Homo sapiens Protein: RGS9 | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-383535.5 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | RGS9 | ||||||||||||||||||||||
Protein Name | regulator of G-protein signaling 9 | ||||||||||||||||||||||
Synonyms | PERRS; RGS9L; | ||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Protein | ENSP00000396329 | ||||||||||||||||||||||
InnateDB Gene | IDBG-65027 (RGS9) | ||||||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||||||
Function | Inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits thereby driving them into their inactive GDP-bound form. Binds to G(t)-alpha. Involved in phototransduction; key element in the recovery phase of visual transduction (By similarity). {ECO:0000250}. | ||||||||||||||||||||||
Subcellular Localization | Isoform 3: Membrane; Peripheral membrane protein. Note=Isoform 3 is targeted to the membrane via its interaction with RGS9BP. {ECO:0000250}. | ||||||||||||||||||||||
Disease Associations | Prolonged electroretinal response suppression (PERRS) [MIM:608415]: Characterized by difficulty adjusting to sudden changes in luminance levels mediated by cones. {ECO:0000269PubMed:14702087}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||||||
Tissue Specificity | Highly expressed in the caudate and putamen, lower levels found in the hypothalamus and nucleus accumbens and very low levels in cerebellum. Not expressed in globus pallidus or cingulate cortex. Isoform 2 is expressed predominantly in pineal gland and retina. Isoform 3 is expressed in retina (abundant in photoreceptors). | ||||||||||||||||||||||
Comments | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 10 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||||||
PDB ID | |||||||||||||||||||||||
InterPro |
IPR000342
Regulator of G protein signalling domain IPR000591 DEP domain IPR015898 G-protein gamma-like domain IPR016137 Regulator of G protein signalling superfamily |
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PFAM |
PF00615
PF00610 PF00631 |
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PRINTS |
PR01301
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PIRSF | |||||||||||||||||||||||
SMART |
SM00049
SM00224 SM00315 |
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TIGRFAMs | |||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||
Modification | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | O75916 | ||||||||||||||||||||||
PhosphoSite | PhosphoSite-O75916 | ||||||||||||||||||||||
TrEMBL | |||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 8787 | ||||||||||||||||||||||
UniGene | Hs.664380 | ||||||||||||||||||||||
RefSeq | NP_001075424 | ||||||||||||||||||||||
HUGO | HGNC:10004 | ||||||||||||||||||||||
OMIM | 604067 | ||||||||||||||||||||||
CCDS | CCDS45764 | ||||||||||||||||||||||
HPRD | 04962 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AC015821 AC060771 AF071476 AF073710 AF178056 AF178057 AF178058 AF178059 AF178060 AF178061 AF178062 AF178063 AF178064 AF178065 AF178066 AF178067 AF178068 AF178069 AF178070 AF178071 AF178072 AF493932 AF493933 AK290535 AY585190 AY585191 CH471099 | ||||||||||||||||||||||
GenPept | AAC25430 AAC64040 AAG09311 AAG09312 AAM12646 AAM12647 AAT79493 AAT79494 BAF83224 EAW88998 | ||||||||||||||||||||||