Congenital Total Cataract Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0266539
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
AGK acylglycerol kinase
CRYAA crystallin, alpha A
CRYBB2 crystallin, beta B2
CRYGB crystallin, gamma B
DNMBP dynamin binding protein
EPHA2 EPH receptor A2
FYCO1 FYVE and coiled-coil domain containing 1
GCNT2 glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group)
GJA8 gap junction protein, alpha 8, 50kDa
HSF4 heat shock transcription factor 4
LEMD2 LEM domain containing 2
LIM2 lens intrinsic membrane protein 2, 19kDa
LSS lanosterol synthase (2,3-oxidosqualene-lanosterol cyclase)
MIP major intrinsic protein of lens fiber
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)
SIPA1L3 signal-induced proliferation-associated 1 like 3