tetralogy of fallot Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [LS]. (Human Disease Ontology, DOID_6419)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:6419
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Genes

11 genes associated with the disease tetralogy of fallot in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
HECTD4 HECT domain containing E3 ubiquitin protein ligase 4 1.47454
GPC5 glypican 5 1.47287
NAA25 N(alpha)-acetyltransferase 25, NatB auxiliary subunit 1.40866
PTPN11 protein tyrosine phosphatase, non-receptor type 11 1.37501
ATXN2 ataxin 2 1.31332
SH2B3 SH2B adaptor protein 3 1.3016
NRP1 neuropilin 1 1.28906
RARRES1 retinoic acid receptor responder (tazarotene induced) 1 1.1572
FMN1 formin 1 0.92437
B4GALT1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 0.748112
ZNF532 zinc finger protein 532 0.668836