SCO2

Synonym(s): SCO1L

Locus: 22q13.33

Protein: Protein SCO2 homolog

Disorder(s):

• Mitochondrial Respiratory Chain Complex IV Deficiency (Nuclear Genes)
• Fatal Infantile Cardioencephalomyopathy due to Cytochrome c Oxidase Deficiency
• Leigh Syndrome (nuclear DNA mutation)