Focal Seizures, Afebril Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C4049830
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Genes

25 genes associated with the disease Focal Seizures, Afebril in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARX aristaless related homeobox
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family)
CDKL5 cyclin-dependent kinase-like 5
CLCNKB chloride channel, voltage-sensitive Kb
FA2H fatty acid 2-hydroxylase
GABRG2 gamma-aminobutyric acid (GABA) A receptor, gamma 2
GNAO1 guanine nucleotide binding protein (G protein), alpha activating activity polypeptide O
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A
KCNA1 potassium channel, voltage gated shaker related subfamily A, member 1
MTOR mechanistic target of rapamycin (serine/threonine kinase)
NEUROD2 neuronal differentiation 2
PCDH19 protocadherin 19
PIGP phosphatidylinositol glycan anchor biosynthesis, class P
PIGQ phosphatidylinositol glycan anchor biosynthesis, class Q
PNKP polynucleotide kinase 3'-phosphatase
POLR3A polymerase (RNA) III (DNA directed) polypeptide A, 155kDa
PRRT2 proline-rich transmembrane protein 2
SCN2A sodium channel, voltage gated, type II alpha subunit
SIK1 salt-inducible kinase 1
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
SLC25A22 solute carrier family 25 (mitochondrial carrier: glutamate), member 22
SRPX2 sushi-repeat containing protein, X-linked 2
STXBP1 syntaxin binding protein 1
TRIM8 tripartite motif containing 8
TUBB3 tubulin, beta 3 class III