acid sequences that do not include a STP2 sequence or fragment thereof, generally being at least about 50%, usually at least about 90% pure and are typically “recombinant”, i.e. flanked by one or more nucleotides with which it is not normally associated on a naturally occurring chromosome.

For screening purposes, hybridization probes of the polymorphic sequences may be used where both forms are present, either in separate reactions, spatially separated on a solid phase matrix, or labeled such that they can be distinguished from each other. Assays may utilize nucleic acids that hybridize to one or more of the described polymorphisms.

An array may include all or a subset of the polymorphisms listed in Table 4. One or both polymorphic forms may be present in the array, for example the polymorphism of SEQ ID NO:37 and 38 may be represented by either, or both, of the listed sequences. Usually such an array will include at least 2 different polymorphic sequences, i.e. polymorphisms located at unique positions within the locus, and may include as many all of the provided polymorphisms. Arrays of interest may further comprise sequences, including polymorphisms, of other genetic sequences, particularly other sequences of interest for pharmacogenetic screening, e.g. STP1; UGT1, UGT2, cytochrome oxidases, etc. The oligonucleotide sequence on the array will usually be at least about 12 nt in length, may be the length of the provided polymorphic sequences, or may extend into the flanking regions to generate fragments of 100 to 200 nt in length. For examples of arrays, see Ramsay (1998) Nat. Biotech. 16:40-44; Hacia et al. (1996) Nature Genetics 14:441-447; Lockhart et al. (1996) Nature Biotechnol. 14:1675-1680; and De Risi et al. (1996) Nature Genetics 14:457-460.

Nucleic acids may be naturally occurring, e.g. DNA or RNA, or may be synthetic analogs, as known in the art. Such analogs may be preferred for use as probes because of superior stability under assay conditions. Modifications in the native structure, including alterations in the backbone, sugars or heterocyclic bases, have been shown to increase intracellular stability and binding affinity. Among useful changes in the backbone chemistry are phosphorothioates; phosphorodithioates, where both of the non-bridging oxygens are substituted with sulfur; phosphoroamidites; alkyl phosphotriesters and boranophosphates. Achiral phosphate derivatives include 3′-O′-5′-S-phosphorothioate, 3′-S-5′-O-phosphorothioate, 3′-CH2-5′-O-phosphonate and 3′-NH-5′-O-phosphoroamidate. Peptide nucleic acids replace the entire ribose phosphodiester backbone with a peptide linkage.

Sugar modifications are also used to enhance stability and affinity. The a-anomer of deoxyribose may be used, where the base is inverted with respect to the natural b-anomer. The 2′-OH of the ribose sugar may be altered to form 2′-O-methyl or 2′-O-allyl sugars, which provides resistance to degradation without comprising affinity.

Modification of the heterocyclic bases must maintain proper base pairing. Some useful substitutions include deoxyuridine for deoxythymidine; 5-methyl-2′-deoxycytidine and 5-bromo-2′-deoxycytidine for deoxycytidine. 5-propynyl-2′-deoxyuridine and 5-propynyl-2′-deoxycytidine have been shown to increase affinity and biological activity when substituted for deoxythymidine and deoxycytidine, respectively.

STP2 polypeptides. A subset of the provided nucleic acid polymorphisms in STP2 exons confer a change in the corresponding amino acid sequence. Using the amino acid sequence provided in SEQ ID NO:3 as a reference, the amino acid polymorphisms of the invention include pro→leu, pos. 19; ala→val, pos.136; asn→thr, pos. 235; glu→lys, pos 282; and a truncated form resulting from a stop codon at exon 5, position 447. Polypeptides comprising at least one of the provided polymorphisms (STP2 v polypeptides) are of interest. The term “STP2 v polypeptides” as used herein includes complete STP2 protein forms, e.g. such splicing variants as known in the art, and fragments thereof, which fragments may comprise short polypeptides, epitopes, functional domains; binding sites; etc.; and including fusions of the subject polypeptides to other proteins or parts thereof. Polypeptides will usually be at least about 8 amino acids in length, more usually at least about 12 amino acids in length, and may be 20 amino acids or longer, up to substantially the complete protein.

The STP2 genetic sequence, including polymorphisms, may be employed for polypeptide synthesis. For expression, an expression cassette may be employed, providing for a transcriptional and translational initiation region, which may be inducible or constitutive, where the coding region is operably linked under the transcriptional control of the transcriptional initiation region, and a transcriptional and translational termination region. Various transcriptional initiation regions may be employed that are functional in the expression host. The polypeptides may be expressed in prokaryotes or eukaryotes in accordance with conventional ways, depending upon the purpose for expression. Small peptides can also be synthesized in the laboratory.

Substrate. A substrate is a chemical entity that is modified by STP2, usually under normal physiological conditions. Although the duration of drug action tends to be shortened by metabolic transformation, drug metabolism is not “detoxification”. Frequently the metabolic product has greater biologic activity than the drug itself. In some cases the desirable pharmacologic actions are entirely attributable to metabolites, the administered drugs themselves being inert. Likewise, the toxic side effects of some drugs may be due in whole or in part to metabolic products.

Substrates of interest may be drugs, xenobiotics, neurotransmitters, steroid hormones, etc. STP2 preferentially catalyzes the sulfonation of ‘simple’ planar phenols. Substrates include minoxidil, acetaminophen, para-nitrophenol, N-hydroxy 4-aminobiphenyl, etc.

Modifier. A modifier is a chemical agent that modulates the action of STP2, either through altering its enzymatic activity (enzymatic modifier) or through modulation of expression (expression modifier, e.g., by affecting transcription or translation). In some cases the modifier may also be a substrate. Inhibitors include N-ethylmaleimide; phenylglyoxal; 2,6-dichloro-4-nitrophenol; p-nitrophenol; quercetin and other flavonoids, e.g. fisetin, galangin, myricetin, kaempferol, chrysin, apigenin; and phenols such as curcumin, genistein, ellagic acid. Steroids, e.g. estradiol benzoate, testosterone proprionate may affect activity and/or expression.

Pharmacokinetic parameters. Pharmacokinetic parameters provide fundamental data for designing safe and effective dosage regimens. A drug's volume of distribution, clearance, and the derived parameter, half-life, are particularly important, as they determine the degree of fluctuation between a maximum and minimum plasma concentration during a dosage interval, the magnitude of steady state concentration and the time to reach steady state plasma concentration upon chronic dosing. Parameters derived from in vivo drug administration are useful in determining the clinical effect of a particular STP2 genotype.

Expression assay. An assay to determine the effect of a sequence polymorphism on STP2 expression. Expression assays may be performed in cell4ree extracts, or by transforming cells with a suitable vector. Alterations in expression may occur in the basal level that is expressed in one or more cell types, or in the effect that an expression modifier has on the ability of the gene to be inhibited or induced. Expression levels of a variant alleles are compared by various methods known in the art. Methods for determining promoter or enhancer strength include quantitation of the expressed natural protein; insertion of the variant control element into a vector with a reporter gene such as β-galactosidase, luciferase, chloramphenicol acetyltransferase, etc. that provides for convenient quantitation; and the like.

Gel shift or electrophoretic mobility shift assay provides a simple and rapid method for detecting DNA-binding proteins (Ausubel, F. M. et al. (1989) In: Current Protocols in Molecular Biology, Vol. 2, John Wiley and Sons, New York). This method has been used widely in the study of sequence-specific DNA-binding proteins, such as transcription factors. The assay is based on the observation that complexes of protein and DNA migrate through a nondenaturing polyacrylamide gel more slowly than free DNA fragments or double-stranded oligonucleotides. The gel shift assay is performed by incubating a purified protein, or a complex mixture of proteins (such as nuclear or cell extract preparations), with an end-labeled DNA fragment containing the putative protein binding site. The reaction products are then analyzed on a nondenaturing polyacrylamide gel. The specificity of the DNA-binding protein for the putative binding site is established by competition experiments using DNA fragments or oligonucleotides containing a binding site for the protein of interest, or other unrelated DNA sequences.

Expression assays can be used to detect differences in expression of polymorphisms with respect to tissue specificity, expression level, or expression in response to exposure to various substrates, and/or timing of expression during development. For example, since STP2 is expressed in liver, polymorphisms could be evaluated for expression in tissues other than liver, or expression in liver tissue relative to a reference STP2 polypeptide.

Substrate screening assay. Substrate screening assays are used to determine the metabolic activity of a STP2 protein or peptide fragment on a substrate. Many suitable assays are known in the art, including the use of primary or cultured cells, genetically modified cells (e.g., where DNA encoding the STP2 polymorphism to be studied is introduced into the cell within an artificial construct), cell-free systems, e.g. microsomal preparations or recombinantly produced enzymes in a suitable buffer, or in animals, including human clinical trials. Where genetically modified cells are used, since most cell lines do not express STP2 activity (liver cells lines being the exception), introduction of artificial construct for expression of the STP2 polymorphism into many human and non-human cell lines does not require additional modification of the host to inactivate endogenous STP2 expression/activity. Clinical trials may monitor serum, urine, etc. levels of the substrate or its metabolite(s).

Typically a candidate substrate is input into the assay system, and the oxidation to a metabolite is measured over time. The choice of detection system is determined by the substrate and the specific assay parameters. Assays are conventionally run, and will include negative and positive controls, varying concentrations of substrate and enzyme, etc. Exemplary assays may be found in the literature, for examples see Chou et al. (1995) Carcinogenesis 16:413-417; Walle and Walle (1991) Drug Metab. Dispos. 19:448-453; and Falany et al.. (1990) Arch. Biochem. Biophys. 278:312-318.

