Myoclonus Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Very brief, involuntary random muscular contractions occurring at rest, in response to sensory stimuli, or accompanying voluntary movements. (Human Phenotype Ontology, HP_0001336)
External Link https://www.disgenet.org/browser/0/1/0/C0585540
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Genes

3 genes associated with the disease Myoclonus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
GOSR2 golgi SNAP receptor complex member 2
KIF5A kinesin family member 5A
NOL3 nucleolar protein 3 (apoptosis repressor with CARD domain)