Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 84705
Gene Symbol: GTPBP3
GTPBP3 		0.700 GeneticVariation disease UNIPROT A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies. 26741492 2016
Entrez Id: 84705
Gene Symbol: GTPBP3
GTPBP3 		0.700 GeneticVariation disease UNIPROT Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy. 25434004 2014
Entrez Id: 84705
Gene Symbol: GTPBP3
GTPBP3 		0.700 GermlineCausalMutation disease ORPHANET Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy. 25434004 2014
Entrez Id: 84705
Gene Symbol: GTPBP3
GTPBP3 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy. 25434004 2014
Entrez Id: 84705
Gene Symbol: GTPBP3
GTPBP3 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 84705
Gene Symbol: GTPBP3
GTPBP3 		0.700 Biomarker disease CTD_human
Entrez Id: 84705
Gene Symbol: GTPBP3
GTPBP3 		0.700 CausalMutation disease CLINVAR
Entrez Id: 84705
Gene Symbol: GTPBP3
GTPBP3 		0.700 GeneticVariation disease CLINVAR