Convulsions Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0751494
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Genes

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

Symbol Name
ACP1 acid phosphatase 1, soluble
ALDH7A1 aldehyde dehydrogenase 7 family, member A1
CLCN6 chloride channel, voltage-sensitive 6
HP haptoglobin
IL33 interleukin 33
KAT5 K(lysine) acetyltransferase 5
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3
KCNQ5 potassium channel, voltage gated KQT-like subfamily Q, member 5
P2RX7 purinergic receptor P2X, ligand gated ion channel, 7
PLA2G4A phospholipase A2, group IVA (cytosolic, calcium-dependent)
SCN1A sodium channel, voltage gated, type I alpha subunit
SCN2A sodium channel, voltage gated, type II alpha subunit
SCN3A sodium channel, voltage gated, type III alpha subunit
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SLC12A5 solute carrier family 12 (potassium/chloride transporter), member 5
SLC13A5 solute carrier family 13 (sodium-dependent citrate transporter), member 5
SLC30A3 solute carrier family 30 (zinc transporter), member 3
STXBP1 syntaxin binding protein 1
SUOX sulfite oxidase