Entity Details

Primary name OPN1SW
Entity type gene
Source Source Link

Details

PrimaryID611
RefseqGeneNG_009094
SymbolOPN1SW
Nameopsin 1, short wave sensitive
Chromosome7
Location7q32.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-01-22
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsOPSB_HUMAN

GO terms

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GOName
GO:0001523 retinoid metabolic process
GO:0001750 photoreceptor outer segment
GO:0001917 photoreceptor inner segment
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0007165 signal transduction
GO:0007186 G protein-coupled receptor signaling pathway
GO:0007601 visual perception
GO:0007602 phototransduction
GO:0008020 G protein-coupled photoreceptor activity
GO:0018298 protein-chromophore linkage
GO:0038023 signaling receptor activity
GO:0048471 perinuclear region of cytoplasm
GO:0071482 cellular response to light stimulus
GO:0071492 cellular response to UV-A
GO:0097381 photoreceptor disc membrane

Diseases

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Disease IDSourceNameDescription
190900 OMIMTritan color blindness (CBT)A disorder of vision characterized by a selective deficiency of blue spectral sensitivity. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
OPN1SWMFFBioGRID, IntAct32296183 details