UNC119

unc-119 lipid binding chaperone
OMIM: 604011
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Achromatopsia, Cone, and Cone-rod Dystrophy, Eye Disorders, Cone-Rod Dystrophy, Dominant, CD4 lymphopenia, idiopathic (Gorska (2012) Blood 119, 1399)