encephalitis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Encephalitis is a nervous system infectious disease characterized as an acute inflammation of the brain. The usual cause is a viral infection, but bacteria can also cause it. Cases can range from mild to severe. For mild cases, you could have flu-like symptoms. Serious cases can cause severe headache, sudden fever, drowsiness, vomiting, confusion and seizures. (Human Disease Ontology, DOID_9588)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002383
Similar Terms
Downloads & Tools

Genes

26 genes associated with the encephalitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMACR alpha-methylacyl-CoA racemase
ATRX alpha thalassemia/mental retardation syndrome X-linked
BTK Bruton agammaglobulinemia tyrosine kinase
C4A complement component 4A (Rodgers blood group)
CIITA class II, major histocompatibility complex, transactivator
GCDH glutaryl-CoA dehydrogenase
HLA-B major histocompatibility complex, class I, B
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
IL10 interleukin 10
IL12RB2 interleukin 12 receptor, beta 2
IL23R interleukin 23 receptor
L2HGDH L-2-hydroxyglutarate dehydrogenase
LBR lamin B receptor
MEFV Mediterranean fever
NOD2 nucleotide-binding oligomerization domain containing 2
PRF1 perforin 1 (pore forming protein)
RFX5 regulatory factor X, 5 (influences HLA class II expression)
RFXANK regulatory factor X-associated ankyrin-containing protein
RFXAP regulatory factor X-associated protein
SH2D1A SH2 domain containing 1A
SLC6A19 solute carrier family 6 (neutral amino acid transporter), member 19
STAT4 signal transducer and activator of transcription 4
TLR4 toll-like receptor 4
TMEM70 transmembrane protein 70
WAS Wiskott-Aldrich syndrome
WIPF1 WAS/WASL interacting protein family, member 1