RRH
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| Retinal pigment epithelium-derived rhodopsin homolog | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||||||
| Symbols | RRH; | ||||||||||||
| External IDs | OMIM: 605224 MGI: 1097709 HomoloGene: 55977 GeneCards: RRH Gene | ||||||||||||
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| RNA expression pattern | |||||||||||||
| 250px | |||||||||||||
| More reference expression data | |||||||||||||
| Orthologs | |||||||||||||
| Species | Human | Mouse | |||||||||||
| Entrez | 10692 | 20132 | |||||||||||
| Ensembl | ENSG00000180245 | ENSMUSG00000028012 | |||||||||||
| UniProt | O14718 | Q543W9 | |||||||||||
| RefSeq (mRNA) | NM_006583 | NM_009102 | |||||||||||
| RefSeq (protein) | NP_006574 | NP_033128 | |||||||||||
| Location (UCSC) | Chr 4: 110.97 - 110.99 Mb | Chr 3: 129.8 - 129.81 Mb | |||||||||||
| PubMed search | [1] | [2] | |||||||||||
Visual pigment-like receptor peropsin is a protein that in humans is encoded by the RRH gene.[1][2]
Opsins are members of the guanine nucleotide-binding protein (G protein)-coupled receptor superfamily. This gene belongs to the seven-exon subfamily of mammalian opsin genes that includes opsin 5 and retinal G protein coupled receptor.[2]
References
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- Harrington JJ, Sherf B, Rundlett S; et al. (2001). "Creation of genome-wide protein expression libraries using random activation of gene expression". Nat. Biotechnol. 19 (5): 440–5. doi:10.1038/88107. PMID 11329013.
- Bellingham J, Wells DJ, Foster RG (2003). "In silico characterisation and chromosomal localisation of human RRH (peropsin)--implications for opsin evolution". BMC Genomics. 4 (1): 3. doi:10.1186/1471-2164-4-3. PMC 149353 Freely accessible. PMID 12542842.
- Barrios-Rodiles M, Brown KR, Ozdamar B; et al. (2005). "High-throughput mapping of a dynamic signaling network in mammalian cells". Science. 307 (5715): 1621–5. doi:10.1126/science.1105776. PMID 15761153.
- Rivolta C, Berson EL, Dryja TP (2007). "Mutation screening of the peropsin gene, a retinal pigment epithelium specific rhodopsin homolog, in patients with retinitis pigmentosa and allied diseases". Mol. Vis. 12: 1511–5. PMID 17167409.
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This article incorporates text from the United States National Library of Medicine, which is in the public domain.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ 2.0 2.1 "Entrez Gene: RRH retinal pigment epithelium-derived rhodopsin homolog".
