status epilepticus Gene Set
Genes
23 genes associated with the status epilepticus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ALDH5A1
|
aldehyde dehydrogenase 5 family, member A1
|
|
ALDH7A1
|
aldehyde dehydrogenase 7 family, member A1
|
|
AMACR
|
alpha-methylacyl-CoA racemase
|
|
C10ORF2
|
chromosome 10 open reading frame 2
|
|
CHD2
|
chromodomain helicase DNA binding protein 2
|
|
COG8
|
component of oligomeric golgi complex 8
|
|
CTSD
|
cathepsin D
|
|
FH
|
fumarate hydratase
|
|
FIG4
|
FIG4 phosphoinositide 5-phosphatase
|
|
GABRA1
|
gamma-aminobutyric acid (GABA) A receptor, alpha 1
|
|
KCNT1
|
potassium channel, sodium activated subfamily T, member 1
|
|
PCDH19
|
protocadherin 19
|
|
PDSS2
|
prenyl (decaprenyl) diphosphate synthase, subunit 2
|
|
POLG
|
polymerase (DNA directed), gamma
|
|
PRODH
|
proline dehydrogenase (oxidase) 1
|
|
QARS
|
glutaminyl-tRNA synthetase
|
|
SCN1A
|
sodium channel, voltage gated, type I alpha subunit
|
|
SCN2A
|
sodium channel, voltage gated, type II alpha subunit
|
|
SLC13A5
|
solute carrier family 13 (sodium-dependent citrate transporter), member 5
|
|
ST3GAL5
|
ST3 beta-galactoside alpha-2,3-sialyltransferase 5
|
|
STXBP1
|
syntaxin binding protein 1
|
|
TBC1D24
|
TBC1 domain family, member 24
|
|
UPB1
|
ureidopropionase, beta
|
