Symptomatic Myoclonic Epilepsy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0338479
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Genes

8 genes associated with the disease Symptomatic Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
PMP22 peripheral myelin protein 22
POMC proopiomelanocortin
RAPGEF2 Rap guanine nucleotide exchange factor (GEF) 2
SAMD12 sterile alpha motif domain containing 12
SCN1A sodium channel, voltage gated, type I alpha subunit
SCN9A sodium channel, voltage gated, type IX alpha subunit
STXBP1 syntaxin binding protein 1
TNRC6A trinucleotide repeat containing 6A