dyskinesia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A movement disorder which consists of effects including diminished voluntary movements and the presence of involuntary movements. (Human Phenotype Ontology, HP_0100660)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100660
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Genes

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

Symbol Name
ATXN7 ataxin 7
B4GALNT1 beta-1,4-N-acetyl-galactosaminyl transferase 1
C9ORF72 chromosome 9 open reading frame 72
CHMP2B charged multivesicular body protein 2B
DPYS dihydropyrimidinase
FGF14 fibroblast growth factor 14
FOXG1 forkhead box G1
PANK2 pantothenate kinase 2
PDGFB platelet-derived growth factor beta polypeptide
PNPT1 polyribonucleotide nucleotidyltransferase 1
PRRT2 proline-rich transmembrane protein 2
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SLC46A1 solute carrier family 46 (folate transporter), member 1
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
TSEN2 TSEN2 tRNA splicing endonuclease subunit
TSEN54 TSEN54 tRNA splicing endonuclease subunit
VPS13A vacuolar protein sorting 13 homolog A (S. cerevisiae)
VPS35 vacuolar protein sorting 35 homolog (S. cerevisiae)