Myoclonic Epilepsy, Juvenile Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

17 genes associated with the Myoclonic Epilepsy, Juvenile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
BRD2 bromodomain containing 2
CHRM3 cholinergic receptor, muscarinic 3
CHRNA4 cholinergic receptor, nicotinic, alpha 4 (neuronal)
CLOCK clock circadian regulator
EFHC1 EF-hand domain (C-terminal) containing 1
GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1
GABRA6 gamma-aminobutyric acid (GABA) A receptor, alpha 6
GABRB2 gamma-aminobutyric acid (GABA) A receptor, beta 2
GABRG2 gamma-aminobutyric acid (GABA) A receptor, gamma 2
GRM4 glutamate receptor, metabotropic 4
PER2 period circadian clock 2
PER3 period circadian clock 3
PNPO pyridoxamine 5'-phosphate oxidase
SCN1A sodium channel, voltage gated, type I alpha subunit
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)
VRK2 vaccinia related kinase 2
ZEB2 zinc finger E-box binding homeobox 2