Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5 		0.700 Biomarker disease MGD Point mutations in murine Nkx2-5 phenocopy human congenital heart disease and induce pathogenic Wnt signaling. 28352650 2017
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5 		0.700 GermlineCausalMutation disease ORPHANET Familial atrial septal defect in the oval fossa with progressive prolongation of the atrioventricular conduction caused by mutations in the NKX2.5 gene. 19049681 2009
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5 		0.700 GermlineCausalMutation disease ORPHANET Clinical and genetic investigation of atrial septal defect with atrioventricular conduction defect in a large consanguineous Tunisian family. 18375255 2008
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5 		0.700 Biomarker disease GENOMICS_ENGLAND