Reference Gene

Gene name Alias Species Exons Type Paralogs EC number OMIM
RGS9BP regulator of G protein signaling 9 binding protein R9AP , RGS9 , PERRS , PERRS2 Homo sapiens 1 protein-coding 607814

Summary

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. [provided by RefSeq, Mar 2010]

GeneOntology

Gene Loss events - RGS9BP (1 results)

GL_ID Species Order Gene Loss Mechanism Loss Type Lineage Specific Citation
GL_ON0DME Carlito syrichta Primates Gene deletion Full No 10.1093/icb/icy004