Atypical Absence Seizure Gene Set
Genes
17 genes associated with the disease Atypical Absence Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
CHD2
|
chromodomain helicase DNA binding protein 2
|
|
CUX2
|
cut-like homeobox 2
|
|
CYP17A1
|
cytochrome P450, family 17, subfamily A, polypeptide 1
|
|
DNM1
|
dynamin 1
|
|
EPM2A
|
epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
|
|
GABRB3
|
gamma-aminobutyric acid (GABA) A receptor, beta 3
|
|
GABRG2
|
gamma-aminobutyric acid (GABA) A receptor, gamma 2
|
|
GRIN2A
|
glutamate receptor, ionotropic, N-methyl D-aspartate 2A
|
|
KCNT2
|
potassium channel, sodium activated subfamily T, member 2
|
|
MAPK10
|
mitogen-activated protein kinase 10
|
|
NHLRC1
|
NHL repeat containing E3 ubiquitin protein ligase 1
|
|
PCDH19
|
protocadherin 19
|
|
PIGM
|
phosphatidylinositol glycan anchor biosynthesis, class M
|
|
SCN1A
|
sodium channel, voltage gated, type I alpha subunit
|
|
SCN1B
|
sodium channel, voltage gated, type I beta subunit
|
|
SHANK3
|
SH3 and multiple ankyrin repeat domains 3
|
|
SRPX2
|
sushi-repeat containing protein, X-linked 2
|
