RGS9

This gene encodes a member of the RGS family of GTPase activating proteins that function in various signaling pathways by accelerating the deactivation of G proteins. This protein is anchored to photoreceptor membranes in retinal cells and deactivates G proteins in the rod and cone phototransduction cascades. Mutations in this gene result in bradyopsia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

Description

regulator of G protein signaling 9

Protein family

Disease related genes, Mapped to neXtProt, Mapped to UniProt SWISS-PROT, Plasma proteins, Predicted intracellular proteins, Protein evidence (Peptideatlas)

Chromosome

17:q24.1 (65100812 - 65227703)

Ensembl ID

ENSG00000108370  (ver. 99.38)

Orthologs

Mouse Rgs9: ENSMUSG00000020599

UniProt

O75916

neXtProt

NX_O75916

Human splice variants
Mouse splice variants