basal ganglia disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

31 genes involed in the disease basal ganglia disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ATP13A2 ATPase type 13A2
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
ATP6AP2 ATPase, H+ transporting, lysosomal accessory protein 2
ATXN2 ataxin 2
COQ2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
DCTN1 dynactin 1
DNAJC6 DnaJ (Hsp40) homolog, subfamily C, member 6
EIF4G1 eukaryotic translation initiation factor 4 gamma, 1
FBXO7 F-box protein 7
GBA glucosidase, beta, acid
GCH1 GTP cyclohydrolase 1
GIGYF2 GRB10 interacting GYF protein 2
GRN granulin
HTRA2 HtrA serine peptidase 2
LRRK2 leucine-rich repeat kinase 2
MAPT microtubule-associated protein tau
PARK2 parkin RBR E3 ubiquitin protein ligase
PARK7 parkinson protein 7
PINK1 PTEN induced putative kinase 1
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
SLC19A3 solute carrier family 19 (thiamine transporter), member 3
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SNCAIP synuclein, alpha interacting protein
SYNJ1 synaptojanin 1
TAF1 TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa
TH tyrosine hydroxylase
TRPM7 transient receptor potential cation channel, subfamily M, member 7
UCHL1 ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
VPS35 vacuolar protein sorting 35 homolog (S. cerevisiae)