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FLASH GENE
Symbol COX2 contributors: mct/ - updated : 24-10-2012
HGNC name mitochondrially encoded cytochrome c oxidase II
HGNC id 7421
ASSOCIATED DISORDERS
corresponding disease(s) MELAS , MTENC3 , MTDFN1
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional germinal mutation      
in mitochondrial proximal myopathy with lactic acidosis (COX deficiency)
tumoral     --low  
in prostate tumor
Susceptibility to schizophrenia
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS