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GRIN2A
5 associated diseases
5 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Benign familial epilepsy of childhood with rolandic spikes
Early-onset epileptic encephalopathy and intellectual deficit due to GRIN2A mutation
Epileptic encephalopathy with continuous spike-and-wave during sleep
Landau-Kleffner syndrome
Rolandic epilepsy - speech dyspraxia
Gene symbol Score
(click on to see the evidence)
DLG30.96
GRIN10.93
AP4M10.63
ACTN10.62
CASK0.52