Genotyping: STP2 genotyping is performed by DNA or RNA sequence and/or hybridization analysis of any convenient sample from a patient, e.g. biopsy material, blood sample (serum, plasma, etc.), buccal cell sample, etc. A nucleic acid sample from an individual is analyzed for the presence of polymorphisms in STP2, particularly those that affect the activity or expression of STP2. Specific sequences of interest include any polymorphism that leads to changes in basal expression in one or more tissues, to changes in the modulation of STP2 expression by modifiers, or alterations in STP2 substrate specificity and/or activity.

Linkage Analysis: Diagnostic screening may be performed for polymorphisms that are genetically linked to a phenotypic variant in STP2 activity or expression, particularly through the use of microsatellite markers or single nucleotide polymorphisms (SNP). The microsatellite or SNP polymorphism itself may not phenotypically expressed, but is linked to sequences that result in altered activity or expression. Two polymorphic variants may be in linkage disequilibrium, i.e. where alleles show non-random associations between genes even though individual loci are in Hardy-Weinberg equilibrium.

Linkage analysis may be performed alone, or in combination with direct detection of phenotypically evident polymorphisms. The use of microsatellite markers for genotyping is well documented. For examples, see Mansfield et al. (1994) Genomics 24:225-233; and Ziegle et al. (1992) Genomics 14:1026-1031. The use of SNPs for genotyping is illustrated in Underhill et al. (1996) Proc Natl Acad Sci U S A 93:196-200.

Transgenic animals. The subject nucleic acids can be used to generate genetically modified non-human animals or site specific gene modifications in cell lines. The term “transgenic” is intended to encompass genetically modified animals having a deletion or other knock-out of STP2 gene activity, having an exogenous STP2 gene that is stably transmitted in the host cells, or having an exogenous STP2 promoter operably linked to a reporter gene. Transgenic animals may be made through homologous recombination, where the STP2 locus is altered. Alternatively, a nucleic acid construct is randomly integrated into the genome. Vectors for stable integration include plasmids, retroviruses and other animal viruses, YACs, and the like. Of interest are transgenic mammals, e.g. cows, pigs, goats, horses, etc., and particularly rodents, e.g. rats, mice, etc.

Genetically Modified Cells. Primary or cloned cells and cell lines are modified by the introduction of vectors comprising STP2 gene polymorphisms. The gene may comprise one or more variant sequences, preferably a haplotype of commonly occurring combinations. In one embodiment of the invention, a panel of two or more genetically modified cell lines, each cell line comprising a STP2 polymorphism, are provided for substrate and/or expression assays. The panel may further comprise cells genetically modified with other genetic sequences, including polymorphisms, particularly other sequences of interest for pharmacogenetic screening, e.g. STP1; UGT1, UGT2, cytochrome oxidases, etc.

Vectors useful for introduction of the gene include plasmids and viral vectors, e.g. retroviral-based vectors, adenovirus vectors, etc. that are maintained transiently or stably in mammalian cells. A wide variety of vectors can be employed for transfection and/or integration of the gene into the genome of the cells. Alternatively, micro-injection may be employed, fusion, or the like for introduction of genes into a suitable host cell.

Genotyping Methods

The effect of a polymorphism in the STP2 gene sequence on the response to a particular substrate or modifier of STP2 is determined by in vitro or in vivo assays. Such assays may include monitoring the metabolism of a substrate during clinical trials to determine the STP2 enzymatic activity, specificity or expression level. Generally, in vitro assays are useful in determining the direct effect of a particular polymorphism, while clinical studies will also detect an enzyme phenotype that is genetically linked to a polymorphism.

The response of an individual to the substrate or modifier can then be predicted by determining the STP2 genotype, with respect to the polymorphism. Where there is a differential distribution of a polymorphism by racial background, guidelines for drug administration can be generally tailored to a particular ethnic group.

The basal expression level in different tissue may be determined by analysis of tissue samples from individuals typed for the presence or absence of a specific polymorphism. Any convenient method may be use, e.g. ELISA, RIA, etc. for protein quantitation, northern blot or other hybridization analysis, quantitative RT-PCR, etc. for mRNA quantitation. The tissue specific expression is correlated with the genotype.

The alteration of STP2 expression in response to a modifier is determined by administering or combining the candidate modifier with an expression system, e.g. animal, cell, in vitro transcription assay, etc. The effect of the modifier on STP2 transcription and/or steady state mRNA levels is determined. As with the basal expression levels, tissue specific interactions are of interest. Correlations are made between the ability of an expression modifier to affect STP2 activity, and the presence of the provided polymorphisms. A panel of different modifiers, cell types, etc. may be screened in order to determine the effect under a number of different conditions.

A STP2 polymorphism that results in altered enzyme activity or specificity is determined by a variety of assays known in the art. The enzyme may be tested for metabolism of a substrate in vitro, for example in defined buffer, or in cell or subcellular lysates, where the ability of a substrate to be metabolized by STP2 under physiologic conditions is determined. Where there are not significant issues of toxicity from the substrate or metabolite(s), in vivo human trials may be utilized, as previously described.

The genotype of an individual is determined with respect to the provided STP2 gene polymorphisms. The genotype is useful for determining the presence of a phenotypically evident polymorphism, and for determining the linkage of a polymorphism to phenotypic change.

A number of methods are available for analyzing nucleic acids for the presence of a specific sequence. Where large amounts of DNA are available, genomic DNA is used directly. Alternatively, the region of interest is cloned into a suitable vector and grown in sufficient quantity for analysis. The nucleic acid may be amplified by conventional techniques, such as the polymerase chain reaction (PCR), to provide sufficient amounts for analysis. The use of the polymerase chain reaction is described in Saiki et al. (1985) Science 230:1350-1354, and a review of current techniques may be found in Sambrook et al. Molecular Cloning:. A Laboratory Manual, CSH Press 1989, pp.14.2-14.33. Amplification may be used to determine whether a polymorphism is present, by using a primer that is specific for the polymorphism. Alternatively, various methods are known in the art that utilize oligonucleotide ligation as a means of detecting polymorphisms, for examples see Riley et al. (1990) Nucleic Acids Res 18:2887-2890; and Delahunty et al. (1996) Am J Hum Genet 58:1239-1246.

A detectable label may be included in an amplification reaction. Suitable labels include fluorochromes, e.g. fluorescein isothiocyanate (FITC), rhodamine, Texas Red, phycoerythrin, allophycocyanin, 6-carboxyfluorescein (6-FAM), 2′,7′-dimethoxy-4′,5′-dichloro-6-carboxyfluorescein (JOE), 6-carboxy-X-rhodamine (ROX), 6-carboxy-2′,4′,7′,4,7-hexachlorofluorescein (HEX), 5-carboxyfluorescein (5-FAM) or N,N,N′,N′-tetramethyl-6-carboxyrhodamine (TAMRA), radioactive labels, e.g. 32P, 35S, 3H; etc. The label may be a two stage system, where the amplified DNA is conjugated to biotin, haptens, etc. having a high affinity binding partner, e.g. avidin, specific antibodies, etc., where the binding partner is conjugated to a detectable label. The label may be conjugated to one or both of the primers. Alternatively, the pool of nucleotides used in the amplification is labeled, so as to incorporate the label into the amplification product.

The sample nucleic acid, e.g. amplified or cloned fragment, is analyzed by one of a number of methods known in the art. The nucleic acid may be sequenced by dideoxy or other methods. Hybridization with the variant sequence may also be used to determine its presence, by Southern blots, dot blots,,etc. The hybridization pattern of a control and variant sequence to an array of oligonucleotide probes immobilized on a solid support, as described in U.S. Pat. No. 5,445,934, or in WO95/35505, may also be used as a means of detecting the presence of variant sequences. Single strand conformational polymorphism (SSCP) analysis, denaturing gradient gel electrophoresis (DGGE), mismatch cleavage detection, and heteroduplex analysis in gel matrices are used to detect conformational changes created by DNA sequence variation as alterations in electrophoretic mobility. Alternatively, where a polymorphism creates or destroys a recognition site for a restriction endonuclease (restriction fragment length polymorphism, RFLP), the sample is digested with that endonuclease, and the products size fractionated to determine whether the fragment was digested. Fractionation is performed by gel or capillary electrophoresis, particularly acrylamide or agarose gels.

In one embodiment of the invention, an array of oligonucleotides are provided, where discrete positions on the array are complementary to one or more of the provided polymorphic sequences, e.g. oligonucleotides of at least 12 nt, frequently 20 nt, or larger, and including the sequence flanking the polymorphic position. Such an array may comprise a series of oligonucleotides, each of which can specifically hybridize to a different polymorphism. For examples of arrays, see Hacia et al. (1996) Nat Genet 14:441-447 and DeRisi et al. (1996) Nat Genet 14:457-460.

The genotype information is used to predict the response of the individual to a particular STP2 substrate or modifier. Where an expression modifier inhibits STP2 expression, then drugs that are a STP2 substrate will be metabolized more slowly if the modifier is co-administered. Where an expression modifier induces STP2 expression, a co-administered substrate will typically be metabolized more rapidly. Similarly, changes in STP2 activity will affect the metabolism of an administered drug. The pharmacokinetic effect of the interaction will depend on the metabolite that is produced, e.g. a prodrug is metabolized to an active form, a drug is metabolized to an inactive form, an environmental compound is metabolized to a toxin, etc. Consideration is given to the route of administration, drug-drug interactions, drug dosage, etc.

