Myoclonus Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Very brief, involuntary random muscular contractions occurring at rest, in response to sensory stimuli, or accompanying voluntary movements. (Human Phenotype Ontology, HP_0001336)
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7 genes associated with the Myoclonus phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
GCH1 GTP cyclohydrolase 1
NKX2-1 NK2 homeobox 1
PRNP prion protein
SGCE sarcoglycan, epsilon
THAP1 THAP domain containing, apoptosis associated protein 1
TOR1A torsin family 1, member A (torsin A)