red-sensitive opsin; red cone photoreceptor pigment (OPN1LW, RCP)

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Function

Structure

Compartment

membrane

Expression

Pathology

  • defects in OPN1LW are the cause of partial colorblindness protan series (protanopia)

More general terms

References

  1. UniProt http://www.uniprot.org/uniprot/P04000.html
  2. Mutations of the color pigment genes Retina International's Scientific Newsletter http://www.retina-international.com/sci-news/cppmut.htm
  3. GeneReviews https://www.genecards.org/cgi-bin/carddisp.pl?gene=OPN1LW

Database