Gene: COX15 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1355
Gene Symbol: COX15
COX15 		0.300 Biomarker disease CLINGEN Opa1 overexpression ameliorates the phenotype of two mitochondrial disease mouse models. 26039449 2015
Entrez Id: 1355
Gene Symbol: COX15
COX15 		0.300 Biomarker disease CLINGEN Proteomics. Tissue-based map of the human proteome. 25613900 2015
Entrez Id: 1355
Gene Symbol: COX15
COX15 		0.300 Biomarker disease CLINGEN In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis. 21723506 2011
Entrez Id: 1355
Gene Symbol: COX15
COX15 		0.300 Biomarker disease CLINGEN Functional and genetic studies demonstrate that mutation in the COX15 gene can cause Leigh syndrome. 15235026 2004
Entrez Id: 1355
Gene Symbol: COX15
COX15 		0.300 Biomarker disease CLINGEN Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy. 12474143 2003
Entrez Id: 1355
Gene Symbol: COX15
COX15 		0.300 Biomarker disease CLINGEN Mitochondrial ferredoxin is required for heme A synthesis in Saccharomyces cerevisiae. 11788607 2002