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GENATLAS PHENOTYPE

last update : 23-12-2014

Symbol	CBP
Location	Xq28
Name	color blindness, protan series, partial
Other name(s)	protanopia red colorblindness
Corresponding gene	OPN1LW
related resource	Retinal Information Network
Main clinical features	red-green color vision-defect protan color-vision defects appeared always associated with 5-prime red-green hybrid genes
Genetic determination	sex linked
Function/system disorder	eye
Type	disease

Gene product

Name	cone pigment, red (OPN1LW), opsin1

Remark(s)