Abnormality Of The Abdominal Wall Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description The presence of any abnormality affecting the abdominal wall. (Human Phenotype Ontology, HP_0004298)
External Link https://www.disgenet.org/browser/0/1/0/C4021664
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Genes

17 genes associated with the disease Abnormality Of The Abdominal Wall in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APC adenomatous polyposis coli
B3GAT3 beta-1,3-glucuronyltransferase 3
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
COL2A1 collagen, type II, alpha 1
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
DDRGK1 DDRGK domain containing 1
FAH fumarylacetoacetate hydrolase (fumarylacetoacetase)
FUCA1 fucosidase, alpha-L- 1, tissue
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HSPG2 heparan sulfate proteoglycan 2
IFT122 intraflagellar transport 122
INSR insulin receptor
PITX2 paired-like homeodomain 2
SUZ12 SUZ12 polycomb repressive complex 2 subunit
USP9X ubiquitin specific peptidase 9, X-linked