OPN1MW
Изглед
Opsin 1, senzitivan na srednje talasne dužine | |||||||||||
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Identifikatori | |||||||||||
Simboli | OPN1MW; CBBM; CBD; GCP | ||||||||||
Vanjski ID | OMIM: 303800 HomoloGene: 88332 GeneCards: OPN1MW Gene | ||||||||||
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Ortolozi | |||||||||||
Vrsta | Čovek | Miš | |||||||||
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 | |||||||||
Lokacija (UCSC) | n/a | n/a | |||||||||
PubMed pretraga | [1] | n/a |
OPN1MW, zeleno-senzitivni opsin, je protein koji je kod ljudi kodiran OPN1MW genom.[1]
Vidi još
[уреди | уреди извор]Literatura
[уреди | уреди извор]Dodatna literatura
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- 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. PMC 1219262
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- 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.