postural instability Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002172
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Genes

17 genes associated with the postural instability phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP13A2 ATPase type 13A2
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
ATXN2 ataxin 2
ATXN3 ataxin 3
COQ2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
CSF1R colony stimulating factor 1 receptor
DNAJC6 DnaJ (Hsp40) homolog, subfamily C, member 6
FBXO7 F-box protein 7
GIGYF2 GRB10 interacting GYF protein 2
LRRK2 leucine-rich repeat kinase 2
PARK2 parkin RBR E3 ubiquitin protein ligase
PINK1 PTEN induced putative kinase 1
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
SLC20A2 solute carrier family 20 (phosphate transporter), member 2
SLC30A10 solute carrier family 30, member 10
SYNJ1 synaptojanin 1
VPS35 vacuolar protein sorting 35 homolog (S. cerevisiae)