OPN1SW
From Self-sufficiency
| edit |
| Opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan) | |||||||||||||
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| Identifiers | |||||||||||||
| Symbols | OPN1SW; BCP; BOP; CBT | ||||||||||||
| External IDs | OMIM: 190900 MGI: 99438 HomoloGene: 1291 GeneCards: OPN1SW Gene | ||||||||||||
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| RNA expression pattern | |||||||||||||
| 250px | |||||||||||||
| More reference expression data | |||||||||||||
| Orthologs | |||||||||||||
| Species | Human | Mouse | |||||||||||
| Entrez | 611 | 12057 | |||||||||||
| Ensembl | ENSG00000128617 | ENSMUSG00000058831 | |||||||||||
| UniProt | P03999 | P51491 | |||||||||||
| RefSeq (mRNA) | NM_001708 | NM_007538 | |||||||||||
| RefSeq (protein) | NP_001699 | NP_031564 | |||||||||||
| Location (UCSC) | Chr 7: 128.2 - 128.2 Mb | Chr 6: 29.33 - 29.33 Mb | |||||||||||
| PubMed search | [1] | [2] | |||||||||||
Blue-sensitive opsin is a protein that in humans is encoded by the OPN1SW gene.[1][2][3]
See also
References
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- Applebury ML, Hargrave PA (1987). "Molecular biology of the visual pigments". Vision Res. 26 (12): 1881–95. doi:10.1016/0042-6989(86)90115-X. PMID 3303660.
- Swanson WH, Cohen JM (2003). "Color vision". Ophthalmology clinics of North America. 16 (2): 179–203. doi:10.1016/S0896-1549(03)00004-X. PMID 12809157.
- Weitz CJ, Went LN, Nathans J (1992). "Human tritanopia associated with a third amino acid substitution in the blue-sensitive visual pigment". Am. J. Hum. Genet. 51 (2): 444–6. PMC 1682686 Freely accessible. PMID 1386496.
- Weitz CJ, Miyake Y, Shinzato K; et al. (1992). "Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin". Am. J. Hum. Genet. 50 (3): 498–507. PMC 1684278 Freely accessible. PMID 1531728.
- Oprian DD, Asenjo AB, Lee N, Pelletier SL (1992). "Design, chemical synthesis, and expression of genes for the three human color vision pigments". Biochemistry. 30 (48): 11367–72. doi:10.1021/bi00112a002. PMID 1742276.
- Sarkar G, Sommer SS (1989). "Access to a messenger RNA sequence or its protein product is not limited by tissue or species specificity". Science. 244 (4902): 331–4. doi:10.1126/science.2565599. PMID 2565599.
- Nathans J, Piantanida TP, Eddy RL; et al. (1986). "Molecular genetics of inherited variation in human color vision". Science. 232 (4747): 203–10. doi:10.1126/science.3485310. PMID 3485310.
- Shimmin LC, Mai P, Li WH (1997). "Sequences and evolution of human and squirrel monkey blue opsin genes". J. Mol. Evol. 44 (4): 378–82. doi:10.1007/PL00006157. PMID 9089077.
- Scherer SW, Cheung J, MacDonald JR; et al. (2003). "Human chromosome 7: DNA sequence and biology". Science. 300 (5620): 767–72. doi:10.1126/science.1083423. PMC 2882961 Freely accessible. PMID 12690205.
- Gunther KL, Neitz J, Neitz M (2006). "A novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defect". Vis. Neurosci. 23 (3-4): 403–9. doi:10.1017/S0952523806233169. PMID 16961973.
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- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ "Entrez Gene: OPN1SW opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)".
