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OPN1SW

Official Full Name
opsin 1, short wave sensitive
Organism
Homo sapiens
GeneID
611
Background
This gene belongs to the G-protein coupled receptor 1 family, opsin subfamily. It encodes the blue cone pigment gene which is one of three types of cone photoreceptors responsible for normal color vision. Defects in this gene are the cause of tritan color blindness (tritanopia). Affected individuals lack blue and yellow sensory mechanisms while retaining those for red and green. Defective blue vision is characteristic. [provided by RefSeq, Jul 2008]
Synonyms
BCP; BOP; CBT;

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