OPN5
| Opsin 5 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Identifikatori | |||||||||||
| Simboli | OPN5; GPR136; PGR12; TMEM13 | ||||||||||
| Vanjski ID | OMIM: 609042 MGI: 2662912 HomoloGene: 72341 IUPHAR: OPN5 GeneCards: OPN5 Gene | ||||||||||
| |||||||||||
| Ortolozi | |||||||||||
| Vrsta | Čovek | Miš | |||||||||
| Entrez | 221391 | 353344 | |||||||||
| Ensembl | ENSG00000124818 | ENSMUSG00000043972 | |||||||||
| UniProt | Q6U736 | Q059L5 | |||||||||
| RefSeq (mRNA) | NM_001030051 | NM_181753 | |||||||||
| RefSeq (protein) | NP_001025222 | NP_861418 | |||||||||
| Lokacija (UCSC) |
Chr 6: 47.86 - 47.9 Mb |
Chr 17: 42.02 - 42.07 Mb | |||||||||
| PubMed pretraga | [1] | [2] | |||||||||
OPN5, ili Opsin-5, je protein koji je kod čoveka kodiran OPN5 genom.[1][2][3]
Opsini su članovi familije G protein-spregnutih receptora. Ovaj opsinski gen je izražen u oku, mozgu, testisima, i kičmenoj moždini. On pripada sedam-eksonskog familiji sisarskih opsina koja obuhvata peropsin (RRH) i retinalni G protein spregnuti receptor (RGR). Kao i drugi opsinski geni, ovaj gen može da kodira protein sa fotoizomeraznom aktivnošću. Alternativno splajsovanje dovodi do višestrukih transkriptnih varijanti koje kodiraju različite izoforme.[3]
Vidi još
Literatura
- ^ Tarttelin EE, Bellingham J, Hankins MW, Foster RG, Lucas RJ (2003). „Neuropsin (Opn5): a novel opsin identified in mammalian neural tissue”. FEBS Lett. 554 (3): 410—6. PMID 14623103. doi:10.1016/S0014-5793(03)01212-2.
- ^ Fredriksson R, Hoglund PJ, Gloriam DE, Lagerstrom MC, Schioth HB (2003). „Seven evolutionarily conserved human rhodopsin G protein-coupled receptors lacking close relatives”. FEBS Lett. 554 (3): 381—8. PMID 14623098. doi:10.1016/S0014-5793(03)01196-7.
- ^ а б „Entrez Gene: OPN5 opsin 5”.
Dodatna literatura
- Terakita A (2006). „The opsins.”. Genome Biol.. 6 (3): 213. PMC 1088937
. PMID 15774036. doi:10.1186/gb-2005-6-3-213. - 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. PMC 139241
. PMID 12477932. doi:10.1073/pnas.242603899. - Vassilatis DK; Hohmann JG; Zeng H; et al. (2003). „The G protein-coupled receptor repertoires of human and mouse.”. Proc. Natl. Acad. Sci. U.S.A.. 100 (8): 4903—8. PMC 153653
. PMID 12679517. doi:10.1073/pnas.0230374100. - Mungall AJ; Palmer SA; Sims SK; et al. (2003). „The DNA sequence and analysis of human chromosome 6.”. Nature. 425 (6960): 805—11. PMID 14574404. doi:10.1038/nature02055.
- Ota T; Suzuki Y; Nishikawa T; et al. (2004). „Complete sequencing and characterization of 21,243 full-length human cDNAs.”. Nat. Genet.. 36 (1): 40—5. PMID 14702039. doi:10.1038/ng1285.
- 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. PMC 528928
. PMID 15489334. doi:10.1101/gr.2596504.
Content Disclaimer
Informasi ini disarikan dari Wikipedia dan disajikan kembali untuk tujuan edukasi. Konten tersedia di bawah lisensi CC BY-SA 3.0. Kami tidak bertanggung jawab atas ketidakakuratan data yang bersumber dari kontribusi publik tersebut.
- The information displayed on this website is sourced in part or in whole from Wikipedia and has been adapted for the purpose of restating it. We strive to provide accurate and relevant information, however:
- There is no guarantee of absolute accuracy. Wikipedia is an open, collaborative project that can be edited by anyone, so information is subject to change.
- It is not intended to constitute professional advice. The content displayed is for informational and educational purposes only. For important decisions (e.g., medical, legal, or financial), please consult a professional.
- Content copyright. Wikipedia is licensed under the Creative Commons Attribution-ShareAlike License (CC BY-SA). This means that content may be reused with appropriate attribution and shared under a similar license.
- Responsible use. Any risk arising from the use of information from this website is entirely the responsibility of the user.