Epilepsy, Benign Neonatal Gene Set

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

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

Symbol Name
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3
LGI4 leucine-rich repeat LGI family, member 4
PRRT2 proline-rich transmembrane protein 2
SCN2A sodium channel, voltage gated, type II alpha subunit