Entity Details

Primary name RGR_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP47804
EntryNameRGR_HUMAN
FullNameRPE-retinal G protein-coupled receptor
TaxID9606
Evidenceevidence at protein level
Length291
SequenceStatuscomplete
DateCreated1996-02-01
DateModified2021-06-02

Ontological Relatives

GenesRGR

GO terms

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GOName
GO:0001750 photoreceptor outer segment
GO:0004930 G protein-coupled receptor activity
GO:0005887 integral component of plasma membrane
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:0071482 cellular response to light stimulus

Subcellular Location

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Subcellular Location
Membrane

Domains

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DomainNameCategoryType
IPR000276 G protein-coupled receptor, rhodopsin-likeFamilyFamily
IPR001793 Retinal pigment epithelium GPCRFamilyFamily
IPR017452 GPCR, rhodopsin-like, 7TMDomainDomain
IPR027430 Visual pigments (opsins) retinal binding siteSiteBinding site

Diseases

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Disease IDSourceNameDescription
613769 OMIMRetinitis pigmentosa 44 (RP44)A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. The disease is caused by variants affecting the gene represented in this entry.