Gene: TRNV ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		0.400 GeneticVariation disease CLINVAR Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease. 25652200 2015
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		0.400 CausalMutation disease CLINVAR Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations. 20064630 2010
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		0.400 GeneticVariation disease CLINVAR Prevalence of mitochondrial DNA disease in adults. 17886296 2008
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		0.400 GeneticVariation disease CLINVAR Overexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNAVal carrying the pathogenic C25U mutation. 18400783 2008
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		0.400 CausalMutation disease CLINVAR Complex neurologic syndrome associated with the G1606A mutation of mitochondrial DNA. 12056939 2002
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		0.400 GeneticVariation disease CLINVAR Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation. 11799391 2002
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		0.400 CausalMutation disease CLINVAR A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentation. 9450773 1998
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		0.400 Biomarker disease CTD_human