Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4576
Gene Symbol: TRNT
TRNT
CUI: C0036572
Disease: Seizures
Seizures 		0.100 CausalMutation CLINVAR Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype. 30236074

2018
Entrez Id: 4576
Gene Symbol: TRNT
TRNT
CUI: C0036572
Disease: Seizures
Seizures 		0.100 CausalMutation CLINVAR CO2-sensitive tRNA modification associated with human mitochondrial disease. 29760464

2018
Entrez Id: 4576
Gene Symbol: TRNT
TRNT
CUI: C0036572
Disease: Seizures
Seizures 		0.100 CausalMutation CLINVAR New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset. 22638997

2012
Entrez Id: 4576
Gene Symbol: TRNT
TRNT
CUI: C0036572
Disease: Seizures
Seizures 		0.100 CausalMutation CLINVAR Mitochondrial disorder associated with newborn cardiopulmonary arrest. 8511015

1993
Entrez Id: 4576
Gene Symbol: TRNT
TRNT
CUI: C0036572
Disease: Seizures
Seizures 		0.100 Biomarker HPO