blindness; optic atrophy, hereditary, leber Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group vision (Genetic Association Database)
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Genes

8 genes associated with the disease blindness; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
AIPL1 aryl hydrocarbon receptor interacting protein-like 1
CEP290 centrosomal protein 290kDa
CRB1 crumbs family member 1, photoreceptor morphogenesis associated
CRX cone-rod homeobox
GUCY2D guanylate cyclase 2D, membrane (retina-specific)
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
RDH12 retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
RPE65 retinal pigment epithelium-specific protein 65kDa