GATA4, GATA binding protein 4, 2626

N. diseases: 336; N. variants: 72
Disease: VENTRICULAR SEPTAL DEFECT 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3280777
Disease: VENTRICULAR SEPTAL DEFECT 1
VENTRICULAR SEPTAL DEFECT 1 		0.600 GeneticVariation disease UNIPROT A novel GATA4 loss-of-function mutation associated with congenital ventricular septal defect. 22101736 2012
CUI: C3280777
Disease: VENTRICULAR SEPTAL DEFECT 1
VENTRICULAR SEPTAL DEFECT 1 		0.600 GeneticVariation disease UNIPROT A novel GATA4 mutation responsible for congenital ventricular septal defects. 21637914 2011
CUI: C3280777
Disease: VENTRICULAR SEPTAL DEFECT 1
VENTRICULAR SEPTAL DEFECT 1 		0.600 GeneticVariation disease UNIPROT Mutations of the GATA4 and NKX2.5 genes in Chinese pediatric patients with non-familial congenital heart disease. 21110066 2010
CUI: C3280777
Disease: VENTRICULAR SEPTAL DEFECT 1
VENTRICULAR SEPTAL DEFECT 1 		0.600 GeneticVariation disease UNIPROT GATA4 mutations in 486 Chinese patients with congenital heart disease. 18672102 2009
CUI: C3280777
Disease: VENTRICULAR SEPTAL DEFECT 1
VENTRICULAR SEPTAL DEFECT 1 		0.600 CausalMutation disease CLINVAR
CUI: C3280777
Disease: VENTRICULAR SEPTAL DEFECT 1
VENTRICULAR SEPTAL DEFECT 1 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C3280777
Disease: VENTRICULAR SEPTAL DEFECT 1
VENTRICULAR SEPTAL DEFECT 1 		0.600 Biomarker disease GENOMICS_ENGLAND