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Ovarian Kaleidoscope Database (OKdb)

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Hsueh lab

HPMR

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since 01/2001:
176557

SNP 13429458 OKDB#: 4642
 Symbols: Species: human
 Synonyms:  Locus:


For retrieval of Nucleotide and Amino Acid sequences please go to:
R-L INTERACTIONS   MGI

DNA Microarrays
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link to BioGPS
General Comment
General function
Comment
Cellular localization
Comment
Ovarian function
Comment
Expression regulated by
Comment
Ovarian localization
Comment
Follicle stages
Comment
Phenotypes PCO (polycystic ovarian syndrome)
Mutations 1 mutations

Species: human
Mutation name: None
type: naturally occurring
fertility: subfertile
Comment: Family-based analysis of susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3. Zhao H et al. Polycystic ovary syndrome (PCOS) is a complex endocrine-metabolic disorder. A previous genome-wide association study (GWAS) identified five single nucleotide polymorphisms (SNPs) which were independently associated with PCOS in Han Chinese. To overcome population strati?cation, a family-based analysis was conducted to validate whether these five SNPs are associated with PCOS.

SNPs
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http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=13429458
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created: March 11, 2012, 11:26 a.m. by: hsueh   email:
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last update: March 11, 2012, 11:26 a.m. by: hsueh    email:



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