abnormal seizure response to electrical stimulation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the seizure activity response that is brought about by high or low frequency electrical stimulation (Mammalian Phenotype Ontology, MP_0001650)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001650
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Genes

22 gene mutations causing the abnormal seizure response to electrical stimulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AKT3 v-akt murine thymoma viral oncogene homolog 3
AP3M2 adaptor-related protein complex 3, mu 2 subunit
APOE apolipoprotein E
CELF4 CUGBP, Elav-like family member 4
CREM cAMP responsive element modulator
DNM1 dynamin 1
FCGR2B Fc fragment of IgG, low affinity IIb, receptor (CD32)
FOSB FBJ murine osteosarcoma viral oncogene homolog B
GFRA2 GDNF family receptor alpha 2
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A
HEXB hexosaminidase B (beta polypeptide)
HRH2 histamine receptor H2
HTR7 5-hydroxytryptamine (serotonin) receptor 7, adenylate cyclase-coupled
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3
PRICKLE1 prickle homolog 1 (Drosophila)
PRICKLE2 prickle homolog 2 (Drosophila)
SCN1A sodium channel, voltage gated, type I alpha subunit
SCN9A sodium channel, voltage gated, type IX alpha subunit
SLC1A3 solute carrier family 1 (glial high affinity glutamate transporter), member 3
SYN1 synapsin I
SZT2 seizure threshold 2 homolog (mouse)