Entity Details

Primary name ARR3
Entity type gene
Source Source Link

Details

PrimaryID407
RefseqGeneNG_050734
SymbolARR3
Namearrestin 3
ChromosomeX
LocationXq13.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-07-29
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsARRC_HUMAN

GO terms

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GOName
GO:0001664 G protein-coupled receptor binding
GO:0001750 photoreceptor outer segment
GO:0001917 photoreceptor inner segment
GO:0001932 regulation of protein phosphorylation
GO:0002031 G protein-coupled receptor internalization
GO:0002046 opsin binding
GO:0005737 cytoplasm
GO:0007165 signal transduction
GO:0007601 visual perception
GO:0045202 synapse
GO:0051219 phosphoprotein binding

Diseases

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Disease IDSourceNameDescription
301010 OMIMMyopia 26, X-linked, female-limited (MYP26)A form of myopia, a refractive error of the eye, in which parallel rays from a distant object come to focus in front of the retina, vision being better for near objects than for far. MYP26 is characterized by typical tigroid fundus changes commonly seen in early onset high myopia, and an unusual pattern of X-linked female-limited inheritance. The disease may be caused by variants affecting the gene represented in this entry.