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Browse result for Epilepsy

※ introduction

    A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.

Reference
DiseaseOntology: Epilepsy


PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD00278P111666513
SLC2A1
Solute carrier family 2, facilitated glucose transporter member 1
Homo sapiens
PTMD01001Q132242904
GRIN2B
Glutamate receptor ionotropic, NMDA 2B
Homo sapiens
PTMD00774Q96MT314416
PRICKLE1
Prickle-like protein 1
Homo sapiens
PTMD01380O951808912
CACNA1H
Voltage-dependent T-type calcium channel subunit alpha-1H
Homo sapiens
PTMD01577P284722562
GABRB3
Gamma-aminobutyric acid receptor subunit beta-3 receptor subunit beta-3)
Homo sapiens
PTMD01090P354986323
SCN1A
Sodium channel protein type 1 subunit alpha
Homo sapiens
PTMD01734Q128792903
GRIN2A
Glutamate receptor ionotropic, NMDA 2A
Homo sapiens
PTMD01386A6NL8872995
SHISA7
Protein shisa-7 receptor auxiliary subunit Shisa7)
Homo sapiens
PTMD02935O6074134898
HCN1
Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1
Homo sapiens
PTMD03015O751409681
DEPDC5
GATOR1 complex protein DEPDC5
Homo sapiens
PTMD03310O9490311212
PLPBP
Pyridoxal phosphate homeostasis protein
Homo sapiens
PTMD03404O952787957
EPM2A
Laforin
Homo sapiens
PTMD03554O959709211
LGI1
Leucine-rich glioma-inactivated protein 1
Homo sapiens
PTMD03707P040801476
CSTB
Cystatin-B
Homo sapiens
PTMD04330P176006853
SYN1
Synapsin-1
Homo sapiens
PTMD04361P185072566
GABRG2
Gamma-aminobutyric acid receptor subunit gamma-2 receptor subunit gamma-2)
Homo sapiens
PTMD04520P2246651083
GAL
Galanin peptides [Cleaved into: Galanin; Galanin message-associated peptide ]
Homo sapiens
PTMD04889P349032556
GABRA3
Gamma-aminobutyric acid receptor subunit alpha-3 receptor subunit alpha-3)
Homo sapiens
PTMD05051P41180846
CASR
Extracellular calcium-sensing receptor
Homo sapiens
PTMD05302P49419501
ALDH7A1
Alpha-aminoadipic semialdehyde dehydrogenase
Homo sapiens
PTMD05457P517881181
CLCN2
Chloride channel protein 2
Homo sapiens
PTMD05977P785095649
RELN
Reelin
Homo sapiens
PTMD06148Q022466900
CNTN2
Contactin-2
Homo sapiens
PTMD06186Q0325284823
LMNB2
Lamin-B2
Homo sapiens
PTMD06427Q129808131
NPRL3
GATOR1 complex protein NPRL3
Homo sapiens
PTMD06568Q13510427
ASAH1
Acid ceramidase [Cleaved into: Acid ceramidase subunit alpha; Acid ceramidase subunit beta]
Homo sapiens
PTMD06630Q138136709
SPTAN1
Spectrin alpha chain, non-erythrocytic 1
Homo sapiens
PTMD06948Q153826009
RHEB
GTP-binding protein Rheb
Homo sapiens
PTMD07620Q5JUK357582
KCNT1
Potassium channel subfamily T member 1
Homo sapiens
PTMD07629Q5JVL411432
EFHC1
EF-hand domain-containing protein 1
Homo sapiens
PTMD08792Q7Z3G616633
PRICKLE2
Prickle-like protein 2
Homo sapiens
PTMD09915Q8NB9016637
AFG2A
ATPase family gene 2 protein homolog A
Homo sapiens
PTMD10495Q8WTW410641
NPRL2
GATOR1 complex protein NPRL2
Homo sapiens
PTMD10808Q927961741
DLG3
Disks large homolog 3
Homo sapiens
PTMD11465Q96L7364324
NSD1
Histone-lysine N-methyltransferase, H3 lysine-36 specific
Homo sapiens
PTMD11538Q96MP815488
KCTD7
BTB/POZ domain-containing protein KCTD7
Homo sapiens
PTMD11851Q996157266
DNAJC7
DnaJ homolog subfamily C member 7
Homo sapiens
PTMD12004Q9BRB39091
PIGQ
Phosphatidylinositol N-acetylglucosaminyltransferase subunit Q
Homo sapiens
PTMD12717Q9H2X957468
SLC12A5
Solute carrier family 12 member 5
Homo sapiens
PTMD13693Q9NY466328
SCN3A
Sodium channel protein type 3 subunit alpha
Homo sapiens
PTMD14029Q9UBT651426
POLK
DNA polymerase kappa
Homo sapiens
PTMD14357Q9UL51610
HCN2
Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2
Homo sapiens
PTMD00926Q6222723957
Nr0b2
Nuclear receptor subfamily 0 group B member 2
Mus musculus