Homo sapiens Gene: PRDM9
Summary
InnateDB Gene IDBG-13910.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PRDM9
Gene Name PR domain containing 9
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000164256
Encoded Proteins
PR domain containing 9
PR domain containing 9
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The PR domain is a protein-protein interaction module of about 100 amino acids. PR domain-containing proteins, such as PRDM9, are often involved in transcriptional regulation (Jiang and Huang, 2000 [PubMed 10668202]).[supplied by OMIM, Mar 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 5:23507155-23528597
Strand Forward strand
Band p14.2
Transcripts
ENST00000296682 ENSP00000296682
ENST00000502755 ENSP00000425471
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003676 nucleic acid binding
GO:0005515 protein binding
GO:0010844 recombination hotspot binding
GO:0042800 histone methyltransferase activity (H3-K4 specific)
GO:0043565 sequence-specific DNA binding
GO:0046872 metal ion binding
Biological Process
GO:0006311 meiotic gene conversion
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0007283 spermatogenesis
GO:0010845 positive regulation of reciprocal meiotic recombination
GO:0016571 histone methylation
GO:0034968 histone lysine methylation
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0051568 histone H3-K4 methylation
GO:0060903 positive regulation of meiosis I
Cellular Component
GO:0005622 intracellular
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005694 chromosome
Orthologs
Species
Mus musculus
Gene ID
Gene Order
Pathways
NETPATH
REACTOME
Meiotic recombination pathway
Cell Cycle pathway
Meiosis pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL D6RD68
UniProt Splice Variant
Entrez Gene 56979
UniGene Hs.283096
RefSeq NM_020227
HUGO HGNC:13994
OMIM 609760
CCDS CCDS43307
HPRD 17905
IMGT
EMBL AC025451
GenPept
RNA Seq Atlas 56979