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C10ORF2
4 associated diseases
3 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Autosomal dominant progressive external ophthalmoplegia
Infantile onset spinocerebellar ataxia
Mitochondrial DNA depletion syndrome, hepatocerebrorenal form
Sensory ataxic neuropathy - dysarthria - ophthalmoparesis
Gene symbol Score
(click on to see the evidence)
SQSTM10.72
SMAD90.63
TP530.63