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OPN1LW
| Symbol: | OPN1LW | | Name(s): | opsin 1 (cone pigments), long-wave-sensitive (color blindness, protan) | | Type: | protein-coding | | Organism: | Homo sapiens | | Synonyms: | CBBM, CBP, RCP | | Links: |
Pubmed,
Entrez Gene,
GeneCards,
BioGPS,
Map Viewer.
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Gene Information from Publications |
| Publication Link |
Summary of findings |
| 12051694 |
In a Japanese male with congenital protan red/green color blindness the mutation Gly338Glu (GGG-->GAG) occurred in the single red gene resulting in no absorbance and loss of function |
| 16020309 |
Abnormal distribution of cone red opsin is associated with autosomal dominant cone dystrophy |
Recent Publications on OPN1LW: |  |
Different selective pressures shape the molecular evolution of color vision in chimpanzee and human populations.
A population genetic analysis of the long-wavelength opsin (OPN1LW, "red")... | 17th December, 2008
| Center for Evolutionary Functional Genomics, The Biodesign Institute and
| Mol Biol Evol. 2008 Dec;25(12):2735-43. Epub 2008 Oct 1.
DOI Direct Link |
Identification of novel retinal target genes of thyroid hormone in the human WERI cells by expression microarray analysis.
Using the human WERI-Rb1 cell line as a model system, we performed a... | 25th October, 2007
| Division of Medical Genetics, Departments of Medicine and Genome Sciences,
| Vision Res. 2007 Aug;47(17):2314-26. Epub 2007 Jul 25.
DOI Direct Link |
Signatures of selection and gene conversion associated with human color vision variation.
Trichromatic color vision in humans results from the combination of red,... | 21st September, 2004
| Department of Biology, University of Maryland, College Park 20742, USA.
| Am J Hum Genet. 2004 Sep;75(3):363-75. Epub 2004 Jul 13.
DOI Direct Link |
OPN1LW results (if any) from reagent suppliers | 
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