congenital heart disease Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_1682)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:1682
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Genes

25 genes associated with the disease congenital heart disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
MAML3 mastermind-like 3 (Drosophila) 1.65612
SLC9A3R2 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 2 1.34276
HLA-B major histocompatibility complex, class I, B 1.15841
PIEZO1 piezo-type mechanosensitive ion channel component 1 1.09864
SLC17A3 solute carrier family 17 (organic anion transporter), member 3 1.07539
ZNF385D zinc finger protein 385D 1.04692
REXO4 REX4, RNA exonuclease 4 homolog (S. cerevisiae) 0.905653
HECTD4 HECT domain containing E3 ubiquitin protein ligase 4 0.754533
GPC5 glypican 5 0.75119
NAA25 N(alpha)-acetyltransferase 25, NatB auxiliary subunit 0.650844
PTPN11 protein tyrosine phosphatase, non-receptor type 11 0.625588
MYLK myosin light chain kinase 0.620165
ZBTB16 zinc finger and BTB domain containing 16 0.601018
ATXN2 ataxin 2 0.579661
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A 0.574603
AXIN1 axin 1 0.56878
SH2B3 SH2B adaptor protein 3 0.567655
NRP1 neuropilin 1 0.555938
PDIA2 protein disulfide isomerase family A, member 2 0.553041
CD44 CD44 molecule (Indian blood group) 0.497937
CSF1R colony stimulating factor 1 receptor 0.49686
RARRES1 retinoic acid receptor responder (tazarotene induced) 1 0.486328
FMN1 formin 1 0.466906
B4GALT1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 0.448729
ZNF532 zinc finger protein 532 0.438494