RPE-retinal G protein-coupled receptor (RGR)
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Function
- receptor for all-trans-retinal & 11-cis-retinal
- preferentially binds all-trans-retinal
- may catalyze the isomerization of the retinal by a retinochrome-like mechanism
- covalently binds all-trans-retinal & 11-cis-retinal
Structure
- belongs to the G-protein coupled receptor 1 family Opsin subfamily
Compartment
membrane
Alternative splicing
named isoforms=3
Expression
- preferentially expressed at high levels in the retinal pigment epithelium (RPE) & Mueller cells of the neural retina
Pathology
- defects in RGR are a cause of retinitis pigmentosa
More general terms
References
- ↑ UniProt http://www.uniprot.org/uniprot/P47804.html
- ↑ Mutations of the RGR gene; Retina International's scientific newsletter http://www.retina-international.com/sci-news/rgrmut.htm
- ↑ GeneReviews http://www.ncbi.nlm.nih.gov/sites/genetests/lab/gene/RGR