Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.700 Biomarker disease GENOMICS_ENGLAND A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies. 25655951 2015
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.700 GeneticVariation disease UNIPROT Cooperation between COA6 and SCO2 in COX2 maturation during cytochrome c oxidase assembly links two mitochondrial cardiomyopathies. 25959673 2015
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.700 GeneticVariation disease UNIPROT Novel SCO2 mutation (G1521A) presenting as a spinal muscular atrophy type I phenotype. 14994243 2004
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.700 CausalMutation disease CLINVAR
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.700 Biomarker disease CTD_human Unexpected vascular enrichment of SCO1 over SCO2 in mammalian tissues: implications for human mitochondrial disease. 20864674 2010