Congenital Foot Deformity Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0016508
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Genes

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

Symbol Name
AFF3 AF4/FMR2 family, member 3
CKAP4 cytoskeleton-associated protein 4
DLX5 distal-less homeobox 5
DLX6 distal-less homeobox 6
DYNC1I1 dynein, cytoplasmic 1, intermediate chain 1
EPS15L1 epidermal growth factor receptor pathway substrate 15-like 1
FGD1 FYVE, RhoGEF and PH domain containing 1
GLI2 GLI family zinc finger 2
HOXD13 homeobox D13
LMNA lamin A/C
OCM oncomodulin
PTHLH parathyroid hormone-like hormone
RPE65 retinal pigment epithelium-specific protein 65kDa
SALL4 spalt-like transcription factor 4
SHFM1 split hand/foot malformation (ectrodactyly) type 1
TP63 tumor protein p63
UVRAG UV radiation resistance associated