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RRM2B
5 associated diseases
4 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
Autosomal dominant progressive external ophthalmoplegia
Kearns-Sayre syndrome
Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
Mitochondrial neurogastrointestinal encephalomyopathy
Gene symbol Score
(click on to see the evidence)
TP530.87
MDM20.77
ATM0.72
AICDA0.63