red-sensitive opsin; red cone photoreceptor pigment (OPN1LW, RCP)
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Function
- component of visual pigment woth light absorption (max)=560 nm
- phosphorylated on some or all of the Ser & Thr present in the C-terminal region
Structure
- belongs to the G-protein coupled receptor 1 family opsin subfamily
Compartment
membrane
Expression
- the three color pigments are found in the cone photoreceptor cells
Pathology
- defects in OPN1LW are the cause of partial colorblindness protan series (protanopia)
More general terms
References
- ↑ UniProt http://www.uniprot.org/uniprot/P04000.html
- ↑ Mutations of the color pigment genes Retina International's Scientific Newsletter http://www.retina-international.com/sci-news/cppmut.htm
- ↑ GeneReviews https://www.genecards.org/cgi-bin/carddisp.pl?gene=OPN1LW