Subcapsular Cataract Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A cataract that affects the region of the lens directly beneath the capsule of the lens. (Human Phenotype Ontology, HP_0000523)
External Link https://www.disgenet.org/browser/0/1/0/C0235259
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Genes

17 genes associated with the disease Subcapsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABHD12 abhydrolase domain containing 12
ABHD5 abhydrolase domain containing 5
ACTB actin, beta
ALDH18A1 aldehyde dehydrogenase 18 family, member A1
ALMS1 Alstrom syndrome protein 1
ARL3 ADP-ribosylation factor-like 3
CCN2 cellular communication network factor 2
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
FOXC1 forkhead box C1
FOXE3 forkhead box E3
FZD4 frizzled class receptor 4
LRP5 low density lipoprotein receptor-related protein 5
OAT ornithine aminotransferase
PAX6 paired box 6
PITX2 paired-like homeodomain 2
TGFB1 transforming growth factor, beta 1
UNC45B unc-45 homolog B (C. elegans)