Entity Details

Primary name RGS9_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO75916
EntryNameRGS9_HUMAN
FullNameRegulator of G-protein signaling 9
TaxID9606
Evidenceevidence at transcript level
Length674
SequenceStatuscomplete
DateCreated2000-05-30
DateModified2021-06-02

Ontological Relatives

GenesRGS9

GO terms

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GOName
GO:0001975 response to amphetamine
GO:0005096 GTPase activator activity
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005886 plasma membrane
GO:0006457 protein folding
GO:0007186 G protein-coupled receptor signaling pathway
GO:0007212 dopamine receptor signaling pathway
GO:0007399 nervous system development
GO:0007601 visual perception
GO:0008277 regulation of G protein-coupled receptor signaling pathway
GO:0009968 negative regulation of signal transduction
GO:0032355 response to estradiol
GO:0035556 intracellular signal transduction
GO:0098839 postsynaptic density membrane
GO:0098978 glutamatergic synapse
GO:1904783 positive regulation of NMDA glutamate receptor activity
GO:1905912 regulation of calcium ion export across plasma membrane

Subcellular Location

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Subcellular Location
Membrane

Domains

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DomainNameCategoryType
IPR000591 DEP domainDomainDomain
IPR015898 G-protein gamma-like domainDomainDomain
IPR016137 RGS domainDomainDomain
IPR036284 G-protein gamma-like domain superfamilyFamilyHomologous superfamily
IPR036305 RGS domain superfamilyFamilyHomologous superfamily
IPR036388 Winged helix-like DNA-binding domain superfamilyFamilyHomologous superfamily
IPR036390 Winged helix DNA-binding domain superfamilyFamilyHomologous superfamily
IPR040759 Regulator of G-protein signalling, DHEX domainDomainDomain

Diseases

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Disease IDSourceNameDescription
608415 OMIMProlonged electroretinal response suppression (PERRS)Characterized by difficulty adjusting to sudden changes in luminance levels mediated by cones. The disease is caused by variants affecting the gene represented in this entry.