Entity Details

Primary name CATSPER2
Entity type gene
Source Source Link

Details

PrimaryID117155
RefseqGeneNG_009283
SymbolCATSPER2
Namecation channel sperm associated 2
Chromosome15
Location15q15.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-11-04
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCTSR2_HUMAN

GO terms

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GOName
GO:0005227 calcium activated cation channel activity
GO:0005244 voltage-gated ion channel activity
GO:0005262 calcium channel activity
GO:0005886 plasma membrane
GO:0007275 multicellular organism development
GO:0009566 fertilization
GO:0030317 flagellated sperm motility
GO:0031514 motile cilium
GO:0032570 response to progesterone
GO:0034765 regulation of ion transmembrane transport
GO:0035036 sperm-egg recognition
GO:0036128 CatSper complex
GO:0048240 sperm capacitation

Diseases

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Disease IDSourceNameDescription
611102 OMIMDeafness-infertility syndrome (DIS)Characterized by deafness and infertility and is caused by large contiguous gene deletions at 15q15.3 that removes both STRC and CATSPER2 genes. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
CATSPER2CACNA1IIntAct16740636 details