abnormal kindling response Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the long-lasting epileptogenic changes normally induced by daily sub threshold electrical brain stimulation, often used as an induced model for epilepsy (Mammalian Phenotype Ontology, MP_0001499)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001499
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Genes

9 gene mutations causing the abnormal kindling response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AP3M2 adaptor-related protein complex 3, mu 2 subunit
APOE apolipoprotein E
CREM cAMP responsive element modulator
DNM1 dynamin 1
GFRA2 GDNF family receptor alpha 2
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A
SCN9A sodium channel, voltage gated, type IX alpha subunit
SLC1A3 solute carrier family 1 (glial high affinity glutamate transporter), member 3
SZT2 seizure threshold 2 homolog (mouse)