Source: CLINGEN

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 6 0 2002 2016
Entrez Id: 1355
Gene Symbol: COX15
COX15
cytochrome c oxidase assembly homolog COX15 0.638 0.538 1.1E-13
Leigh Syndrome due to Mitochondrial Complex IV Deficiency
disease 0.400 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
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
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
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
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
Necrotizing encephalopathy, infantile subacute, of Leigh
disease 0.300 limited 1.000 6 0 2002 2015