Brain Diseases Gene Set

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

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

Symbol Name
APOBEC3A apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3A
APOBEC3B apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3B
APOE apolipoprotein E
COL4A1 collagen, type IV, alpha 1
CRHR1 corticotropin releasing hormone receptor 1
CST3 cystatin C
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
EIF2B1 eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa
EIF2B2 eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
EIF2B3 eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa
EIF2B4 eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa
EIF2B5 eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
GSTM1 glutathione S-transferase mu 1
GSTT1 glutathione S-transferase theta 1
HMOX1 heme oxygenase 1
JAG1 jagged 1
LTA lymphotoxin alpha
MAPT microtubule-associated protein tau
MECP2 methyl CpG binding protein 2
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NRXN3 neurexin 3
POMT1 protein-O-mannosyltransferase 1
POMT2 protein-O-mannosyltransferase 2
PON1 paraoxonase 1
TREM2 triggering receptor expressed on myeloid cells 2
TYROBP TYRO protein tyrosine kinase binding protein