Experimental

The following examples are put forth so as to provide those of ordinary skill in the art with a complete disclosure and description of how to make and use the subject invention, and are not intended to limit the scope of what is regarded as the invention.

Efforts have been made to ensure accuracy with respect to the numbers used (e.g. amounts, temperature, concentrations, etc.) but some experimental errors and deviations should be allowed for. Unless otherwise indicated, parts are parts by weight, molecular weight is average molecular weight, temperature is in degrees centigrade; and pressure is at or near atmospheric.

Materials and Methods

DNA samples. Blood specimens from approximately 300 individuals were collected after obtaining informed consent. All samples were stripped of personal identifiers to maintain confidentiality. The only data associated with a given blood sample was gender and self-reported major racial group designations in the United States (Caucasian, Hispanic, African American). Genomic DNA was isolated from these samples using standard techniques. gDNA was either stored as concentrated solutions or stored dried in microtiter plates for future use.

PCR amplifications. The primers used to amplify the coding regions and the promoter region of the STP2 gene from 200 ng of human gDNA are shown in Table 1. Primers were designed based upon publicly available genomic sequence provided by Her et al. (1996) Genomics 33:409-420. 100 ng of gDNA from 2 individuals was amplified with the Perkin Elmer GeneAmp PCR kit according to manufacturer's instructions in 100 μl reactions with Taq Gold DNA polymerase, with two exceptions.

Boehringer-Mannheim Expand High Fidelity PCR System kit was used to amplify the promoter region and exon 1A. Magnesium concentrations for each PCR reaction was optimized empirically, and are shown in Table 1.

TABLE 1
PCR primers and AAg++ concentrations.
	For-
	ward/
	Re-	SEQ
Region	verse	ID	Forward Primer (5′ 3′)	[AAg ++ ]
Promoter	F	4.	CCCAAATACAGGTGTTCC	2 mAA
	R	5.	GGAGCAGAGCAAGGATC
Exon IA	F	6.	TTCTTCTAGGATCTTCTATCG	2 mAA
	R	7.	ACTCAGCAAAAGGAGGAT
Exon 1B	F	8.	TTAGAGATGGGGTCTTCC	2 mAA
	R	9.	GGGCGAGAGATGTCC
Exon 2	F	10.	GGAGAGGAGCCTACTGG	2 mAA
	R	11.	AGTCTGAGGTGAGCAT
Exons 3 & 4	F	12.	GCCTCAGTGACTTCCCT	3 mAA
	R	13.	TTTGGAAGAGACTTATCTGG
Exons 5 & 6	F	14.	GCAGGACTTTGGCTTT	2 mAA
	R	15.	GACTCAGGCACAGGAG
Exons 7 & 8	F	16.	GACCATCCCAGTCCTT	2 mAA
	R	17.	CCCCAACGACACAGG

Thermal cycling was performed in a GeneAmp PCR System 9600 PCR machine (Perkin Elmer) with an initial denaturation step at 95° C. for 10 min, followed by 35 cycles of denaturation at 95° C. for 30 sec, primer annealing at 60° C. for 45 sec, and primer extension at 72° C. for 2 min, followed by final extension at 72° C. for 5 min, with the following exceptions. 40 cycles were used to amplify exon 1 B and to co-amplify exons 7 and 8. Cycling conditions for the promoter region and exon 1A were an initial denaturation at 95° C. for 2 min, followed by 40 cycles of denaturation at 94° C. for 30 sec, primer annealing at 60° C. for 45 sec, and primer extension at 68° C. for 4 min, followed by a final extension at 68° C. for 7 min.

DNA sequencing. PCR products from 32 individuals, approximately ⅓ from each of the 3 major racial groups (see above), were spin column purified using Microcon-100 columns. Cycle sequencing was performed on the GeneAmp PCR System 9600 PCR machine (Perkin Elmer) using the ABI Prism dRhodamine Terminator Cycle Sequencing Ready Reaction Kit according to the manufacturer's directions. Oligonucleotide primers used for the sequencing reactions are listed in Table 2.

TABLE 2
Sequencing primers.
	For-
	ward/	SEQ
Region	Reverse	ID	Forward Primer (5′ 3′)
Promoter (1)	F	18.	TGGAGCCCGTCTTGG
	R	19.	CAGCAGTTTCACTTGACC
Promoter (2)	F	20.	TGCCACCCCCTGCT
	R	21.	AGGCTGCTCCCCTG
Promoter (3)	F	22.	GGGCTCACGCAACC
	R	23.	GCAGGTACTTTTCTTTCCA
Exon 1A (1)	F	24.	TTCTTCTAGGATCTTCTATCG
	R	25.	TTTTTGAGGTGTCACTGG
Exon IA (2)	F	26.	CCCACACAACACCCAC
	R	27.	GCTTCTGGAATGTTGG
Exon 1A (3)	R	28.	CGGAAAAAAAAAAAGGAAG
Exon 1B (1)	F	29.	CAATGCTGCCCAGA
	R	30.	GCTCCACTGAGGAACCT
Exon 1B (2)	F	31.	GGAGAGGAGCCTACTGG
	R	32.	TACCACCATCACAACAGC
Exon 2	F	33.	CTGAAAGCAAGAAATCCAC
	R	34.	AGGCTGAGGTGAGCAT
Exons 3 & 4	F	35.	GCGGTGACCTGGAA
	R	36.	TTTGGAAGAGACTTATCTGG
Exons 5 & 6 (1)	F	37.	CTGACTTGCCCCTACCT
	R	38.	TAGCCACCACCCCTTA
Exons 5 & 6 (2)	F	39.	CCAAAGTGTACCCTCACC
	R	40.	AGCCTGCTGCCACA
Exons 7 & 8 (1)	F	41.	GACCATCCCAGTCCTT
	R	42.	CAAACCCCCGTGCT
Exons 7 & 8 (2)	F	43.	CTGTGGACCTCTTGGTTG
	R	44.	CACAAATCATACTTTATTCTGG
Exons 7 & 8 (3)	F	45.	CGATGCGGACTATGC
	R	46.	CCCCAACGACACAGG

Eight μl sequencing reactions were subjected to 30 cycles at 96° C. for 20 sec, 50° C. for 20 sec, and 60° C. for 4 min, followed by ethanol precipitation. Samples were evaporated to dryness at 50° C. for ˜15 min and resuspended in 2 μl of loading buffer (5:1 deionized formamide:50 mM EDTA pH 8.0), heated to 65° C. for 5 min, and electrophoresed through 4% polyacrylamide/6M urea gels in an ABI 377 Nucleic Acid Analyzer according to the manufacturer's instructions for sequence determination. All sequences were determined from both the 5′ and 3′ (sense and antisense) direction. Each sequencing reaction was performed with 2 individuals' DNA pooled together. The 16 electropherograms were analyzed by comparing peak heights, looking for ˜25% reduction in peak size and/or presence of extra peaks as an indication of heterozygosity. If polymorphisms were identified, pools were subsequently split and resequenced for confirmation.

Population genotyping. High-throughput genotyping using TaqMan technology (ABI) was performed using standard techniques (Livak et al. (1995) PCR Methods and Applications 4:357-362) on the samples described above for 3 STP2 polymorphisms. Oligonucleotide PCR primers and probes used for genotyping are shown in Table 3. Polymorphisms for which allele frequencies were determined are marked with an asterisk (*) in Table 4.

TABLE 3
TaqAAan primers and probes.
SEQ
ID	Description	Primers
47.	STP2-136A	GGTGCTGGGGTTGAGTCTTCTG
	primer
48.	STP2-	CAAAGGATGTGGCGGTTTCCTACTACC
	136Ala
	probe
49.	STP2-136B	ACACCTTCCTTCCTCCCATCAAG
	primer
50.	STP2-	CGCAAAGGATGTGGTGGTTTCCTACTAC
	136Val
	probe
51.	STP2-235A	GGAGACTGTGGACCTCATGGTTGA
	primer
52.	STP2-	TAGTTGGTCATAGGGTTCTTCTTCATCTCCTT
	235Asn
	probe
53.	STP2-235B	CCGGCACCTACCTTTCCTCAT
	primer
54.	STP2-	TAGTTGGTCATAGGGGTCTTCTTCATCTCC
	235Thr
	probe
55.	STP2-282A	AGCTTTGCTCCCTGCCTTCCT
	primer
56.	STP2-	CTGCCATCTTCTCCGCATAGTCCG
	282Glu
	probe
57.	STP2-282B	GGAACCCCTCTCACAGCTCAGA
	primer
58.	STP2-	TGCCATCTTCTTCGCATAGTCCGC
	282Lys
	probe
59.	STP2-447A	GGTGCTGGGGTTGAGTCTTCTG
	primer
60.	STP2-	ATGGCCAAAGTGTACCCTCACCCTG
	DelA447
	probe
61.	STP2-447B	ACACCTTCCTTCCTCCCATCAAG
	primer
62.	STP2-	CATGGCCAAAGTGTAACCCTCACCC
	InsA447
	probe

Assay name is given by locus and position. Primer names are abbreviated locus-position and letter designations representing forward (A) and reverse (B) primers. Probes are abbreviated locus-position and 3 letter nucleic acid designations representing the nucleic acid alteration in the coding strand of the genomic DNA. Positions at which probes detect nucleic acid variations are shown in bold.

