Entity Details

Primary name GRK1
Entity type gene
Source Source Link

Details

PrimaryID6011
RefseqGene
SymbolGRK1
NameG protein-coupled receptor kinase 1
Chromosome13
Location13q34
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-08-18
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsGRK1_HUMAN

GO terms

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GOName
GO:0004672 protein kinase activity
GO:0004703 G protein-coupled receptor kinase activity
GO:0005524 ATP binding
GO:0007601 visual perception
GO:0008277 regulation of G protein-coupled receptor signaling pathway
GO:0016056 rhodopsin mediated signaling pathway
GO:0022400 regulation of rhodopsin mediated signaling pathway
GO:0046777 protein autophosphorylation
GO:0050254 rhodopsin kinase activity
GO:0097381 photoreceptor disc membrane

Diseases

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Disease IDSourceNameDescription
613411 OMIMNight blindness, congenital stationary, Oguchi type 2 (CSNBO2)A non-progressive retinal disorder characterized by impaired night vision, often associated with nystagmus and myopia. Congenital stationary night blindness Oguchi type is associated with fundus discoloration and abnormally slow dark adaptation. The disease is caused by variants affecting the gene represented in this entry.

Interactions

11 interactions