Congenital Lamellar 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/C0266537
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Genes

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

Symbol Name
BAP1 BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase)
BFSP1 beaded filament structural protein 1, filensin
BFSP2 beaded filament structural protein 2, phakinin
CRYAB crystallin, alpha B
CRYBA4 crystallin, beta A4
CRYGD crystallin, gamma D
CRYGS crystallin, gamma S
CYSLTR2 cysteinyl leukotriene receptor 2
GJA3 gap junction protein, alpha 3, 46kDa
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
GNAQ guanine nucleotide binding protein (G protein), q polypeptide
HSF4 heat shock transcription factor 4
IL2RG interleukin 2 receptor, gamma
MIP major intrinsic protein of lens fiber
PAX6 paired box 6
RECQL4 RecQ protein-like 4
SF3B1 splicing factor 3b, subunit 1, 155kDa
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1