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 		0.600 GeneticVariation disease UNIPROT Missense mutation in the transcription factor NKX2-5: a novel molecular event in the pathogenesis of thyroid dysgenesis. 16418214 2006
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5 		0.600 Biomarker disease GENOMICS_ENGLAND Missense mutation in the transcription factor NKX2-5: a novel molecular event in the pathogenesis of thyroid dysgenesis. 16418214 2006
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5 		0.600 Biomarker disease CTD_human
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5 		0.600 Biomarker disease GENOMICS_ENGLAND