OPN3
Opsin 3 | |||||||||||||
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Identifiers | |||||||||||||
Symbols | OPN3 ; ECPN; PPP1R116 | ||||||||||||
External IDs | OMIM: 606695 MGI: 1338022 HomoloGene: 40707 IUPHAR: 160 GeneCards: OPN3 Gene | ||||||||||||
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RNA expression pattern | |||||||||||||
More reference expression data | |||||||||||||
Orthologs | |||||||||||||
Species | Human | Mouse | |||||||||||
Entrez | 23596 | 13603 | |||||||||||
Ensembl | ENSG00000054277 | ENSMUSG00000026525 | |||||||||||
UniProt | Q9H1Y3 | Q9WUK7 | |||||||||||
RefSeq (mRNA) | NM_001030011 | NM_010098 | |||||||||||
RefSeq (protein) | NP_055137 | NP_034228 | |||||||||||
Location (UCSC) | Chr 1: 241.75 – 241.84 Mb | Chr 1: 175.66 – 175.69 Mb | |||||||||||
PubMed search | |||||||||||||
Opsin-3 is a protein that, in humans, is encoded by the OPN3 gene.[1][2][3] Alternative splicing of this gene results in multiple transcript variants encoding different protein isoforms.
Function
Opsins are members of the G protein-coupled receptor superfamily. In addition to the visual opsins, mammals possess several photoreceptive non-visual opsins that are expressed in tissues outside the eye. The opsin-3 gene is strongly expressed in brain and testis and weakly expressed in liver, placenta, heart, lung, skeletal muscle, kidney, and pancreas. The gene may also be expressed in the retina. The protein has the canonical features of a photoreceptive opsin protein.[3]
References
- ↑ Blackshaw S, Snyder SH (Jun 1999). "Encephalopsin: a novel mammalian extraretinal opsin discretely localized in the brain". J Neurosci 19 (10): 3681–90. PMID 10234000.
- ↑ Halford S, Freedman MS, Bellingham J, Inglis SL, Poopalasundaram S, Soni BG, Foster RG, Hunt DM; Freedman (Jun 2001). "Characterization of a novel human opsin gene with wide tissue expression and identification of embedded and flanking genes on chromosome 1q43". Genomics 72 (2): 203–8. doi:10.1006/geno.2001.6469. PMID 11401433.
- ↑ 3.0 3.1 "Entrez Gene: OPN3 opsin 3 (encephalopsin, panopsin)".
Further reading
- Bonaldo MF; Lennon G; Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
- Halford S; Bellingham J; Ocaka L et al. (2002). "Assignment of panopsin (OPN3) to human chromosome band 1q43 by in situ hybridization and somatic cell hybrids". Cytogenet. Cell Genet. 95 (3–4): 234–5. doi:10.1159/000059351. PMID 12063405.
- Kasper G; Taudien S; Staub E et al. (2003). "Different structural organization of the encephalopsin gene in man and mouse". Gene 295 (1): 27–32. doi:10.1016/S0378-1119(02)00799-0. PMID 12242008.
- Strausberg RL; Feingold EA; Grouse LH et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Alam NA; Gorman P; Jaeger EE et al. (2004). "Germline deletions of EXO1 do not cause colorectal tumors and lesions which are null for EXO1 do not have microsatellite instability". Cancer Genet. Cytogenet. 147 (2): 121–7. doi:10.1016/S0165-4608(03)00196-1. PMID 14623461.
- Gerhard DS; Wagner L; Feingold EA et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Gregory SG; Barlow KF; McLay KE et al. (2006). "The DNA sequence and biological annotation of human chromosome 1". Nature 441 (7091): 315–21. doi:10.1038/nature04727. PMID 16710414.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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