RESULTS

Eight exons, the promoter region, 3′ and 5′ untranslated regions from the human STP2 gene were resequenced in 32 individuals representing three major ethnic groups (Caucasian, Hispanic, and African American). The polymorphisms are listed in Table 4.

TABLE 4
Newly identified STP2 gene polymorphisms.
	SEQ		AA
Location;	ID	Polymorphism Sequence	change
3′ end; 99	63.	CCAGCTCCTCAACTTGCCCTG
	64.	CCAGCTCCTCTACTTGCCCTG
3′ TTTR; 7	65.	GTGAGAGGGGTTCCTGGAGTC
	66.	GTGAGAGGGGCTCCTGGAGTC
Promoter; -603	67.	CATGAAGCTGGGGCTGGCTCC
	68.	CATGAAGCTGAGGCTGGCTCC
Promoter; -833	69.	CTCGTGCCCAGGTTGACCCTG
	70.	CTCGTGCCCAAGTTGACCCTG
Promoter; -1005	71.	GGGATTCCTCAGGGGCACAGA
	72.	GGGATTCCTCCGGGGCACAGA
Promoter; -1306	73.	ACAGCGCCATGTTGCTTCTGG
	74.	ACAGCGCCATATTGCTTCTGG
5′ TTTR - A; 36	75.	CAGCCACTGCGGGCGAGGAGG
	76.	CAGCCACTGCAGGCGAGGAGG
5′ TTTR - A; 51	77.	AGGAGGGCACAAGGCCAGGTT
	78.	AGGAGGGCACGAGGCCAGGTT
5′ TTTR - B; 183	79.	GGGGAACATCGGGGAGAGGAG
	80.	GGGGAACATCAGGGAGAGGAG
Exon 5*; 447	81.	CCAAAGTGTACCCTCACCCT	INS
			STOP
	82.	CCAAAGTGTAACCCTCACCCT	INS
			STOP
Exon 5*; 136 (nt	83.	AAGGATGTGGCGGTTTCCTAC	ALA-
307)			VAL
	84.	AAGGATGTGGTGGTTTCCTAC	ALA-
			VAL
Exon 7*; 235 (nt	85.	ATGAAGAAGAACCCTATGACC	ASN-
705)			THR
	86.	ATGAAGAAGACCCCTATGACC	ASN-
			THR
Exon 8*; 282 (nt	87.	GGACTATGCGGAGAAGATGGC	GLTT-
845)			LYS
	88.	GGACTATGCGAAGAAGATGGC	GLTT-
			LYS
Exon 2; 19 (nt	89.	AAGGGGGTCCCGCTCATCAAG	PRO-
56)			LETT
	90.	AAGGGGGTCCTGCTCATCAAG	PRO-
			LETT
Intron 1A; 88	91.	CTCTGTTATCTCTGCCCTCTC
	92.	CTCTGTTATCCCTGCCCTCTC
Intron 2; 34	93.	CTCTCCCAGGTGGCAGTCCCC
	94.	CTCTCCCAGGCGGCAGTCCCC
Intron 4; -71	95.	CCTTTGCCAACAAGAGATG	DEL A
	96.	CCTTTGCCAACAAGAGATG	DEL A
Intron 5; -19	97.	GTGTCGGCACTCCCTGCCCGC
	98.	GTGTCGGCACCCCCTGCCCGC
Intron 6; 93	99.	CCTCCCTGGGCGGCCCCTCCA
	100.	CCTCCCTGGGTGGCCCCTCCA
Promoter; -547	101.	TTGGTCTATGGATCCATGCTC
	102.	TTGGTCTATGCATCCATGCTC
Promoter; -453	103.	CATGGGCTGCTGGAGGCCTGT
	104.	CATGGGCTGCCGGAGGCCTGT
Promoter; -425	105.	ACTGGGCCAGGACCCCTGGCA
	106.	ACTGGGCCAGAACCCCTGGCA
Promoter; -358	107.	CCTGCCTATCCCAGCTTTCTC
	108.	CCTGCCTATCTCAGCTTTCTC
Promoter; -355	109.	GCCTATCCCATCTTTCTCCTC
	110.	GCCTATCCCAGCTTTCTCCTC

Genotyping of 95 individuals from each of 3 broadly defined racial groups (African Americans, Hispanic Americans, and Caucasian Americans) for three polymorphisms produced the allele and genotype frequencies shown in Table 5.

TABLE 5
Allele and Genotype Population Frequencies. Polymorphism name includes gene abbreviation followed by nucleotide designation
for allele 1, then nucleotide number, then nucleotide designation for allele 2. Population abbreviations are as follows:
AfAm = African Americans; BAH = Caucasians from the United States; Cauc = Caucasians from California;
Hisp = Hispanics from California. Allele names are designated by nucleotide and position. Genotypes are designated by position
and 2 nucleotides representing each of the chromosomes in a given individual.
	Start
Locus Calc Name	Position	Population	Allele Freq	Genotype Freq
STP2 STP2_Ala136Val_AfAm	0	African Americans, California	STP2_Ala136 = 0.997	STP2_136Ala/Ala = 0.995
			STP2_Val136 = 0.003	STP2_136Ala/Val = 0.005
				STP2_136Val/Val = 0
STP2 STP2_Ala136Val_Cauc2	0	Caucasion, USA	STP2_Ala136 = 1	STP2_136Ala/Ala = 1
			STP2_Val136 = 0	STP2_136Ala/Val = 0
				STP2_136Val/Val = 0
STP2 STP2_Ala136Val_Cauc	0	Caucasion, California	STP2_Ala136 = 1	STP2_136Ala/Ala = 1
			STP2_Val136 = 0	STP2_136Ala/Val = 0
				STP2_136Val/Val = 0
STP2 STP2_Ala136Val_Chin	0	Chinese, California	STP2_Ala136 = 1	STP2_136Ala/Ala = 1
			STP2_Val136 = 0	STP2_136Ala/Val = 0
				STP2_136Val/Val = 0
STP2 STP2_Ala136Val_Hisp	0	Hispanics, California	STP2_Ala136 = 1	STP2_136Ala/Ala = 1
			STP2_Val136 = 0	STP2_136Ala/Val = 0
				STP2_136Val/Val = 0
STP2 STP2_Ala136Val_Japn	0	Japanese, California	STP2_Ala136 = 1	STP2_136Ala/Ala = 1
			STP2_Val136 = 0	STP2_136Ala/Val = 0
				STP2_136Val/Val = 0
STP2 STP2_insA447_AfAm	0	African Americans, California	STP2_delA447 = 0.981	STP2_447delA/delA = 0.963
			STP2_insA447 = 0.019	STP2_447delA/insA = 0.007
				STP2_447insA/insA = 0
STP2 STP2_insA447_Cauc2	0	Caucasion, USA	STP2_delA447 = 1	STP2_447delA/delA = 1
			STP2_insA447 = 0	STP2_447delA/insA = 0
				STP2_447insA/insA = 0
STP2 STP2_insA447_Cauc	0	Caucasion, California	STP2_delA447 = 1	STP2_447delA/delA = 1
			STP2_insA447 = 0	STP2_447delA/insA = 0
				STP2_447insA/insA = 0
STP2 STP2_insA447_Chin	0	Chinese, California	STP2_delA447 = 1	STP2_447delA/delA = 1
			STP2_insA447 = 0	STP2_447delA/insA = 0
				STP2_447insA/insA = 0
STP2 STP2_insA447_Hisp	0	Hispanics, California	STP2_delA447 = 0.995	STP2_447delA/delA = 0.989
			STP2_insA447 = 0.005	STP2_447delA/insA = 0.011
				STP2_447insA/insA = 0
STP2 STP2_insA447_Japn	0	Japanese, California	STP2_delA447 = 1	STP2_447delA/delA = 1
			STP2_insA447 = 0	STP2_447delA/insA = 0
				STP2_447insA/insA = 0
STP2 STP2_Asn235Thr_AfAm	0	African Americans, California	STP2_Asn235 = 0.749	STP2_235Asn/Asn = 0.562
			STP2_Thr235 = 0.251	STP2_235Asn/Thr = 0.373
				STP2_235Thr/Thr = 0.065
STP2 STP2_Asn235Thr_Cauc2	0	Caucasion, USA	STP2_Asn235 = 0.753	STP2_235Asn/Asn = 0.565
			STP2_Thr235 = 0.247	STP2_235Asn/Thr = 0.376
				STP2_235Thr/Thr = 0.059
STP2 STP2_Asn235Thr_Cauc	0	Caucasion, California	STP2_Asn235 = 0.649	STP2_235Asn/Asn = 0.42
			STP2_Thr235 = 0.351	STP2_235Asn/Thr = 0.458
				STP2_235Thr/Thr = 0.122
STP2 STP2_Asn235Thr_Chin	0	Chinese, California	STP2_Asn235 = 0.934	STP2_235Asn/Asn = 0.882
			STP2_Thr235 = 0.066	STP2_235Asn/Thr = 0.105
				STP2_235Thr/Thr = 0.013
STP2 STP2_Asn235Thr_Hisp	0	Hispanic, California	STP2_Asn235 = .623	STP2_235Asn/Asn = 0.385
			STP2_Thr235 = 0.377	STP2_235Asn/Thr = 0.476
				STP2_235Thr/Thr = 0.139
STP2 STP2_Asn235Thr_Japn	0	Japanese, California	STP2_Asn235 = 0.855	STP2_235Asn/Asn = 0.75
			STP2_Thr235 = 0.145	STP2_235Asn/Thr = 0.211
				STP2_235Thr/Thr = 0.039
STP2 STP2_Glu282Lys_AfAm	0	African Americans, California	STP2_Glu282 = 0.949	STP2_282Glu/Glu = 0.899
			STP2_Lys282 = 0.051	STP2_282Glu/Lys = 0.101
				STP2_282Lys/Lys = 0
STP2 STP2_Glu282Lys_Cauc2	0	Caucasion, USA	STP2_Glu282 = 1	STP2_282Glu/Glu = 1
			STP2_Lys282 = 0	STP2_282Glu/Lys = 0
				STP2_282Lys/Lys = 0
STP2 STP2_Glu282Lys_Cauc	0	Caucasion, California	STP2_Glu282 = 0.997	STP2_282Glu/Glu = 0.995
			STP2_Lys282 = 0.003	STP2_282Glu/Lys = 0.005
				STP2_282Lys/Lys = 0
STP2 STP2_Glu282Lys_Chin	0	Chinese, California	STP2_Glu282 = 1	STP2_282Glu/Glu = 1
			STP2_Lys282 = 0	STP2_282Glu/Lys = 0
				STP2_282Lys/Lys = 0
STP2 STP2_Glu282Lys_Hisp	0	Hispanic, California	STP2_Glu282 = 0.992	STP2_282Glu/Glu = 0.984
			STP2_Lys282 = 0.008	STP2_282Glu/Lys = 0.016
				STP2_282Lys/Lys = 0
STP2 STP2_Glu282Lys_Japn	0	Japanese, California	STP2_Glu282 = 1	STP2_282Glu/Glu = 1
			STP2_Lys282 = 0	STP2_282Glu/Lys = 0
				STP2_282Lys/Lys = 0

