Congenital Absence Of Hand Gene Set
Genes
18 genes associated with the disease Congenital Absence Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ARHGAP31
|
Rho GTPase activating protein 31
|
|
BTRC
|
beta-transducin repeat containing E3 ubiquitin protein ligase
|
|
DLL4
|
delta-like 4 (Drosophila)
|
|
DLX5
|
distal-less homeobox 5
|
|
DLX6
|
distal-less homeobox 6
|
|
DOCK6
|
dedicator of cytokinesis 6
|
|
EOGT
|
EGF domain-specific O-linked N-acetylglucosamine (GlcNAc) transferase
|
|
EPS15L1
|
epidermal growth factor receptor pathway substrate 15-like 1
|
|
IKBKG
|
inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
|
|
LMBR1
|
limb development membrane protein 1
|
|
NOTCH1
|
notch 1
|
|
PLXND1
|
plexin D1
|
|
RBPJ
|
recombination signal binding protein for immunoglobulin kappa J region
|
|
REV3L
|
REV3-like, polymerase (DNA directed), zeta, catalytic subunit
|
|
SHFM1
|
split hand/foot malformation (ectrodactyly) type 1
|
|
TBX3
|
T-box 3
|
|
TP63
|
tumor protein p63
|
|
WNT10B
|
wingless-type MMTV integration site family, member 10B
|
