Open Access Articles- Top Results for OPN1MW


External IDsOMIM300821 HomoloGene88332 GeneCards: OPN1MW Gene
RefSeq (mRNA)NM_000513n/a
RefSeq (protein)NP_000504n/a
Location (UCSC)Chr HG1497_PATCH:
153.35 – 153.36 Mb
PubMed search[1]n/a

Green-sensitive opsin is a protein that in humans is encoded by the OPN1MW gene.[1]

See also


External links

Further reading

  • Applebury ML, Hargrave PA (1987). "Molecular biology of the visual pigments.". Vision Res. 26 (12): 1881–95. PMID 3303660. doi:10.1016/0042-6989(86)90115-X. 
  • 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. PMID 1302020. doi:10.1038/ng0792-251. 
  • Neitz J, Neitz M, Jacobs GH (1990). "Analysis of fusion gene and encoded photopigment of colour-blind humans.". Nature 342 (6250): 679–82. PMID 2574415. doi:10.1038/342679a0. 
  • 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. doi:10.1126/science.2937147. 
  • Li ZY, Kljavin IJ, Milam AH (1995). "Rod photoreceptor neurite sprouting in retinitis pigmentosa.". J. Neurosci. 15 (8): 5429–38. PMID 7643192. 
  • Ladekjaer-Mikkelsen AS, Rosenberg T, Jørgensen AL (1996). "A new mechanism in blue cone monochromatism.". Hum. Genet. 98 (4): 403–8. PMID 8792812. doi:10.1007/s004390050229. 
  • 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. PMID 8857542. doi:10.1038/383637a0. 
  • 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. 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. PMID 10319869. doi:10.1038/8798. 
  • 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. PMID 12051694. doi:10.1016/S0006-291X(02)00458-8. 
  • 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. 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. PMID 16020309. doi:10.1080/13816810590968041. 

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