Epilepsy, Generalized 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:D004829
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18 genes/proteins associated with the disease Epilepsy, Generalized from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
JRK Jrk homolog (mouse) 2.88009
CACNB4 calcium channel, voltage-dependent, beta 4 subunit 2.88009
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal) 2.88009
SCN1A sodium channel, voltage gated, type I alpha subunit 2.88009
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.28703
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 1.25807
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) 1.23392
SLC1A1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 1.199
CYP2C19 cytochrome P450, family 2, subfamily C, polypeptide 19 1.17926
FOS FBJ murine osteosarcoma viral oncogene homolog 1.15089
BDNF brain-derived neurotrophic factor 1.11673
GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1 1.11186
CAT catalase 1.09611
JUN jun proto-oncogene 1.0561
BCL2 B-cell CLL/lymphoma 2 1.04868
SOD2 superoxide dismutase 2, mitochondrial 1.04831
NCL nucleolin 1.04163
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3 1.03976