Each of the polymorphisms identified in this study are unique and newly described. Several of the nucleotide base changes result in amino acid changes that may alter enzyme activity by any of a number of possible mechanisms. The changes in the 5′ and 3′ UTRs may alter regulation of transcription or transcript stability. Promoter region alterations may result in altered regulation or efficiency of transcription.

All of these polymorphisms have utility. As the human genome project progresses, polymorphisms within every human gene must be identified in order to perform whole genome association studies that will be necessary for identifying genetic etiologies of complex diseases. These polymorphisms are useful for association studies.

All publications and patent applications cited in this specification are herein incorporated by reference as if each individual publication or patent application were specifically and individually indicated to be incorporated by reference. The citation of any publication is for its disclosure prior to the filing date and should not be construed as an admission that the present invention is not entitled to antedate such publication by virtue of prior invention.

Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it will be readily apparent to those of ordinary skill in the art in light of the teachings of this invention that certain changes and modifications may be made thereto without departing from the spirit or scope of the appended claims.

110 1 8396 DNA H. sapiens 1ctctccctcc ttgtctctta cctgcctgct gcctgggaca ggatgaagcg gggcccttgt 60gttgccccaa ccctggctgt tggctaagag cccacgtgat ctgcctgtga gaggagttcc 120ttccggaaga accagggcag cttctgcccc tagagggcca atgccctagc tgagtgcagt 180cccccggccc cagcctggtc cagctttggg aagagggtgc ccagttgtgc aatccaggcc 240ggggcagccg tgtcctgatc ttggtattca gggctgagcc tggagggggc ttgtgatgcc 300tgactctgtc tctctctctg gccccatgcc ttggtagctg tgaggcgtca ctgctttggg 360tgacctgatc tggctgtgat ggatgagcac gggggaaata gtggaagact cggaattaga 420agacgtgagt gggctttggc cccagcctcc ctaccccact ccctgtcctg ggctgcctgt 480gaccaacctt gtttctgcag gcacactgga tagccctgct ggagctcagt gtccctaatc 540ccctccagat actggtggcc taggggaggt catcaaagac cagtgggaca tcgacctcag 600cctgtttcca cgtttcttgt tgtttttttt tttttgtgga gacagagttt cactcttgtt 660gcccaggctg gagtgcaatg gcgtgatctt ggctcaccgc aacctctgcc tcccgggttc 720aagcgattct cctgcctcag cctcccaagt agctgggatt acaggcgtgt gccaccaggc 780ttgactaatt ttctattttt agtagagaca aggtttctcc atgttggtca ggctggtctc 840aaactcccga cttcaggtga tctgcctgcc tcggcctccc aaagtgctgg gattacagga 900gtgagccacc gtgccaggcc ttctccaggc tcttggcacc ttagccagaa acaatttaag 960gacaagtgca aaagtcatga acgtaggcag atttcctgca gagtaaaggg actcactgaa 1020gaagaggaac gtgggggtcc tcaagagagt gtctcatgcc ctacaaggtg tggggctgac 1080ctttatgggc ttcttcaact aaagaggggt atattcatga agagtccagg aaaaggtaaa 1140gatttctcaa gaccgtggtg ccacaattta cacccaaata caggtgttcc tggagccgtc 1200ttggcactgg tgggtgtacg gtttcatatg ttactgattg tacagtgaga tcctaggtga 1260aacctacatc aaatacagcg ccatgttgct tctggttggt cgcagccagc ttggtcctca 1320tcctattttt cagggactta ttggcccttg gcacatgcag ctatttcaag tttccttctt 1380ctggtcatgt gaaactgctg cctgggattt tctgttgtct tgctagcact ctattaatct 1440cacattctcg cctcttttct gtgccacccc ctgctggtcc ggctggtttt cactagagtg 1500caatacaaag tctcagtcaa gagggcctcc tgaaggttgc tgagggcagg ggtggagcta 1560gtagccggag gacctgccag tcatggggat tcctcagggg cacagaggag ggaggagggg 1620cctgtggccc tagcagggga gcagcctctc ctctgcctgg aaatcccatg cctcagtttt 1680ccccgcttgc ctctgagctc acgcaaccct gggaaggctt gggagactca cctttactca 1740gatggttgtt tacctgtctc gtgcccagct tgaccctgga ctttaaatag tgaggacaaa 1800gaacgaggag ggtgggggga tgcactcctt ccacgggggc ctgtggcttc caagcctcaa 1860cctcctctgg tctctgtctg tggagcctcc ttcaaaccca tggaaagaaa agtacctgcc 1920aggggctgtg gttcttctag gatcttctat cgatgttctg tgaggtcccc agggagccat 1980gaagctgggg ctggctccca gggcaatggg actgcagtgt ccttgttctt tcttgttcta 2040tggatccatg ctctgctcca cccctgcccc ttcactctgc ccacacgcat cactccagac 2100tggccttgtg gtcagagcct ggagtgcatg ggctgctgga ggcctgtggg ttgcactggg 2160ccaggacccc tggcaccttc aagactggcc tggagccagc aggtaggtga cctttccagg 2220gcctgcctat cccagctttc tcctccaatc cctcccctct cttgcctggg tcaattagag 2280aaagcttgtc ttttggagtt caggggcagg tcaggagccc agtgacagct caaaaaaaaa 2340accccaaaaa aaaaacccca ccattgggcc ctttcccctt tcattcttct gttttctaca 2400caccaaaccc agtcgtggct ttggagatca ctttaagctt gtctccagct ggcaaactaa 2460ggagggtaat agagaagctc ccccaccccc aaccctaccc cttccttccg gaagcaaatc 2520taagtccagc cccggctcca gatccctccc acactgacct aagaaaccct cagcacagac 2580aacacccctg cattccccac acaacaccca cactcagcca ctgcgggcga ggagggcacg 2640aggccaggtt cccaagagct caggtgagtg acacaccgga atggcccagg acgccctcac 2700cctgctcagc ttgtggctcc aacattccag aagccgaggc ctctgctatc tctgccctct 2760ccccatggat atcccatttc agacaacccc ggccggcctg aatccccctc ccttcctttt 2820tttttttccg gggaggccag gtcttgctgt caccgaggct ggagtgctgt gggatcctgg 2880ccactgcagc cttgaattcc tgggctcaag tgattctcct gcctcagtag ctaggactac 2940agaccctcac catcctgcct ggatagtttt aaaaaatatt tttaaaagat ttttagagat 3000ggggtcttcc aatgctgccc agattggtct ccaaattctg gcctcagcct ccctagggtc 3060tgggattaca ggtgggagcc accctgccca ggatcctcct tttgctgagt catcacagtt 3120ttgctcattc ccacatcagg ctctggcccc caataccagc tcagttgctc aatgggctgt 3180ttgtcctgga acccagatgg actgtggccg ggcaagtgga tcacaggcct ggccagccta 3240ggagttgcca catgtgaggg gccgaggggc tcaaggaggg gaacatcggg gagaggagcc 3300tactgggtgg aggctggggg tcccagcagg aaatggtgag acaaagggcg ctggctggca 3360ggaagacagc acaggaaggt cctagaggtt cctcagtgca gctggactct cctggagacc 3420ttcacacacc ctgacatctg ggccccgttc cacgagggtg ctttcactgg tctgcaccat 3480ggcccaggcc ctgggatttt gaacagctcc gcaggtgaat gaaaggtgag gccaggctgg 3540ggaaccacca cattagaacc cgacctggtt ttcagcccca gccccgccac tgactggcct 3600tgtgagtgcg ggcaagtcac tcaacctccc taggcctcag tgacttccct gaaagcaaga 3660attccacttt cttgctgttg tgatggtggt aagggaacgg gcctggctct ggcccctgac 3720gcaggaacat ggagctgatc caggacatct ctcgcccgcc actggagtac gtgaaggggg 3780tcccgctcat caagtacttt gcagaggcac tggggcccct gcagagcttc caggcccggc 3840ctgatgacct gctcatcagc acctacccca agtccggtag gtgaggaggg ccacccaccc 3900tctcccaggt ggcagtcccc accttggcca gcgaggtcat gctcacctca gcctgctcac 3960ctcccatctc cctccctctc caggcaccac ctgggtgagc cagattctgg acatgatcta 4020ccagggcggt gacctggaaa agtgtcaccg agctcccatc ttcatgcggg tgcccttcct 4080tgagttcaaa gtcccaggga ttccctcagg tgtgtgtgtc ctgggtgcaa ggggagtgga 4140ggaagacagg gctggggctt cagctcacca gaccttccct gacccactgc tcagggatgg 4200agactctgaa aaacacacca gccccacgac tcctgaagac acacctgccc ctggctctgc 4260tcccccagac tctgttggat cagaaggtca aggtgagact gggcacagtg gttcacaccc 4320gcaatctcag tactttggga ggctgaggtg ggaagatccc ttgaagccag aagttccaga 4380taagtctctt ccaaaaaaaa aacttagctg tgcatagtgg tgtgtgcctg taataccagt 4440tactcaggag gttgaggtgg gaggatcatc tgagcctagg agtttaaggt tacagcgagc 4500tatgatcaca ccagtgcact ccaggctggg tgacagagaa acactgtctc aaaaaacgat 4560gaatagaaag agtgtcccac cagtgcggtg gctcacacct gtaattccag cacttgaaga 4620ggctgaggca ggtggatcac ctgagactag gagtttgaga tcagcctggc caacatggca 4680aaaccccatc tctactaaaa atacaaaaaa attagccggg catggtggca ggcatctgta 4740atcccagcta