Acute Encephalopathy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1306587
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Genes

31 genes associated with the disease Acute Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACY1 aminoacylase 1
ADAR adenosine deaminase, RNA-specific
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
BCAT2 branched chain amino-acid transaminase 2, mitochondrial
BRAF B-Raf proto-oncogene, serine/threonine kinase
COG8 component of oligomeric golgi complex 8
CPT2 carnitine palmitoyltransferase 2
CXCL13 chemokine (C-X-C motif) ligand 13
CXCL8 chemokine (C-X-C motif) ligand 8
ENO2 enolase 2 (gamma, neuronal)
ERLEC1 endoplasmic reticulum lectin 1
GZMA granzyme A (granzyme 1, cytotoxic T-lymphocyte-associated serine esterase 3)
GZMB granzyme B (granzyme 2, cytotoxic T-lymphocyte-associated serine esterase 1)
IFNG interferon, gamma
IL10 interleukin 10
IL1B interleukin 1, beta
IL1RN interleukin 1 receptor antagonist
IL4 interleukin 4
IL6 interleukin 6
LIF leukemia inhibitory factor
MMP9 matrix metallopeptidase 9
PCCA propionyl CoA carboxylase, alpha polypeptide
PCCB propionyl CoA carboxylase, beta polypeptide
RANBP2 RAN binding protein 2
SCN1A sodium channel, voltage gated, type I alpha subunit
SCN2A sodium channel, voltage gated, type II alpha subunit
SLC19A3 solute carrier family 19 (thiamine transporter), member 3
SLC22A5 solute carrier family 22 (organic cation/carnitine transporter), member 5
SLC25A15 solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
SPP1 secreted phosphoprotein 1
TNF tumor necrosis factor