seizures Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description Seizures are an intermittent abnormality of the central nervous system due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements. The term epilepsy is used to describe chronic, recurrent seizures. (Human Phenotype Ontology, HP_0001250)
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Genes

134 genes co-occuring with the biological term seizures in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ABCC2 ATP-binding cassette, sub-family C (CFTR/MRP), member 2
ACP2 acid phosphatase 2, lysosomal
ADGRV1 adhesion G protein-coupled receptor V1
ADORA1 adenosine A1 receptor
ADORA2A adenosine A2a receptor
AGER advanced glycosylation end product-specific receptor
ALDH7A1 aldehyde dehydrogenase 7 family, member A1
ANKH ANKH inorganic pyrophosphate transport regulator
APOE apolipoprotein E
APP amyloid beta (A4) precursor protein
AQP4 aquaporin 4
ARX aristaless related homeobox
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
ATPIF1 ATPase inhibitory factor 1
AUH AU RNA binding protein/enoyl-CoA hydratase
BDNF brain-derived neurotrophic factor
C12ORF57 chromosome 12 open reading frame 57
C3 complement component 3
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CACNA1H calcium channel, voltage-dependent, T type, alpha 1H subunit
CACNA2D2 calcium channel, voltage-dependent, alpha 2/delta subunit 2
CASP1 caspase 1, apoptosis-related cysteine peptidase
CC2D2A coiled-coil and C2 domain containing 2A
CDKL5 cyclin-dependent kinase-like 5
CHD2 chromodomain helicase DNA binding protein 2
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal)
CLIC4 chloride intracellular channel 4
CLN8 ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
COX20 COX20 cytochrome c oxidase assembly factor
CPA6 carboxypeptidase A6
CREB1 cAMP responsive element binding protein 1
CXCL8 chemokine (C-X-C motif) ligand 8
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
DEL17Q12 Chromosome 17q12 deletion syndrome
DGKD diacylglycerol kinase, delta 130kDa
ELP4 elongator acetyltransferase complex subunit 4
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
FBXO28 F-box protein 28
FIG4 FIG4 phosphoinositide 5-phosphatase
FLNA filamin A, alpha
FMR1 fragile X mental retardation 1
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1
GABRA4 gamma-aminobutyric acid (GABA) A receptor, alpha 4
GABRA6 gamma-aminobutyric acid (GABA) A receptor, alpha 6
GABRB1 gamma-aminobutyric acid (GABA) A receptor, beta 1
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
GABRG2 gamma-aminobutyric acid (GABA) A receptor, gamma 2
GAD1 glutamate decarboxylase 1 (brain, 67kDa)
GFAP glial fibrillary acidic protein
GIPC3 GIPC PDZ domain containing family, member 3
GLUL glutamate-ammonia ligase
GPHN gephyrin
HCN1 hyperpolarization activated cyclic nucleotide gated potassium channel 1
HCN2 hyperpolarization activated cyclic nucleotide gated potassium channel 2
HLA-B major histocompatibility complex, class I, B
HMGB1 high mobility group box 1
HNRNPU heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A)
HNRNPU-AS1 HNRNPU antisense RNA 1
HP haptoglobin
HTT huntingtin
IDH1 isocitrate dehydrogenase 1 (NADP+), soluble
IFNA1 interferon, alpha 1
IL10 interleukin 10
IL17A interleukin 17A
IL17RA interleukin 17 receptor A
IL18 interleukin 18
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
IL1RN interleukin 1 receptor antagonist
IL6 interleukin 6
IMPA2 inositol(myo)-1(or 4)-monophosphatase 2
INSR insulin receptor
IQSEC2 IQ motif and Sec7 domain 2
KCND2 potassium channel, voltage gated Shal related subfamily D, member 2
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2
KCNH3 potassium channel, voltage gated eag related subfamily H, member 3
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3
KCNT1 potassium channel, sodium activated subfamily T, member 1
KPTN kaptin (actin binding protein)
LAMB1 laminin, beta 1
LGI1 leucine-rich, glioma inactivated 1
MBD5 methyl-CpG binding domain protein 5
MECP2 methyl CpG binding protein 2
MEF2C myocyte enhancer factor 2C
MIR196B microRNA 196b
MMP8 matrix metallopeptidase 8
MMP9 matrix metallopeptidase 9
MPDZ multiple PDZ domain protein
MUSK muscle, skeletal, receptor tyrosine kinase
NHLRC1 NHL repeat containing E3 ubiquitin protein ligase 1
OPRM1 opioid receptor, mu 1
PAX6 paired box 6
PCDH19 protocadherin 19
PLCB1 phospholipase C, beta 1 (phosphoinositide-specific)
PNKP polynucleotide kinase 3'-phosphatase
PNPO pyridoxamine 5'-phosphate oxidase
POLG polymerase (DNA directed), gamma
PPARG peroxisome proliferator-activated receptor gamma
PRICKLE1 prickle homolog 1 (Drosophila)
PRRT2 proline-rich transmembrane protein 2
PSEN1 presenilin 1
PTEN phosphatase and tensin homolog
PURA purine-rich element binding protein A
S100B S100 calcium binding protein B
SCN1A sodium channel, voltage gated, type I alpha subunit
SCN1B sodium channel, voltage gated, type I beta subunit
SCN2A sodium channel, voltage gated, type II alpha subunit
SCN3A sodium channel, voltage gated, type III alpha subunit
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SCN9A sodium channel, voltage gated, type IX alpha subunit
SGCE sarcoglycan, epsilon
SGK1 serum/glucocorticoid regulated kinase 1
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SLC12A5 solute carrier family 12 (potassium/chloride transporter), member 5
SLC1A3 solute carrier family 1 (glial high affinity glutamate transporter), member 3
SLC25A22 solute carrier family 25 (mitochondrial carrier: glutamate), member 22
SLC29A1 solute carrier family 29 (equilibrative nucleoside transporter), member 1
SLC6A19 solute carrier family 6 (neutral amino acid transporter), member 19
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A8 solute carrier family 6 (neurotransmitter transporter), member 8
SYT14 synaptotagmin XIV
SZT2 seizure threshold 2 homolog (mouse)
TBC1D24 TBC1 domain family, member 24
TIMP1 TIMP metallopeptidase inhibitor 1
TIMP4 TIMP metallopeptidase inhibitor 4
TNF tumor necrosis factor
TPP1 tripeptidyl peptidase I
TSPEAR thrombospondin-type laminin G domain and EAR repeats
UCHL1 ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
VSNL1 visinin-like 1