Myoclonic Epilepsies, Progressive Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D020191
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Genes

12 genes/proteins associated with the disease Myoclonic Epilepsies, Progressive from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SERPINI1 serpin peptidase inhibitor, clade I (neuroserpin), member 1 2.88009
NHLRC1 NHL repeat containing E3 ubiquitin protein ligase 1 2.88009
SACS sacsin molecular chaperone 2.88009
NEU1 sialidase 1 (lysosomal sialidase) 2.88009
ATN1 atrophin 1 2.88009
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin) 2.88009
CLN6 ceroid-lipofuscinosis, neuronal 6, late infantile, variant 2.88009
TSC1 tuberous sclerosis 1 2.88009
AFG3L2 AFG3-like AAA ATPase 2 2.88009
PRNP prion protein 2.88009
KCNC1 potassium channel, voltage gated Shaw related subfamily C, member 1 2.88009
TBC1D24 TBC1 domain family, member 24 2.88009