heart anomalies, congenital Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group cardiovascular (Genetic Association Database)
Similar Terms
Downloads & Tools

Genes

16 genes associated with the disease heart anomalies, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ADD1 adducin 1 (alpha)
CITED2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
CKM creatine kinase, muscle
F2 coagulation factor II (thrombin)
F7 coagulation factor VII (serum prothrombin conversion accelerator)
GJA1 gap junction protein, alpha 1, 43kDa
HOXC4 homeobox C4
HOXC5 homeobox C5
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
MS multiple sclerosis
MTHFD1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NOS3 nitric oxide synthase 3 (endothelial cell)
NPPA natriuretic peptide A
SLC19A1 solute carrier family 19 (folate transporter), member 1
TNF tumor necrosis factor