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RGS9BP

From Wikipedia, the free encyclopedia
RGS9BP
Identifiers
AliasesRGS9BP, regulator of G protein signaling 9 binding protein, PERRS, R9AP, RGS9, regulator of G-protein signaling 9 binding protein
External IDsOMIM: 607814; MGI: 2384418; HomoloGene: 17113; GeneCards: RGS9BP; OMA:RGS9BP - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_207391

NM_145840

RefSeq (protein)

NP_997274

NP_665839

Location (UCSC)Chr 19: 32.68 – 32.68 MbChr 7: 35.28 – 35.29 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Regulator of G protein signaling 9 binding protein is a protein that in humans is encoded by the RGS9BP gene. [5]

Function

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The protein encoded by this gene functions as a regulator of G protein-coupled receptor signaling in phototransduction. Studies in bovine and mouse show that this gene is expressed only in the retina, and is localized in the rod outer segment membranes. This protein is associated with a heterotetrameric complex, specifically interacting with the regulator of G-protein signaling 9, and appears to function as the membrane anchor for the other largely soluble interacting partners. Mutations in this gene are associated with prolonged electroretinal response suppression (PERRS), also known as bradyopsia.

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000186326Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000056043Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: Regulator of G protein signaling 9 binding protein". Retrieved 2017-05-19.

Further reading

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This article incorporates text from the United States National Library of Medicine, which is in the public domain.