Congenital Pes Cavus Gene Set
Genes
19 genes associated with the disease Congenital Pes Cavus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ABHD12
|
abhydrolase domain containing 12
|
|
ALDH18A1
|
aldehyde dehydrogenase 18 family, member A1
|
|
ATP1A3
|
ATPase, Na+/K+ transporting, alpha 3 polypeptide
|
|
BIVM-ERCC5
|
BIVM-ERCC5 readthrough
|
|
CUL4B
|
cullin 4B
|
|
DNM2
|
dynamin 2
|
|
DYNC1H1
|
dynein, cytoplasmic 1, heavy chain 1
|
|
ERCC5
|
excision repair cross-complementation group 5
|
|
ERCC8
|
excision repair cross-complementation group 8
|
|
FBLN5
|
fibulin 5
|
|
FGD4
|
FYVE, RhoGEF and PH domain containing 4
|
|
FGFR1
|
fibroblast growth factor receptor 1
|
|
GJB1
|
gap junction protein, beta 1, 32kDa
|
|
MPZ
|
myelin protein zero
|
|
MTMR2
|
myotubularin related protein 2
|
|
NEFL
|
neurofilament, light polypeptide
|
|
PMP22
|
peripheral myelin protein 22
|
|
PTPRQ
|
protein tyrosine phosphatase, receptor type, Q
|
|
TWNK
|
twinkle mtDNA helicase
|
