cataract Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A lens disease characterized by clouding of the lens inside the eye which leads to a decrease in vision. (Human Disease Ontology, DOID_83)
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10 genes associated with the disease cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CRYGA crystallin, gamma A
CRYGB crystallin, gamma B
DMPK dystrophia myotonica-protein kinase
ERCC2 excision repair cross-complementation group 2
GJA8 gap junction protein, alpha 8, 50kDa
GSTM1 glutathione S-transferase mu 1
GSTT1 glutathione S-transferase theta 1
NAT2 N-acetyltransferase 2 (arylamine N-acetyltransferase)
SLC16A12 solute carrier family 16, member 12
XRCC1 X-ray repair complementing defective repair in Chinese hamster cells 1