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MFN2
5 associated diseases
4 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Autosomal dominant Charcot-Marie-Tooth disease type 2A2
Autosomal dominant optic atrophy plus syndrome
Hereditary motor and sensory neuropathy type 5
Hereditary motor and sensory neuropathy type 6
Severe early-onset axonal neuropathy due to MFN2 deficiency
Gene symbol Score
(click on to see the evidence)
PARK20.74
LRRK20.65
HUWE10.63
VCP0.63