PRDM9 Chromosome 5

PR/SET domain 9
3 variants 3 Health Risk

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What This Gene Does
The protein encoded by this gene is a zinc finger protein with histone methyltransferase activity that catalyzes histone H3 lysine 4 trimethylation (H3K4me3) during meiotic prophase. This protein contains multiple domains, including a Kruppel-associated box (KRAB) domain, an SSX repression domain (SSXRD), a PRD1-BF1 and RIZ homologous region, a subclass of SET (PR/SET) domain, and a tandem array of C2H2 zinc fingers. The zinc finger array recognizes a short sequence motif, leading to local H3K4me3, and meiotic recombination hotspot activity. The observed allelic variation alters the DNA-binding sequence specificity of the protein, resulting in distinct meiotic recombination hotspots amongst individuals and populations. Multiple alternate alleles of this gene have been described. [provided by RefSeq, Jul 2015]
Gene Info
Gene Group
"Zinc fingers C2H2-type|Histone lysine methyltransferases|PR/SET domain family|KRAB domain containing"
Locus Type
gene with protein product
Location
5p14.2
Ensembl
ENSG00000164256
Associated Conditions (1)
Genetic non-acquired premature ovarian failure
Key Variants
All Variants (3)
RSID Category Clinical Significance Conditions
RS201284800 Health Risk Pathogenic Genetic non-acquired premature ovarian failure, Genetic non-acquired premature ovarian failure
RS2126427825 Health Risk Pathogenic Genetic non-acquired premature ovarian failure, Genetic non-acquired premature ovarian failure
RS747527740 Health Risk Pathogenic Genetic non-acquired premature ovarian failure, Genetic non-acquired premature ovarian failure
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