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GENATLAS PHENOTYPE

last update : 5/09/2006

Symbol	RBP4
Location	10q23.33
Name	night blindness and progressive atrophy of the retinal pigment epithelium
Corresponding gene	RBP4
related resource	Retinal Information Network
Main clinical features	with retinol binding protein 4 deficiency
Genetic determination	autosomal recessive
Function/system disorder	eye
Type	disease

Gene product

Name	retinol binding protein 4, interstitial (RBP4)

Remark(s)