Entity Details

Primary name TRPM1
Entity type gene
Source Source Link

Details

PrimaryID4308
RefseqGeneNG_016453
SymbolTRPM1
Nametransient receptor potential cation channel subfamily M member 1
Chromosome15
Location15q13.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-11-10
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsTRPM1_HUMAN

GO terms

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GOName
GO:0005261 cation channel activity
GO:0005262 calcium channel activity
GO:0005789 endoplasmic reticulum membrane
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0007216 G protein-coupled glutamate receptor signaling pathway
GO:0007601 visual perception
GO:0030424 axon
GO:0051262 protein tetramerization
GO:0060402 calcium ion transport into cytosol
GO:0070588 calcium ion transmembrane transport
GO:0071482 cellular response to light stimulus
GO:0098655 cation transmembrane transport

Diseases

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Disease IDSourceNameDescription
613216 OMIMNight blindness, congenital stationary, 1C (CSNB1C)A non-progressive retinal disorder characterized by impaired night vision, often associated with nystagmus and myopia. The disease is caused by variants affecting the gene represented in this entry.

Interactions

9 interactions

InteractorPartnerSourcesPublicationsLink
TRPM1FXR1BioGRID, IntAct32296183 details
TRPM1TRPM1BioGRID, HPRD11535825 details
TRPM1MYCIntAct21150319 details
TRPM1H2BC9BioGRID, IntAct30021884 details
TRPM1H3-4BioGRID, IntAct30021884 details
TRPM1BCORBioGRID26687479 details
TRPM1NANOGBioGRID26687479 details
TRPM1POU5F1BioGRID26687479 details
TRPM1TP53BioGRID32807901 details