cttgggaggc tgaagcagga gaattgcttg aagctgggag gcagaggttg 4800tagtcagccg agacctcacc attgcaccgc agcctgggaa acaagagcaa aactctgtct 4860caaaaaaaaa agaaaaaaat aaaaaagcgg caggtggcag ggggctgggc ctgttgtggc 4920tcacgcctgt aataccagca ctttcggagg tcgaggtggg cagatcaccc aaggttagga 4980gtttgagatc agtctggcca acatggagaa accccgtctc tactaaaaat acaaaaatta 5040gccaggcgtt ggggcaggcg ccagtaatcc cagctactcg ggaggctgag gaaggagaat 5100agcttgcacc tgggaggcgg tggttgcagt gagccgagat tgtgccactg tactccagcc 5160tgggagacac aacgagacat tgtttcaaac aaaacaaata aatattttaa aaggtttgcc 5220acctgggtgg ctcaccgctg taatgccagc attttgggag gccaagatgg gtggaccgct 5280tgagctcagg agttccagac cagcccagga aacatgggga gactccatct ctataaaaga 5340tgcaaataat cagcagggca tggtggcata gcgctatagt cccagctact caaaagtcta 5400aggttggagg attgcttgag cctgggaggt caacgttgca gtgagctatt ctcactccag 5460tgcactccaa cctgggcaac aggaaaaaag aaagcccaag gtcttttttc tcttttctct 5520tttttttgag acctagagtc ccccccccca aaaaaaaaaa aaccacaaca aaaagaaaaa 5580agcaaaggtc caggtgtggg gcatgtgaat ccagggaagg aggccccggc tcagcccagc 5640tttggtcctg ttcttctggg agagtcgcct cacttcctcc agacttgtct catcttccac 5700gggggggact gtctgccttt tgctctgatg accaaaaaca tgagactctt ccgggtagac 5760ctaagaaagg tagagggtgg gtcctcacag acccacaaaa tttggtggtg gtgggaacat 5820gcctggtgga gcatgccttg ctccagatcg gggtgtgacg cattgatgca gattatatta 5880ctatagaata tgatggtctc agggaccagg caggactttg gcttttgagc agggttcaga 5940tcctgacttg gccctacctg tgccgtgaga tctcaaacaa gtcagcctct aagcctcagc 6000ttcctccttt gccaaaccaa gagatgagct ggcctggggc aggctgtgtg gtgatggtgc 6060tggggttgag tcttctgccc ctgcaggtgg tctatgttgc ccgcaacgca aaggatgtgg 6120cggtttccta ctaccacttc taccacatgg ccaaagtgta ccctcaccct gggacctggg 6180aaagcttcct ggagaagttc atggctggag aaggtgggct tgatgggagg aaggaaggtg 6240tggagctaag gggtggtggc tacaacgcac agcaaccctg tgtcggcacc ccctgcccgc 6300ttctccagtg tcctatgggt cctggtacca gcacgtgcaa gagtggtggg agctgagccg 6360cacccaccct gttctctacc tcttctatga agacatgaag gaggtgagac cgcctttgat 6420gcttccctcc acgtgacacc tgggggcagg cacttcacag ggacctgcca aggccaccca 6480gccaccctcc ctgggcggcc cctccagcag gcccggattc cccatcctga ctccctggcc 6540caggccccac tgcagcccca tgtggcagca ggctgggcac agctctcatc tcctgtgcct 6600gagtcagctg cacgggtggc catggatcag ctactttttt ttttgagaca aaagtcttgc 6660tctgttgtcc aggatggcat gcagtggtgt gatctcagct cagtgtaacc ccccctccca 6720ggttcaagtg attctcctgc ctcagcctcc tgagtagctg agattacaga tgcacactac 6780catgcctggc taatttttgt gttgtgccat gttggccagg ttggtctcca tctcctgagc 6840tcaggtgatc cgcctgcctc agcctcccaa agtcttggga attacacgcc tgaaccacgg 6900ccccttgcca cagatcagct atctattcca attgcttctc cctgccaatg gttatgccac 6960ccagggccac aggcacggaa gaagaccatc ccagtcctta cccataggag ccaagcccag 7020ctcatgatgg gatcacaggg cagacagcaa ttcattttgc cccagggact ggggtcccag 7080gggtcgagga gctggctcta tgggttttga agtggaagtg gccagttccc ctctgaggtt 7140agagaagtgg acccctttta ttttcctgaa tcagcaatcc aagcctccac tgaggagccc 7200tctgctgctc agaaccccaa aagggagatt caaaagatcc tggagtttgt ggggcgctcc 7260ctgccagagg agactgtgga cctcatggtt gagcacacgt cgttcaagga gatgaagaag 7320aaccctatga ccaactacac caccgtccgc cgggagttca tggaccacag catctccccc 7380ttcatgagga aaggtaggtg ccggccagca cgggggtttg gagcaggtgg gagcagcagc 7440tggagcctcc ccataggcac tcggggcctc ccctgggatg agactccagc tttgctccct 7500gccttcctcc cccaggcatg gctggggact ggaagaccac cttcaccgtg gcgcagaatg 7560agcgcttcga tgcggactat gcggagaaga tggcaggctg cagcctcagc ttccgctctg 7620agctgtgaga ggggttcctg gagtcactgc agagggagtg tgcgaatcaa gcctgaccaa 7680gaggctccag aataaagtat gatttgtgtt caatgcagag tctctattcc aagccaagag 7740aaaccctgag ctgaaagagt gatcgcccac tggggccaaa tacggccacc tccccgctcc 7800agctcctcaa cttgccctgt ttggagaggg gagagggtct ggagaagtaa aacccaggag 7860acgagtagag ggggaatgtg tttaatccca gcacgtcctc tgctgtcctg ccctgtgtcg 7920ttgggggatg gcgagtctgc caggcggcat cactttttct tgggttcctt acaagccacc 7980acgtatctct gagccacatt gaggggaggg gaatagccat ctgcatagga ggtgtcttca 8040aacaggaccg agtagtcatc ctggggctgt ggggcaggca gacaggaggg gctgctcaga 8100gacccccagg ccaggacagg cacccccttc ccccagccta gaccacagga ggctctgggc 8160cgtggactct cagccactcc taacatcctt cactctgggg tcaagaagtc ttggcccagt 8220ccctgctgct acagagctct tttctcagtg gctggagacc caaggcaggg aataggcagg 8280gaggagtagg ggtgctgact cccttcctag tggggtcata gctggagggt ctgctgcctt 8340tcaaggactc tttgttgaga ggactgaggg caacccagag ggtggcaggc agggat 8396 2 1396 DNA H. sapiens CDS (426)...(1308) 2gcattcccca cacaacaccc acactcagcc actgcgggcg aggagggcac gaggccaggt 60tcccaagagc tcaggtttgt cctggaaccc agatggactg tggccgggca agtggatcac 120aggcctggcc agcctaggag ttgccacatg tgaggggccg aggggctcaa ggaggggaac 180atcggggaga ggagcctact gggtggaggc tgggggtccc agcaggaaat ggtgagacaa 240agggcgctgg ctggcaggaa gacagcacag gaaggtccta gaggttcctc agtgcagctg 300gactctcctg gagaccttca cacaccctga catctgggcc ccgttccacg agggtgcttt 360cactggtctg caccatggcc caggccctgg gattttgaac agctccgcag gtgaatgaaa 420ggaac atg gag ctg atc cag gac atc tct cgc ccg cca ctg gag tac gtg 470 Met Glu Leu Ile Gln Asp Ile Ser Arg Pro Pro Leu Glu Tyr Val 1 5 10 15aag ggg gtc ccg ctc atc aag tac ttt gca gag gca ctg ggg ccc ctg 518Lys Gly Val Pro Leu Ile Lys Tyr Phe Ala Glu Ala Leu Gly Pro Leu 20 25 30cag agc ttc cag gcc cgg cct gat gac ctg ctc atc agc acc tac ccc 566Gln Ser Phe Gln Ala Arg Pro Asp Asp Leu Leu Ile Ser Thr Tyr Pro 35 40 45aag tcc ggc acc acc tgg gtg agc cag att ctg gac atg atc tac cag 614Lys Ser Gly Thr Thr Trp Val Ser Gln Ile Leu Asp Met Ile Tyr Gln 50 55 60ggc ggt gac ctg gaa aag tgt cac cga gct ccc atc ttc atg cgg gtg 662Gly Gly Asp Leu Glu Lys Cys His Arg Ala Pro Ile Phe Met Arg Val 65 70 75ccc ttc ctt gag ttc aaa gtc cca ggg att ccc tca ggg atg gag act 710Pro Phe Leu Glu Phe Lys Val Pro Gly Ile Pro Ser Gly Met Glu Thr 80 85 90 95ctg aaa aac aca cca gcc cca cga ctc ctg aag aca cac ctg ccc ctg 758Leu Lys Asn Thr Pro Ala Pro Arg Leu Leu Lys Thr His Leu Pro Leu 100 105 110gct ctg ctc ccc cag act ctg ttg gat cag aag gtc aag gtg gtc tat 806Ala Leu Leu Pro Gln Thr Leu Leu Asp Gln Lys Val Lys Val Val Tyr 115 120 125gtt gcc cgc aac gca aag gat gtg gcg gtt tcc tac tac cac ttc tac 854Val Ala Arg Asn Ala Lys Asp Val Ala Val Ser Tyr Tyr His Phe Tyr 130 135 140cac atg gcc aaa gtg tac cct cac cct ggg acc tgg gaa agc ttc ctg 902His Met Ala Lys Val Tyr Pro His Pro Gly Thr Trp Glu Ser Phe Leu 145 150 155gag aag ttc atg gct gga gaa gtg tcc tat ggg tcc tgg tac cag cac 950Glu Lys Phe Met Ala Gly Glu Val Ser Tyr Gly Ser Trp Tyr Gln His160 165 170 175gtg caa gag tgg tgg gag ctg agc cgc acc cac cct gtt ctc tac ctc 998Val Gln Glu Trp Trp Glu Leu Ser Arg Thr His Pro Val Leu Tyr Leu 180 185 190ttc tat gaa gac atg aag gag aac ccc aaa agg gag att caa aag atc 1046Phe Tyr Glu Asp Met Lys Glu Asn Pro Lys Arg Glu Ile Gln Lys Ile 195 200 205ctg gag ttt gtg ggg cgc tcc ctg cca gag gag act gtg gac ctc atg 1094Leu Glu Phe Val Gly Arg Ser Leu Pro Glu Glu Thr Val Asp Leu Met 210 215 220gtt gag cac acg tcg ttc aag gag atg aag aag aac cct atg acc aac 1142Val Glu His Thr Ser Phe Lys Glu Met Lys Lys Asn Pro Met Thr Asn 225 230 235tac acc acc gtc cgc cgg gag ttc atg gac cac agc atc tcc ccc ttc 1190Tyr Thr Thr Val Arg Arg Glu Phe Met Asp His Ser Ile Ser Pro Phe240 