OPN1SW edit Opsin 1 (pigment kupe) Identifikatori Simboli OPN1SW; BCP; BOP; CBT Vanjski ID OMIM: 190900 MGI: 99438 HomoloGene: 1291 GeneCards: OPN1SW Gene Ontologija gena Molekularna funkcija • aktivnost rodopsinu-sličnog receptora • receptorska aktivnost • aktivnost fotorecptora plave svetlosti Celularna komponenta • fotoreceptorski spoljašnje segment • integralno sa ćelijskom membranom • membrana Biološki proces • prenos signala • signalni put G-protein spregnutog receptora • vizuelna percepcija • fototransdukcija • protein-hromofor veza • respons na stimulus Pregled RNK izražavanja podaci Ortolozi Vrsta Čovek Miš Entrez 611 12057 Ensembl ENSG00000128617 ENSMUSG00000058831 UniProt P03999 P51491 RefSeq (mRNA) NM_001708 NM_007538 RefSeq (protein) NP_001699 NP_031564 Lokacija (UCSC) Chr 7: 128.2 - 128.2 Mb Chr 6: 29.33 - 29.33 Mb PubMed pretraga [1] [2] OPN1SW, plavo-senzitivni opsin je protein koji je kod ljudi kodiran OPN1SW genom.[1][2][3] Povezano Opsin Literatura ↑ 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. 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. PMID 8270261.  ↑ „Entrez Gene: OPN1SW opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)”.  Dodatna literatura 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.  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. 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. 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. DOI:10.1007/PL00006157. PMID 9089077.  Scherer SW, Cheung J, MacDonald JR, et al. (2003). „Human chromosome 7: DNA sequence and biology.”. Science 300 (5620): 767–72. 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.

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