conotruncal defect Gene Set

Dataset	GWASdb SNP-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	A congenital malformation of the outflow tract of the heart. Conotruncal defects are thought to result from a disturbance of the outflow tract of the embryonic heart, and comprise truncus arteriosus, tetralogy of Fallot, interrupted aortic arch, transposition of the great arteries, and double outlet right ventricle. (Human Phenotype Ontology, HP_0001710)
External Link	http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0001710
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Genes

11 genes associated with the conotruncal defect phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol	Name	Standardized Value
HECTD4	HECT domain containing E3 ubiquitin protein ligase 4	1.31017
GPC5	glypican 5	1.30781
NAA25	N(alpha)-acetyltransferase 25, NatB auxiliary subunit	1.23237
PTPN11	protein tyrosine phosphatase, non-receptor type 11	1.20113
ATXN2	ataxin 2	1.15067
SH2B3	SH2B adaptor protein 3	1.1396
NRP1	neuropilin 1	1.12851
RARRES1	retinoic acid receptor responder (tazarotene induced) 1	1.01065
FMN1	formin 1	0.813733
B4GALT1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	0.647116
ZNF532	zinc finger protein 532	0.572823