Epilepsy, Absence Gene Set

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

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

Symbol Name
CACNA1H calcium channel, voltage-dependent, T type, alpha 1H subunit
CACNA1I calcium channel, voltage-dependent, T type, alpha 1I subunit
CACNG3 calcium channel, voltage-dependent, gamma subunit 3
CHRM3 cholinergic receptor, muscarinic 3
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1
GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1
GABRA5 gamma-aminobutyric acid (GABA) A receptor, alpha 5
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
GABRG2 gamma-aminobutyric acid (GABA) A receptor, gamma 2
GRM4 glutamate receptor, metabotropic 4
INHA inhibin, alpha
KCNMB3 potassium channel subfamily M regulatory beta subunit 3
KHDRBS3 KH domain containing, RNA binding, signal transduction associated 3
LGI4 leucine-rich repeat LGI family, member 4
NIPA2 non imprinted in Prader-Willi/Angelman syndrome 2
OPRM1 opioid receptor, mu 1
PNPO pyridoxamine 5'-phosphate oxidase
SCN1A sodium channel, voltage gated, type I alpha subunit
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
VRK2 vaccinia related kinase 2
ZEB2 zinc finger E-box binding homeobox 2