Myoclonic Epilepsy, Juvenile Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D020190
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Genes

8 genes/proteins associated with the disease Myoclonic Epilepsy, Juvenile from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
EFHC1 EF-hand domain (C-terminal) containing 1 2.88009
EJM3 Epilepsy, juvenile myoclonic 3 2.88009
EJM2 epilepsy, juvenile myoclonic 2 2.88009
EJM4 Myoclonic epilepsy, juvenile, 4 2.88009
CLCN2 chloride channel, voltage-sensitive 2 2.88009
CACNB4 calcium channel, voltage-dependent, beta 4 subunit 2.88009
GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1 2.88009
JRK Jrk homolog (mouse) 2.88009