akinesia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Inability to initiate changes in activity or movement and to perform ordinary volitional movements rapidly and easily. (Human Phenotype Ontology, HP_0002304)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002304
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Genes

10 genes associated with the akinesia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP13A2 ATPase type 13A2
CHRNA1 cholinergic receptor, nicotinic, alpha 1 (muscle)
CHRND cholinergic receptor, nicotinic, delta (muscle)
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
CNTN1 contactin 1
ERBB3 erb-b2 receptor tyrosine kinase 3
GBA glucosidase, beta, acid
MAPT microtubule-associated protein tau
PANK2 pantothenate kinase 2
VPS35 vacuolar protein sorting 35 homolog (S. cerevisiae)