Irido-Corneal Dysgenesis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0266525
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Genes

22 genes associated with the disease Irido-Corneal Dysgenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARSD arylsulfatase D
BFSP2 beaded filament structural protein 2, phakinin
BMP4 bone morphogenetic protein 4
COL4A1 collagen, type IV, alpha 1
CPAMD8 C3 and PZP-like, alpha-2-macroglobulin domain containing 8
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
FGFR2 fibroblast growth factor receptor 2
FOXC1 forkhead box C1
FOXD3 forkhead box D3
FOXE3 forkhead box E3
MAF v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
MSX2 msh homeobox 2
NR2E1 nuclear receptor subfamily 2, group E, member 1
PAX6 paired box 6
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit beta
PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta
PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
PITX2 paired-like homeodomain 2
PITX3 paired-like homeodomain 3
PXDN peroxidasin
SMO smoothened, frizzled class receptor