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DES
5 associated diseases
9 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Autosomal dominant limb-girdle muscular dystrophy type 1E
Autosomal recessive limb-girdle muscular dystrophy due to desmin deficiency
Desminopathy
Familial isolated dilated cardiomyopathy
Scapuloperoneal amyotrophy
Gene symbol Score
(click on to see the evidence)
MTM10.79
DSP0.78
MLH10.78
NEB0.75
PKD10.74
DYSF0.65
CRYAB0.56
HADHB0.49
JUP0.49