Cytoscape Web
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MT-CO1
7 associated diseases
6 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Genetic recurrent myoglobinuria
Isolated cytochrome C oxidase deficiency
Leber hereditary optic neuropathy
Maternally-inherited Leigh syndrome
MELAS syndrome
Mitochondrial nonsyndromic sensorineural deafness
Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure
Gene symbol Score
(click on to see the evidence)
COX140.82
LIG40.63
MT-CO20.63
NDUFA90.58
HSPD10.55
SNCA0.49