Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 137814
Gene Symbol: NKX2-6
NKX2-6
CUI: C1857586
Disease: CONOTRUNCAL HEART MALFORMATIONS (disorder)
CONOTRUNCAL HEART MALFORMATIONS (disorder) 		0.700 GeneticVariation UNIPROT A novel NKX2.6 mutation associated with congenital ventricular septal defect. 25380965

2015
Entrez Id: 137814
Gene Symbol: NKX2-6
NKX2-6
CUI: C1857586
Disease: CONOTRUNCAL HEART MALFORMATIONS (disorder)
CONOTRUNCAL HEART MALFORMATIONS (disorder) 		0.700 GeneticVariation UNIPROT Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease. 25195019

2014
Entrez Id: 137814
Gene Symbol: NKX2-6
NKX2-6
CUI: C1857586
Disease: CONOTRUNCAL HEART MALFORMATIONS (disorder)
CONOTRUNCAL HEART MALFORMATIONS (disorder) 		0.700 GeneticVariation UNIPROT Conotruncal malformations and absent thymus due to a deleterious NKX2-6 mutation. 24421281

2014
Entrez Id: 137814
Gene Symbol: NKX2-6
NKX2-6
CUI: C1857586
Disease: CONOTRUNCAL HEART MALFORMATIONS (disorder)
CONOTRUNCAL HEART MALFORMATIONS (disorder) 		0.700 GeneticVariation UNIPROT Common arterial trunk associated with a homeodomain mutation of NKX2.6. 15649947

2005