InnateDB Protein
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IDBP-80811.7
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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RGR
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Protein Name
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retinal G protein coupled receptor
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Synonyms
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RP44;
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000350823
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InnateDB Gene
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IDBG-80807 (RGR)
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Protein Structure
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Function |
Receptor for all-trans- and 11-cis-retinal. Binds preferentially to the former and may catalyze the isomerization of the chromophore by a retinochrome-like mechanism.
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Subcellular Localization |
Membrane; Multi-pass membrane protein.
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Disease Associations |
Retinitis pigmentosa 44 (RP44) [MIM:613769]: A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. {ECO:0000269PubMed:10581022}. Note=The disease is caused by mutations affecting the gene represented in this entry.
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Tissue Specificity |
Preferentially expressed at high levels in the retinal pigment epithelium (RPE) and Mueller cells of the neural retina.
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
2
[view]
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Protein-Protein |
2
[view]
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Protein-DNA |
0
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR000276
G protein-coupled receptor, rhodopsin-like
IPR001793
Retinal pigment epithelium GPCR
IPR017452
GPCR, rhodopsin-like, 7TM
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PFAM |
PF00001
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PRINTS |
PR00237
PR00667
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PIRSF |
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SMART |
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TIGRFAMs |
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Modification |
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SwissProt |
P47804
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PhosphoSite |
PhosphoSite-
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TrEMBL |
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UniProt Splice Variant |
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Entrez Gene |
5995
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UniGene |
Hs.1544
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RefSeq |
NP_001012740
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HUGO |
HGNC:9990
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OMIM |
600342
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CCDS |
CCDS41543
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HPRD |
02642
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IMGT |
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EMBL |
AC022389
BC011349
BG912392
U14910
U14911
U15785
U15786
U15787
U15788
U15789
U15790
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GenPept |
AAA56748
AAB92384
AAH11349
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