Gene: TTC19 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54902
Gene Symbol: TTC19
TTC19 		0.310 GeneticVariation group BEFREE TTC19 mutations constitute a rare cause of CIII deficiency and are associated with neurological disorders in childhood and adulthood. 25652355 2015
Entrez Id: 54902
Gene Symbol: TTC19
TTC19 		0.310 Biomarker group CTD_human Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies. 21278747 2011