OPN1MW2
id:
opn1mw2-299-915773
title:
OPN1MW2
text:
OPN1MW2 is a duplication of the OPN1MW gene, which encodes the medium wavelength sensitive (MWS) photopsin. The gene duplication is present in about 50% of X-chromosomes, so is present in 50% of males and at least once 75% of females. It caused by the same mechanism that causes congenital red-green color blindness, the most common form of color blindness.
brand slug:
wiki
category slug:
encyclopedia
description:
Human protein
original url:
https://en.wikipedia.org/wiki/OPN1MW2
date created:
date modified:
2023-12-30T10:01:16Z
main entity:
{"identifier":"Q23301892","url":"https://www.wikidata.org/entity/Q23301892"}
image:
fields total:
13
integrity:
14