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 CO2-sensitive tRNA modification associated with human mitochondrial disease. 29760464 2018
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 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: 57096
Gene Symbol: RPGRIP1
RPGRIP1 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 2776
Gene Symbol: GNAQ
GNAQ 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 1261
Gene Symbol: CNGA3
CNGA3 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 10002
Gene Symbol: NR2E3
NR2E3 		0.100 CausalMutation phenotype CLINVAR