Cytoscape Web
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NKX2-5
10 associated diseases
6 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Athyreosis
Atrial septal defect - atrioventricular conduction defects
Atrial septal defect, ostium secundum type
Familial atrial fibrillation
Familial isolated congenital asplenia
Familial progressive cardiac conduction defect
Hypoplastic left heart syndrome
Single ventricular septal defect
Tetralogy of Fallot
Thyroid hypoplasia
Gene symbol Score
(click on to see the evidence)
GATA40.96
TBX50.89
KDM6A0.72
SMAD40.63
FOXH10.59
TBX20.59