dyskinesia Gene Set

Dataset GWASdb SNP-Phenotype 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://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0100660
Similar Terms
Downloads & Tools

Genes

8 genes associated with the dyskinesia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
RYR1 ryanodine receptor 1 (skeletal) 1.03063
C14ORF39 chromosome 14 open reading frame 39 0.859494
LARGE like-glycosyltransferase 0.797753
PCSK2 proprotein convertase subtilisin/kexin type 2 0.776085
MDGA2 MAM domain containing glycosylphosphatidylinositol anchor 2 0.666055
TBC1D22A TBC1 domain family, member 22A 0.636183
GLI2 GLI family zinc finger 2 0.633071
EEPD1 endonuclease/exonuclease/phosphatase family domain containing 1 0.608153