Calvarial Skull Defect Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C4025787
Similar Terms
Downloads & Tools

Genes

21 genes associated with the disease Calvarial Skull Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALX4 ALX homeobox 4
ARHGAP31 Rho GTPase activating protein 31
BMS1 BMS1 ribosome biogenesis factor
COL18A1 collagen, type XVIII, alpha 1
DLL4 delta-like 4 (Drosophila)
DOCK6 dedicator of cytokinesis 6
EOGT EGF domain-specific O-linked N-acetylglucosamine (GlcNAc) transferase
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1
HSPG2 heparan sulfate proteoglycan 2
LBR lamin B receptor
LETM1 leucine zipper-EF-hand containing transmembrane protein 1
MSX2 msh homeobox 2
NELFA negative elongation factor complex member A
NOTCH1 notch 1
NSD2 nuclear receptor binding SET domain protein 2
PCYT1A phosphate cytidylyltransferase 1, choline, alpha
RBPJ recombination signal binding protein for immunoglobulin kappa J region
UBR1 ubiquitin protein ligase E3 component n-recognin 1
WNT7A wingless-type MMTV integration site family, member 7A