Heart Septal Defects Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

15 genes associated with the Heart Septal Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABCG2 ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group)
CBS cystathionine-beta-synthase
CFC1 cripto, FRL-1, cryptic family 1
CRELD1 cysteine-rich with EGF-like domains 1
FOXP1 forkhead box P1
GATA4 GATA binding protein 4
HAND1 heart and neural crest derivatives expressed 1
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
NKX2-5 NK2 homeobox 5
ROCK2 Rho-associated, coiled-coil containing protein kinase 2
SLC19A1 solute carrier family 19 (folate transporter), member 1
TYMS thymidylate synthetase
VEGFA vascular endothelial growth factor A