Reference Gene

Gene name Alias Species Exons Type Paralogs EC number OMIM
RGR retinal G protein coupled receptor RP44 Homo sapiens 7 protein-coding RASGRP1 , RASGRP4 , RASGRP2 , RASGRP3 , RGL3 , RALGDS , RGL1 , RALGPS1 , RALGPS2 , RASGEF1C , RASGEF1A , RASGEF1B , RAPGEF3 , RAPGEFL1 , RAPGEF5 , RAPGEF4 , RAPGEF1 , SOS2 , SOS1 , RAPGEF2 , RAPGEF6 , RASGRF1 , RASGRF2 , RGR , RGR , RGR , RGR , RGR , RGR , RGR , RGR , RGR , RGR , RGR , RGR , RGR , RASGRP1 , RASGRP4 , RASGRP2 , RASGRP3 , RGL3 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , RGL4 , GPR88 , RRH , OPN4 , OPN5 , RHO , OPN1MW2 , OPN1MW3 , OPN1MW , OPN1LW , OPN1SW , OPN1SW , OPN3 , GPR52 600342

Summary

This gene encodes a putative retinal G-protein coupled receptor. The gene is a member of the opsin subfamily of the 7 transmembrane, G-protein coupled receptor 1 family. Like other opsins which bind retinaldehyde, it contains a conserved lysine residue in the seventh transmembrane domain. The protein acts as a photoisomerase to catalyze the conversion of all-trans-retinal to 11-cis-retinal. The reverse isomerization occurs with rhodopsin in retinal photoreceptor cells. The protein is exclusively expressed in tissue adjacent to retinal photoreceptor cells, the retinal pigment epithelium and Mueller cells. This gene may be associated with autosomal recessive and autosomal dominant retinitis pigmentosa (arRP and adRP, respectively). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

GeneOntology

Gene Loss events - RGR (2 results)

GL_ID Species Order Gene Loss Mechanism Loss Type Lineage Specific Citation
GL_PSQECC Chrysochloris asiatica Afrosoricida LOF (frameshift, premature stop, ss) Full No 10.1093/icb/icy004
GL_RTUJFA Miniopterus natalensis Chiroptera Gene deletion Full No 10.1093/icb/icy004