245 250 255atg agg aaa ggc atg gct ggg gac tgg aag acc acc ttc acc gtg gcg 1238Met Arg Lys Gly Met Ala Gly Asp Trp Lys Thr Thr Phe Thr Val Ala 260 265 270cag aat gag cgc ttc gat gcg gac tat gcg gag aag atg gca ggc tgc 1286Gln Asn Glu Arg Phe Asp Ala Asp Tyr Ala Glu Lys Met Ala Gly Cys 275 280 285agc ctc agc ttc cgc tct gag c tgtgagaggg gttcctggag tcactgcaga 1338Ser Leu Ser Phe Arg Ser Glu 290gggagtgtgc gaatcaagcc tgaccaagag gctccagaat aaagtatgat ttgtgttc 1396 3 295 PRT H. sapiens 3Met Glu Leu Ile Gln Asp Ile Ser Arg Pro Pro Leu Glu Tyr Val Lys 1 5 10 15Gly Val Pro Leu Ile Lys Tyr Phe Ala Glu Ala Leu Gly Pro Leu Gln 20 25 30Ser Phe Gln Ala Arg Pro Asp Asp Leu Leu Ile Ser Thr Tyr Pro Lys 35 40 45Ser Gly Thr Thr Trp Val Ser Gln Ile Leu Asp Met Ile Tyr Gln Gly 50 55 60Gly Asp Leu Glu Lys Cys His Arg Ala Pro Ile Phe Met Arg Val Pro65 70 75 80Phe Leu Glu Phe Lys Val Pro Gly Ile Pro Ser Gly Met Glu Thr Leu 85 90 95Lys Asn Thr Pro Ala Pro Arg Leu Leu Lys Thr His Leu Pro Leu Ala 100 105 110Leu Leu Pro Gln Thr Leu Leu Asp Gln Lys Val Lys Val Val Tyr Val 115 120 125Ala Arg Asn Ala Lys Asp Val Ala Val Ser Tyr Tyr His Phe Tyr His 130 135 140Met Ala Lys Val Tyr Pro His Pro Gly Thr Trp Glu Ser Phe Leu Glu145 150 155 160Lys Phe Met Ala Gly Glu Val Ser Tyr Gly Ser Trp Tyr Gln His Val 165 170 175Gln Glu Trp Trp Glu Leu Ser Arg Thr His Pro Val Leu Tyr Leu Phe 180 185 190Tyr Glu Asp Met Lys Glu Asn Pro Lys Arg Glu Ile Gln Lys Ile Leu 195 200 205Glu Phe Val Gly Arg Ser Leu Pro Glu Glu Thr Val Asp Leu Met Val 210 215 220Glu His Thr Ser Phe Lys Glu Met Lys Lys Asn Pro Met Thr Asn Tyr225 230 235 240Thr Thr Val Arg Arg Glu Phe Met Asp His Ser Ile Ser Pro Phe Met 245 250 255Arg Lys Gly Met Ala Gly Asp Trp Lys Thr Thr Phe Thr Val Ala Gln 260 265 270Asn Glu Arg Phe Asp Ala Asp Tyr Ala Glu Lys Met Ala Gly Cys Ser 275 280 285Leu Ser Phe Arg Ser Glu Leu 290 295 4 18 DNA H. sapiens 4cccaaataca ggtgttcc 18 5 17 DNA H. sapiens 5ggagcagagc aaggatc 17 6 21 DNA H. sapiens 6ttcttctagg atcttctatc g 21 7 18 DNA H. sapiens 7actcagcaaa aggaggat 18 8 18 DNA H. sapiens 8ttagagatgg ggtcttcc 18 9 15 DNA H. sapiens 9gggcgagaga tgtcc 15 10 17 DNA H. sapiens 10ggagaggagc ctactgg 17 11 16 DNA H. sapiens 11agtctgaggt gagcat 16 12 17 DNA H. sapiens 12gcctcagtga cttccct 17 13 20 DNA H. sapiens 13tttggaagag acttatctgg 20 14 16 DNA H. sapiens 14gcaggacttt ggcttt 16 15 16 DNA H. sapiens 15gactcaggca caggag 16 16 16 DNA H. sapiens 16gaccatccca gtcctt 16 17 15 DNA H. sapiens 17ccccaacgac acagg 15 18 15 DNA H. sapiens 18tggagcccgt cttgg 15 19 18 DNA H. sapiens 19cagcagtttc acttgacc 18 20 14 DNA H. sapiens 20tgccaccccc tgct 14 21 14 DNA H. sapiens 21aggctgctcc cctg 14 22 14 DNA H. sapiens 22gggctcacgc aacc 14 23 19 DNA H. sapiens 23gcaggtactt ttctttcca 19 24 21 DNA H. sapiens 24ttcttctagg atcttctatc g 21 25 18 DNA H. sapiens 25tttttgaggt gtcactgg 18 26 16 DNA H. sapiens 26cccacacaac acccac 16 27 16 DNA H. sapiens 27gcttctggaa tgttgg 16 28 19 DNA H. sapiens 28cggaaaaaaa aaaaggaag 19 29 14 DNA H. sapiens 29caatgctgcc caga 14 30 17 DNA H. sapiens 30gctccactga ggaacct 17 31 17 DNA H. sapiens 31ggagaggagc ctactgg 17 32 18 DNA H. sapiens 32taccaccatc acaacagc 18 33 19 DNA H. sapiens 33ctgaaagcaa gaaatccac 19 34 16 DNA H. sapiens 34aggctgaggt gagcat 16 35 14 DNA H. sapiens 35gcggtgacct ggaa 14 36 20 DNA H. sapiens 36tttggaagag acttatctgg 20 37 17 DNA H. sapiens 37ctgacttgcc cctacct 17 38 16 DNA H. sapiens 38tagccaccac ccctta 16 39 18 DNA H. sapiens 39ccaaagtgta ccctcacc 18 40 14 DNA H. sapiens 40agcctgctgc caca 14 41 16 DNA H. sapiens 41gaccatccca gtcctt 16 42 14 DNA H. sapiens 42caaacccccg tgct 14 43 18 DNA H. sapiens 43ctgtggacct cttggttg 18 44 22 DNA H. sapiens 44cacaaatcat actttattct gg 22 45 15 DNA H. sapiens 45cgatgcggac tatgc 15 46 15 DNA H. sapiens 46ccccaacgac acagg 15 47 22 DNA H. sapiens 47ggtgctgggg ttgagtcttc tg 22 48 27 DNA H. sapiens 48caaaggatgt ggcggtttcc tactacc 27 49 23 DNA H. sapiens 49acaccttcct tcctcccatc aag 23 50 28 DNA H. sapiens 50cgcaaaggat gtggtggttt cctactac 28 51 24 DNA H. sapiens 51ggagactgtg gacctcatgg ttga 24 52 32 DNA H. sapiens 52tagttggtca tagggttctt cttcatctcc tt 32 53 21 DNA H. sapiens 53ccggcaccta cctttcctca t 21 54 30 DNA H. sapiens 54tagttggtca taggggtctt cttcatctcc 30 55 21 DNA H. sapiens 55agctttgctc cctgccttcc t 21 56 24 DNA H. sapiens 56ctgccatctt ctccgcatag tccg 24 57 22 DNA H. sapiens 57ggaacccctc tcacagctca ga 22 58 24 DNA H. sapiens 58tgccatcttc ttcgcatagt ccgc 24 59 22 DNA H. sapiens 59ggtgctgggg ttgagtcttc tg 22 60 25 DNA H. sapiens 60atggccaaag tgtaccctca ccctg 25 61 23 DNA H. sapiens 61acaccttcct tcctcccatc aag 23 62 25 DNA H. sapiens 62catggccaaa gtgtaaccct caccc 25 63 21 DNA H. sapiens 63ccagctcctc aacttgccct g 21 64 21 DNA H. sapiens 64ccagctcctc tacttgccct g 21 65 21 DNA H. sapiens 65gtgagagggg ttcctggagt c 21 66 21 DNA H. sapiens 66gtgagagggg ctcctggagt c 21 67 21 DNA H. sapiens 67catgaagctg gggctggctc c 21 68 21 DNA H. sapiens 68catgaagctg aggctggctc c 21 69 21 DNA H. sapiens 69ctcgtgccca ggttgaccct g 21 70 21 DNA H. sapiens 70ctcgtgccca agttgaccct g 21 71 21 DNA H. sapiens 71gggattcctc aggggcacag a 21 72 21 DNA H. sapiens 72gggattcctc cggggcacag a 21 73 21 DNA H. sapiens 73acagcgccat gttgcttctg g 21 74 21 DNA H. sapiens 74acagcgccat attgcttctg g 21 75 21 DNA H. sapiens 75cagccactgc gggcgaggag g 21 76 21 DNA H. sapiens 76cagccactgc aggcgaggag g 21 77 21 DNA H. sapiens 77aggagggcac aaggccaggt t 21 78 21 DNA H. sapiens 78aggagggcac gaggccaggt t 21 79 21 DNA H. sapiens 79ggggaacatc ggggagagga g 21 80 21 DNA H. sapiens 80ggggaacatc agggagagga g 21 81 20 DNA H. sapiens 81ccaaagtgta ccctcaccct 20 82 21 DNA H. sapiens 82ccaaagtgta accctcaccc t 21 83 20 DNA H. sapiens 83aaggatgtgg ggtttcctac 20 84 20 DNA H. sapiens 84aaggatgtgg ggtttcctac 20 85 20 DNA H. sapiens 85atgaagaaga ccctatgacc 20 86 20 DNA H. sapiens 86atgaagaaga ccctatgacc 20 87 20 DNA H. sapiens 87ggactatgcg agaagatggc 20 88 20 DNA H. sapiens 88ggactatgcg agaagatggc 20 89 21 DNA H. sapiens 89aagggggtcc cgctcatcaa g 21 90 21 DNA H. sapiens 90aagggggtcc tgctcatcaa g 21 91 21 DNA H. sapiens 91ctctgctatc tctgccctct c 21 92 21 DNA H. sapiens 92ctctgctatc cctgccctct c 21 93 21 DNA H. sapiens 93ctctcccagg tggcagtccc c 21 94 21 DNA H. sapiens 94ctctcccagg cggcagtccc c 21 95 20 DNA H. sapiens 95cctttgccaa ccaagagatg 20 96 19 DNA H. sapiens 96cctttgccac caagagatg 19 97 21 DNA H. sapiens 97gtgtcggcac tccctgcccg c 21 98 21 DNA H. sapiens 98gtgtcggcac cccctgcccg c 21 99 21 DNA H. sapiens 99cctccctggg cggcccctcc a 21 100 21 DNA H. sapiens 100cctccctggg tggcccctcc a 21 101 21 DNA H. sapiens 101ttgttctatg gatccatgct c 21 102 21 DNA H. sapiens 102ttgttctatg catccatgct c 21 103 21 DNA H. sapiens 103catgggctgc tggaggcctg t 21 104 21 DNA H. sapiens 104catgggctgc cggaggcctg t 21 105 21 DNA H. sapiens 105actgggccag gacccctggc a 21 106 21 DNA H. sapiens 106actgggccag aacccctggc a 21 107 21 DNA H. sapiens 107cctgcctatc ccagctttct c 21 108 21 DNA H. sapiens 108cctgcctatc tcagctttct c 21 109 21 DNA H. sapiens 109gcctatccca tctttctcct c 21 110 21 DNA H. sapiens 110gcctatccca gctttctcct c 21

