cns inflammation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006082
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Genes

29 gene mutations causing the cns inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AIRE autoimmune regulator
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
C3 complement component 3
CD28 CD28 molecule
CD4 CD4 molecule
CX3CR1 chemokine (C-X3-C motif) receptor 1
CXCL10 chemokine (C-X-C motif) ligand 10
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
GALC galactosylceramidase
HEXB hexosaminidase B (beta polypeptide)
HLA-A major histocompatibility complex, class I, A
IFNB1 interferon, beta 1, fibroblast
IL4 interleukin 4
IL6 interleukin 6
LGALS3 lectin, galactoside-binding, soluble, 3
MAVS mitochondrial antiviral signaling protein
MFSD8 major facilitator superfamily domain containing 8
MGAT5B mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B
MMP2 matrix metallopeptidase 2
NLRP3 NLR family, pyrin domain containing 3
PPT1 palmitoyl-protein thioesterase 1
PRF1 perforin 1 (pore forming protein)
PSAP prosaposin
RNF128 ring finger protein 128, E3 ubiquitin protein ligase
SH3BP2 SH3-domain binding protein 2
SUMF1 sulfatase modifying factor 1
TBX21 T-box 21
TGFB1 transforming growth factor, beta 1