clonic seizures Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	increased number or decreased threshold for the induction of a seizure characterized by unilateral or bilateral rhythmic jerking movements of the arms and legs caused by alternating contraction and relaxation of muscle (Mammalian Phenotype Ontology, MP_0003996)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003996
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Genes

13 gene mutations causing the clonic seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
ARX	aristaless related homeobox
BSN	bassoon presynaptic cytomatrix protein
CACNA1A	calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CACNB4	calcium channel, voltage-dependent, beta 4 subunit
CHRNA4	cholinergic receptor, nicotinic, alpha 4 (neuronal)
GABBR1	gamma-aminobutyric acid (GABA) B receptor, 1
GABBR2	gamma-aminobutyric acid (GABA) B receptor, 2
LGI1	leucine-rich, glioma inactivated 1
MYO5A	myosin VA (heavy chain 12, myoxin)
PCMT1	protein-L-isoaspartate (D-aspartate) O-methyltransferase
SCN1A	sodium channel, voltage gated, type I alpha subunit
SLC13A1	solute carrier family 13 (sodium/sulfate symporter), member 1
SPTBN2	spectrin, beta, non-erythrocytic 2