Cytoscape Web
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FKTN
5 associated diseases
1 protein interaction
UniProt info -
OMIM info -
Disease ODCs link
Autosomal recessive limb-girdle muscular dystrophy type 2M
Congenital muscular dystrophy without intellectual disability
Familial isolated dilated cardiomyopathy
Muscle-eye-brain disease
Walker-Warburg syndrome
Gene symbol Score
(click on to see the evidence)
CNBP0.63