parkinsons disease Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A progressive, degenerative neurologic disease characterized by a TREMOR that is maximal at rest, retropulsion (i.e. a tendency to fall backwards), rigidity, stooped posture, slowness of voluntary movements, and a masklike facial expression. Pathologic features include loss of melanin containing neurons in the substantia nigra and other pigmented nuclei of the brainstem. LEWY BODIES are present in the substantia nigra and locus coeruleus but may also be found in a related condition (LEWY BODY DISEASE, DIFFUSE) characterized by dementia in combination with varying degrees of parkinsonism. (Adams et al., Principles of Neurology, 6th ed, p1059, pp1067-75)|A neurodegenerative disease that results_from degeneration of the central nervous system that often impairs the sufferer's motor skills, speech, and other functions. (Experimental Factor Ontology, EFO_0002508)
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Genes

8 genes associated with the disease parkinsons disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
BDNF brain-derived neurotrophic factor
GSK3B glycogen synthase kinase 3 beta
GSTO2 glutathione S-transferase omega 2
LRRK2 leucine-rich repeat kinase 2
MAPT microtubule-associated protein tau
PARK2 parkin RBR E3 ubiquitin protein ligase
PINK1 PTEN induced putative kinase 1
SNCA synuclein, alpha (non A4 component of amyloid precursor)