Source: CURATED

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 1355
Gene Symbol: COX15
COX15 		cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		disease 0.740 limited 1.000 8 3 2002 2016
Entrez Id: 1355
Gene Symbol: COX15
COX15 		cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
CUI: C3554534
Disease: CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2
CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2 		disease 0.600 None 1.000 4 2 2003 2016
Entrez Id: 1355
Gene Symbol: COX15
COX15 		cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
CUI: C1858424
Disease: Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency 		disease 0.500 None 1.000 2 0 1990 2011
Entrez Id: 1355
Gene Symbol: COX15
COX15 		cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
CUI: C1850599
Disease: Leigh Syndrome due to Mitochondrial Complex IV Deficiency
Leigh Syndrome due to Mitochondrial Complex IV Deficiency 		disease 0.400 limited 1.000 6 3 2002 2015
Entrez Id: 1355
Gene Symbol: COX15
COX15 		cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
CUI: C0268237
Disease: Cytochrome-c Oxidase Deficiency
Cytochrome-c Oxidase Deficiency 		disease 0.330 None 1.000 0 0 2003 2005
Entrez Id: 1355
Gene Symbol: COX15
COX15 		cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
CUI: C1850597
Disease: Leigh Syndrome Due To Mitochondrial Complex II Deficiency
Leigh Syndrome Due To Mitochondrial Complex II Deficiency 		disease 0.300 limited 1.000 6 0 2002 2015
Entrez Id: 1355
Gene Symbol: COX15
COX15 		cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
CUI: C2931891
Disease: Necrotizing encephalopathy, infantile subacute, of Leigh
Necrotizing encephalopathy, infantile subacute, of Leigh 		disease 0.300 limited 1.000 6 0 2002 2015
Entrez Id: 1355
Gene Symbol: COX15
COX15 		cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
CUI: C1850600
Disease: Leigh Syndrome due to Mitochondrial Complex V Deficiency
Leigh Syndrome due to Mitochondrial Complex V Deficiency 		disease 0.300 limited 1.000 6 0 2002 2015
Entrez Id: 1355
Gene Symbol: COX15
COX15 		cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
CUI: C1850598
Disease: Leigh Syndrome due to Mitochondrial Complex III Deficiency
Leigh Syndrome due to Mitochondrial Complex III Deficiency 		disease 0.300 limited 1.000 6 0 2002 2015
Entrez Id: 1355
Gene Symbol: COX15
COX15 		cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
CUI: C1838951
Disease: LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY 		disease 0.300 limited 1.000 6 0 2002 2015
Entrez Id: 1355
Gene Symbol: COX15
COX15 		cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases 		group 0.300 strong 1.000 1 0 2016 2016
Entrez Id: 1355
Gene Symbol: COX15
COX15 		cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
CUI: C0751268
Disease: Encephalopathy, Subacute Necrotizing, Juvenile
Encephalopathy, Subacute Necrotizing, Juvenile 		disease 0.300 None 0 0
Entrez Id: 1355
Gene Symbol: COX15
COX15 		cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
CUI: C0751267
Disease: Encephalopathy, Subacute Necrotizing, Infantile
Encephalopathy, Subacute Necrotizing, Infantile 		disease 0.300 None 0 0