Demyelinating Diseases Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

19 genes associated with the Demyelinating Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
CSGALNACT1 chondroitin sulfate N-acetylgalactosaminyltransferase 1
DHFR dihydrofolate reductase
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32)
FCGR3A Fc fragment of IgG, low affinity IIIa, receptor (CD16a)
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IL2RA interleukin 2 receptor, alpha
IL7R interleukin 7 receptor
MPZ myelin protein zero
MT-TK tRNA
MT-TL1 tRNA
MT-TL2 tRNA
MT-TQ tRNA
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
RNR2 RNA, ribosomal cluster 2
TREM2 triggering receptor expressed on myeloid cells 2
TYROBP TYRO protein tyrosine kinase binding protein