Phenotypes Associated with This Genotype

Genotype
MGI:5523888

• Allelic Composition: Scn1a^tm2.1Kzy/Scn1a⁺; Tg(Pvalb-cre)1Tama/0
• Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * DBA

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

behavior/neurological

convulsive seizures ( J:202863 )

• some mice develop recurrent seizures after P16

mortality/aging

postnatal lethality ( J:202863 )

• some mice develop recurrent seizures after P16 and experience sporadic sudden death

nervous system

convulsive seizures ( J:202863 )

• some mice develop recurrent seizures after P16

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
Dravet syndrome		DOID:0080422	OMIM:607208	J:202863