Benign Rolandic Epilepsy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C2363129
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Genes

14 genes associated with the disease Benign Rolandic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARSA arylsulfatase A
BDNF brain-derived neurotrophic factor
CDK2 cyclin-dependent kinase 2
CHRNA4 cholinergic receptor, nicotinic, alpha 4 (neuronal)
ELP4 elongator acetyltransferase complex subunit 4
FMR1 fragile X mental retardation 1
GABRG2 gamma-aminobutyric acid (GABA) A receptor, gamma 2
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3
PRRT2 proline-rich transmembrane protein 2
RBFOX1 RNA binding protein, fox-1 homolog (C. elegans) 1
SRPX2 sushi-repeat containing protein, X-linked 2
TP53 tumor protein p53