Gene: SCO2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.600 GeneticVariation disease LHGDN Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts. 11751685 2001
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.600 Biomarker disease MGD Contrariwise, treatment with the AMPK agonist AICAR led to partial correction of COX deficiency in all three models, and, importantly, significant motor improvement up to normal in the Sco2(KO/KI) mouse. 21723506 2011
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.600 Biomarker disease MGD Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2. 19837698 2010