Gene: NKX2-5 ×
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 		0.120 Biomarker phenotype BEFREE Heterozygous mutations in human protein coding genes NKX2-5 and RBM20 are associated with a wide array of pathological phenotypes some of which are sudden cardiac death, unexplained syncope and either combined or isolated congenital heart diseases such as dilated cardiomyopathy. 30611920 2020
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5 		0.120 GeneticVariation phenotype BEFREE A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype? 16896344 2006
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5 		0.120 Biomarker phenotype HPO