RecName: Full=Long-wave-sensitive opsin 1; AltName: Full=Red cone phot - Protein

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Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism. [Invest Ophthalmol Vis Sci. 2023]
Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism.
Wang Y, Sun W, Xiao X, Jiang Y, Ouyang J, Wang J, Yi Z, Li S, Jia X, Wang P, et al. Invest Ophthalmol Vis Sci. 2023 Apr 3; 64(4):29.
Insight from OPN1LW Gene Haplotypes into the Cause and Prevention of Myopia. [Genes (Basel). 2022]
Insight from OPN1LW Gene Haplotypes into the Cause and Prevention of Myopia.
Neitz M, Wagner-Schuman M, Rowlan JS, Kuchenbecker JA, Neitz J. Genes (Basel). 2022 May 25; 13(6). Epub 2022 May 25.
Visual and ocular findings in a family with X-linked cone dysfunction and protanopia. [Ophthalmic Genet. 2021]
Visual and ocular findings in a family with X-linked cone dysfunction and protanopia.
Holmquist D, Epstein D, Olsson M, Wissinger B, Kohl S, Hengstler J, Tear-Fahnehjelm K. Ophthalmic Genet. 2021 Oct; 42(5):570-576. Epub 2021 Jul 21.

RefSeq genomic sequence
See the genomic reference sequence for the OPN1LW gene (NG_009105.2).
RefSeq protein
See the reference protein sequence for long-wave-sensitive opsin 1 (NP_064445.2).

PubMed
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BioAssay by Target (Summary)
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Protein (RefSeq)
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P04000 [Domain Mapping of Disease Mut...]
P04000
Domain Mapping of Disease Mutations
Reactome [Reactome]
Reactome

RecName: Full=Long-wave-sensitive opsin 1; AltName: Full=Red cone photoreceptor ...
RecName: Full=Long-wave-sensitive opsin 1; AltName: Full=Red cone photoreceptor pigment; AltName: Full=Red-sensitive opsin; Short=ROP
gi|2203400462|sp|P04000.2|OPSR_HUMA

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