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Opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan)
Identifiers
Symbols OPN1MW; CBBM; CBD; GCP
External IDs OMIM303800 HomoloGene88332 GeneCards: OPN1MW Gene
Orthologs
Species Human Mouse
Entrez 2652 n/a
Ensembl n/a n/a
UniProt n/a n/a
RefSeq (mRNA) NM_000513 n/a
RefSeq (protein) NP_000504 n/a
Location (UCSC) n/a n/a
PubMed search [1] n/a

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

See also

References

Further reading

  • 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.  
  • 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.  
  • 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.  
  • 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. 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. 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.  
  • 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. doi:10.1038/383637a0. PMID 8857542.  
  • 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 ( Pt 3): 1201–8. 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.  
  • 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. 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.  
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