Meningoencephalitis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A central nervous system disease that involves encephalitis which occurs along with meningitis. (Human Disease Ontology, DOID_10554)
External Link https://www.disgenet.org/browser/0/1/0/C0025309
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Genes

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

Symbol Name
AIF1 allograft inflammatory factor 1
AQP4 aquaporin 4
CARD9 caspase recruitment domain family, member 9
CAT catalase
CD40LG CD40 ligand
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
CSNK2A1 casein kinase 2, alpha 1 polypeptide
CXCL13 chemokine (C-X-C motif) ligand 13
DDX58 DEAD (Asp-Glu-Ala-Asp) box polypeptide 58
ENO2 enolase 2 (gamma, neuronal)
GFAP glial fibrillary acidic protein
IFNG interferon, gamma
IFNL3 interferon, lambda 3
IGF2R insulin-like growth factor 2 receptor
IL10 interleukin 10
IL6 interleukin 6
LAMC2 laminin, gamma 2
MAPT microtubule-associated protein tau
MOG myelin oligodendrocyte glycoprotein
MT-CYB cytochrome b
OCLN occludin
PLAT plasminogen activator, tissue
PPIG peptidylprolyl isomerase G (cyclophilin G)
PTX3 pentraxin 3, long
RARRES3 retinoic acid receptor responder (tazarotene induced) 3
ROBO3 roundabout, axon guidance receptor, homolog 3 (Drosophila)
SIRT1 sirtuin 1
SLC9B1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1
TLR8 toll-like receptor 8
TNF tumor necrosis factor