Protein-coding gene in the species Homo sapiens
OPN1MW Identifiers Aliases OPN1MW External IDs OMIM : 300821 HomoloGene : 88332 GeneCards : OPN1MW Wikidata
Green-sensitive opsin is a protein that in humans is encoded by the OPN1MW gene .[3] OPN1MW2 is a similar opsin.
See also [ edit ] References [ edit ] 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 . Winderickx J, Sanocki E, Lindsey DT, et al. (1993). "Defective colour vision associated with a missense mutation in the human green visual pigment gene". Nat. Genet . 1 (4): 251–6. doi :10.1038/ng0792-251 . PMID 1302020 . S2CID 23127406 . Neitz J, Neitz M, Jacobs GH (1990). "Analysis of fusion gene and encoded photopigment of colour-blind humans". Nature . 342 (6250): 679–82. doi :10.1038/342679a0 . PMID 2574415 . S2CID 4273929 . 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. Bibcode :1986Sci...232..193N . CiteSeerX 10.1.1.461.5915 doi :10.1126/science.2937147 . PMID 2937147 . Li ZY, Kljavin IJ, Milam AH (1995). "Rod photoreceptor neurite sprouting in retinitis pigmentosa" . J. Neurosci . 15 (8): 5429–38. doi :10.1523/JNEUROSCI.15-08-05429.1995 . PMC 6577619 PMID 7643192 . Ladekjaer-Mikkelsen AS, Rosenberg T, Jørgensen AL (1996). "A new mechanism in blue cone monochromatism". Hum. Genet . 98 (4): 403–8. doi :10.1007/s004390050229 . PMID 8792812 . S2CID 11799731 . Ferreira PA, Nakayama TA, Pak WL, Travis GH (1996). "Cyclophilin-related protein RanBP2 acts as chaperone for red/green opsin". Nature . 383 (6601): 637–40. Bibcode :1996Natur.383..637F . doi :10.1038/383637a0 . PMID 8857542 . S2CID 4304490 . Vissers PM, Bovee-Geurts PH, Portier MD, et al. (1998). "Large-scale production and purification of the human green cone pigment: characterization of late photo-intermediates" . Biochem. J . 330 (3): 1201–8. doi :10.1042/bj3301201 . PMC 1219262 PMID 9494086 . Bernstein SL, Wong P (1998). "Regional expression of disease-related genes in human and monkey retina". Mol. Vis . 4 : 24. PMID 9815288 . Hayashi T, Motulsky AG, Deeb SS (1999). "Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype". Nat. Genet . 22 (1): 90–3. doi :10.1038/8798 . PMID 10319869 . S2CID 1326234 . Ueyama H, Kuwayama S, Imai H, et al. (2002). "Novel missense mutations in red/green opsin genes in congenital color-vision deficiencies". Biochem. Biophys. Res. Commun . 294 (2): 205–9. doi :10.1016/S0006-291X(02)00458-8 . PMID 12051694 . Zhu X, Brown B, Li A, et al. (2003). "GRK1-dependent phosphorylation of S and M opsins and their binding to cone arrestin during cone phototransduction in the mouse retina" . J. Neurosci . 23 (14): 6152–60. doi :10.1523/JNEUROSCI.23-14-06152.2003 . PMC 6740345 PMID 12853434 . Bonilha VL, Hollyfield JG, Grover S, Fishman GA (2005). "Abnormal distribution of red/green cone opsins in a patient with an autosomal dominant cone dystrophy". Ophthalmic Genet . 26 (2): 69–76. doi :10.1080/13816810590968041 . PMID 16020309 . S2CID 24486298 .
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