Familial Benign Neonatal Epilepsy Gene Set
Genes
17 genes associated with the disease Familial Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ATP1A2
|
ATPase, Na+/K+ transporting, alpha 2 polypeptide
|
|
CHRNA4
|
cholinergic receptor, nicotinic, alpha 4 (neuronal)
|
|
CHRNA7
|
cholinergic receptor, nicotinic, alpha 7 (neuronal)
|
|
CSTB
|
cystatin B (stefin B)
|
|
EFHC1
|
EF-hand domain (C-terminal) containing 1
|
|
GALE
|
UDP-galactose-4-epimerase
|
|
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
|
|
MC3R
|
melanocortin 3 receptor
|
|
PRRT2
|
proline-rich transmembrane protein 2
|
|
SCN1A
|
sodium channel, voltage gated, type I alpha subunit
|
|
SCN1B
|
sodium channel, voltage gated, type I beta subunit
|
|
SCN2A
|
sodium channel, voltage gated, type II alpha subunit
|
|
SCN8A
|
sodium channel, voltage gated, type VIII alpha subunit
|
|
SLC5A11
|
solute carrier family 5 (sodium/inositol cotransporter), member 11
|
|
WASF2
|
WAS protein family, member 2
|