Claims

1. An isolated STP2 polynucleotide comprising a nucleic acid sequence selected from the group consisting of:(a) a nucleic acid sequence comprising at least 12 contiguous nucleotides of a nucleic acid sequence selected from the group consisting of SEQ ID NO:68, SEQ ID NO:70, SEQ ID NO:72, SEQ ID NO:74, SEQ ID NO:76, SEQ ID NO:77, SEQ ID NO:82, SEQ ID NO:84, SEQ ID NO:88, SEQ ID NO:96, SEQ D NO:97, SEQ ID NO:100, SEQ ID NO:102, SEQ ID NO:104, SEQ ID NO:108, and SEQ ID NO:109, (b) a nucleic acid sequence comprising at least 50 contiguous nucleotides and comprising a nucleic acid sequence selected from the group consisting of SEQ ID NO:80, and SEQ ID NO:106; (c) a nucleic acid sequence comprising at least 100 contiguous nucleotides and comprising a nucleic acid sequence of SEQ ID NO:102; and, (d) a nucleic acid sequence that is fully complementary to a nucleic acid sequence of (a), (b), or (c).

2. An isolated STP2 polynucleotide according to claim 1, wherein the polynucleotide is a nucleic acid probe for the detection of STP2 locus polymorphisms.

3. An isolated STP2 polynucleotide according to claim 2, wherein said polynucleotide is conjugated to a detectable marker.

4. An array of polynucleotides comprising:two or more isolated polynucleotides comprising at least one STP2 polynucleotide of claim 1.

5. A method for detecting in an individual a STP2 polynucleotide, the method comprising:(a) obtaining a nucleic acid sample that has been isolated from an individual; and (b) contacting said nucleic acid sample with a STP2 polynucleotide probe, wherein said STP2 polynucleotide probe comprises a nucleic acid sequence selected from the group consisting (i) a nucleic acid sequence comprising at least 12 contiguous nucleotides of a nucleic acid sequence selected from the group consisting of SEQ ID NO:68, SEQ ID NO:70, SEQ D) NO:72, SEQ ID NO:74, SEQ ID NO:76, SEQ ID NO:77, SEQ ID NO:82, SEQ ID NO:84, SEQ ID NO:88, SEQ ID NO:96, SEQ ID NO:97, SEQ ID NO:100, SEQ ID NO:102, SEQ ID NO:104, SEQ ID NO:108, and SEQ ID NO:109; (ii) a nucleic acid sequence comprising at least 50 contiguous nucleotides and comprising a nucleic acid sequence selected from the group consisting of SEQ ID NO:80, and SEQ ID NO:106; (iii) a nucleic acid sequence comprising at least 100 contiguous nucleotides and comprising a nucleic acid sequence of SEQ ID NO:102; and, (iv) a nucleic acid sequence that is fully complementary to a nucleic acid sequence of (i)-(iii); and, (c) detecting specific hybridization between said polynucleotide probe and said nucleic acid sample as indicative of the presence of a STP2 polynucleotide in said nucleic acid sample.

6. A method according to claim 5, wherein said detecting step comprises detecting hybridization between sad nucleic acid sample with an array of polynucleotides comprising:two or more isolated polynucleotides comprising at least one STP2 polynucleotide probe of claim 5.