OPN1SW
From Wikipedia, the free encyclopedia
Opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)
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Identifiers | ||||||||||||||
Symbol(s) | OPN1SW; BCP; BOP; CBT | |||||||||||||
External IDs | OMIM: 190900 MGI: 99438 HomoloGene: 1291 | |||||||||||||
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RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 611 | 12057 | ||||||||||||
Ensembl | ENSG00000128617 | ENSMUSG00000058831 | ||||||||||||
Uniprot | P03999 | P51491 | ||||||||||||
Refseq | NM_001708 (mRNA) NP_001699 (protein) |
NM_007538 (mRNA) NP_031564 (protein) |
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Location | Chr 7: 128.2 - 128.2 Mb | Chr 6: 29.33 - 29.33 Mb | ||||||||||||
Pubmed search | [1] | [2] |
Opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan), also known as OPN1SW, is a human gene.[1]
[edit] See also
[edit] References
[edit] Further reading
- Applebury ML, Hargrave PA (1987). "Molecular biology of the visual pigments.". Vision Res. 26 (12): 1881-95. PMID 3303660.
- Swanson WH, Cohen JM (2003). "Color vision.". Ophthalmology clinics of North America 16 (2): 179-203. 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. 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. 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. 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. PMID 2565599.
- Nathans J, Thomas D, Hogness DS (1986). "Molecular genetics of human color vision: the genes encoding blue, green, and red pigments.". Science 232 (4747): 193-202. PMID 2937147.
- Nathans J, Piantanida TP, Eddy RL, et al. (1986). "Molecular genetics of inherited variation in human color vision.". Science 232 (4747): 203-10. PMID 3485310.
- Fitzgibbon J, Appukuttan B, Gayther S, et al. (1994). "Localisation of the human blue cone pigment gene to chromosome band 7q31.3-32.". Hum. Genet. 93 (1): 79-80. PMID 8270261.
- 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. PMID 9089077.
- Scherer SW, Cheung J, MacDonald JR, et al. (2003). "Human chromosome 7: DNA sequence and biology.". Science 300 (5620): 767-72. doi: . 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: . PMID 16961973.