Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.300 Biomarker group CTD_human COX19 mediates the transduction of a mitochondrial redox signal from SCO1 that regulates ATP7A-mediated cellular copper efflux. 23345593 2013
Entrez Id: 2348
Gene Symbol: FOLR1
FOLR1 		0.300 Biomarker group CTD_human Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed myelin metabolism. 19732866 2009
Entrez Id: 91942
Gene Symbol: NDUFAF2
NDUFAF2 		0.300 Biomarker group CTD_human A molecular chaperone for mitochondrial complex I assembly is mutated in a progressive encephalopathy. 16200211 2005
Entrez Id: 2752
Gene Symbol: GLUL
GLUL 		0.300 Biomarker group CTD_human Congenital glutamine deficiency with glutamine synthetase mutations. 16267323 2005