Gene: TRNT ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4576
Gene Symbol: TRNT
TRNT 		0.100 CausalMutation phenotype 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 		0.100 CausalMutation phenotype CLINVAR CO2-sensitive tRNA modification associated with human mitochondrial disease. 29760464 2018
Entrez Id: 4576
Gene Symbol: TRNT
TRNT 		0.100 CausalMutation phenotype 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 		0.100 CausalMutation phenotype CLINVAR Mitochondrial disorder associated with newborn cardiopulmonary arrest. 8511015 1993
Entrez Id: 4576
Gene Symbol: TRNT
TRNT 		0.100 Biomarker phenotype HPO