Gene: TK2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7084
Gene Symbol: TK2
TK2 		0.110 GeneticVariation disease BEFREE In patients, TK2 mutations typically manifest as a rapidly progressive myopathy with infantile onset, leading to respiratory insufficiency and encephalopathy in the most severe clinical presentations. 31351931 2019
Entrez Id: 7084
Gene Symbol: TK2
TK2 		0.110 Biomarker disease HPO