Atypical Parkinsonism Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C4302185
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Genes

30 genes associated with the disease Atypical Parkinsonism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APOE apolipoprotein E
ATP13A2 ATPase type 13A2
ATXN2 ataxin 2
ATXN3 ataxin 3
ATXN8 ataxin 8
BPIFA2 BPI fold containing family A, member 2
C9ORF72 chromosome 9 open reading frame 72
CIT citron rho-interacting serine/threonine kinase
CSF1R colony stimulating factor 1 receptor
FMR1 fragile X mental retardation 1
GRN granulin
LGALS1 lectin, galactoside-binding, soluble, 1
LRRK2 leucine-rich repeat kinase 2
LY6E lymphocyte antigen 6 complex, locus E
MAPT microtubule-associated protein tau
MSMB microseminoprotein, beta-
PARK2 parkin RBR E3 ubiquitin protein ligase
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
PRNP prion protein
PSPH phosphoserine phosphatase
PSPN persephin
REG1A regenerating islet-derived 1 alpha
RIDA reactive intermediate imine deaminase A homolog
SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1
SNCA synuclein, alpha (non A4 component of amyloid precursor)
STXBP3 syntaxin binding protein 3
SYNJ1 synaptojanin 1
TBP TATA box binding protein
VPS26A vacuolar protein sorting 26 homolog A (S. pombe)
VPS35 vacuolar protein sorting 35 homolog (S. cerevisiae)