congenital heart defects; heart defects, congenital Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group developmental (Genetic Association Database)
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Genes

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

Symbol Name
APOE apolipoprotein E
ARHGDIG Rho GDP dissociation inhibitor (GDI) gamma
AXIN1 axin 1
BAG6 BCL2-associated athanogene 6
BHMT betaine--homocysteine S-methyltransferase
CBS cystathionine-beta-synthase
CCL2 chemokine (C-C motif) ligand 2
CD44 CD44 molecule (Indian blood group)
CITED2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
CSF1R colony stimulating factor 1 receptor
DHFR dihydrofolate reductase
ENG endoglin
FBLN1 fibulin 1
GATA4 GATA binding protein 4
GATA6 GATA binding protein 6
HAND2 heart and neural crest derivatives expressed 2
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
ISL1 ISL LIM homeobox 1
LEF1 lymphoid enhancer-binding factor 1
MTHFD1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
MYLK myosin light chain kinase
NKX2-5 NK2 homeobox 5
PDIA2 protein disulfide isomerase family A, member 2
PRRC2A proline-rich coiled-coil 2A
REXO4 REX4, RNA exonuclease 4 homolog (S. cerevisiae)
SCNN1A sodium channel, non voltage gated 1 alpha subunit
SHMT1 serine hydroxymethyltransferase 1 (soluble)
TCN2 transcobalamin II
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A
ZBTB16 zinc finger and BTB domain containing 16