Basal Ganglia Diseases Gene Set

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

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

Symbol Name
ACE angiotensin I converting enzyme
AKT1 v-akt murine thymoma viral oncogene homolog 1
APOE apolipoprotein E
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
BDNF brain-derived neurotrophic factor
C9ORF72 chromosome 9 open reading frame 72
CAT catalase
COMT catechol-O-methyltransferase
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
GBA glucosidase, beta, acid
GPX1 glutathione peroxidase 1
GRIK3 glutamate receptor, ionotropic, kainate 3
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
MAOA monoamine oxidase A
MAOB monoamine oxidase B
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
SLC20A2 solute carrier family 20 (phosphate transporter), member 2
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
SOD2 superoxide dismutase 2, mitochondrial
TNF tumor necrosis factor
VEGFA vascular endothelial growth factor A