Benign Neonatal 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/C0270851
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Genes

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

Symbol Name
KCNA1 potassium channel, voltage gated shaker related subfamily A, member 1
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3
KCNQ5 potassium channel, voltage gated KQT-like subfamily Q, member 5
MC3R melanocortin 3 receptor
PRRT2 proline-rich transmembrane protein 2