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RYR1
7 associated diseases
6 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Autosomal dominant centronuclear myopathy
Benign Samaritan congenital myopathy
Central core disease
Congenital multicore myopathy with external ophthalmoplegia
King-Denborough syndrome
Malignant hyperthermia
Moderate multiminicore disease with hand involvement
Gene symbol Score
(click on to see the evidence)
TRDN0.9
RYR20.73
TF0.63
TTN0.63
CACNA1S0.62
CALM10.52