Protein-coding gene in the species Homo sapiens
Blue-sensitive opsin is a protein that in humans is encoded by the OPN1SW gene .[5] [6] [7]
See also [ edit ] References [ edit ]
^ a b c GRCh38: Ensembl release 89: ENSG00000128617 - Ensembl , May 2017^ a b c GRCm38: Ensembl release 89: ENSMUSG00000058831 - Ensembl , May 2017^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .^ Nathans J, Thomas D, Hogness DS (Apr 1986). "Molecular genetics of human color vision: the genes encoding blue, green, and red pigments". Science . 232 (4747): 193–202. Bibcode :1986Sci...232..193N . CiteSeerX 10.1.1.461.5915 doi :10.1126/science.2937147 . PMID 2937147 . ^ Fitzgibbon J, Appukuttan B, Gayther S, Wells D, Delhanty J, Hunt DM (Feb 1994). "Localisation of the human blue cone pigment gene to chromosome band 7q31.3-32". Hum Genet . 93 (1): 79–80. doi :10.1007/bf00218919 . PMID 8270261 . S2CID 43548690 . ^ "Entrez Gene: OPN1SW opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)" .
Further reading [ edit ]
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 . S2CID 34038855 . 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 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 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. Bibcode :1989Sci...244..331S . 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. Bibcode :1986Sci...232..203N . 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. Bibcode :1997JMolE..44..378S . doi :10.1007/PL00006157 . PMID 9089077 . S2CID 6425474 . Scherer SW, Cheung J, MacDonald JR, et al. (2003). "Human Chromosome 7: DNA Sequence and Biology" . Science . 300 (5620): 767–72. Bibcode :2003Sci...300..767S . doi :10.1126/science.1083423 . PMC 2882961 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 . S2CID 3748083 .
