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| Opsin 1 (cone pigments), long-wave-sensitive (color blindness, protan) | |||||||||||||
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| Identifiers | |||||||||||||
| Symbols | OPN1LW; CBP; CBBM; RCP | ||||||||||||
| External IDs | OMIM: 303900 MGI: 1097692 HomoloGene: 68064 GeneCards: OPN1LW Gene | ||||||||||||
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| RNA expression pattern | |||||||||||||
| More reference expression data | |||||||||||||
| Orthologs | |||||||||||||
| Species | Human | Mouse | |||||||||||
| Entrez | 5956 | 14539 | |||||||||||
| Ensembl | ENSG00000102076 | ENSMUSG00000031394 | |||||||||||
| UniProt | P04000 | O35599 | |||||||||||
| RefSeq (mRNA) | NM_020061 | NM_008106 | |||||||||||
| RefSeq (protein) | NP_064445 | NP_032132 | |||||||||||
| Location (UCSC) | Chr X: 153.06 - 153.08 Mb |
Chr X: 70.38 - 70.4 Mb |
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| PubMed search | [1] | [2] | |||||||||||
Red-sensitive opsin is a protein that in humans is encoded by the OPN1LW gene.[1]
This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called red cone photopigment or long-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. This gene and the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of partial, protanopic colorblindness.[1]
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This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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