All Phenotypes Scn8a<em1Mm> MGI Mouse

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Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

Scn8a^em1Mm
endonuclease-mediated mutation 1, Miriam Meisler
MGI:5578212

Summary

1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
ht1	Scn8a^em1Mm/Scn8a⁺	involves: C57BL/6J * SJL	MGI:5578216

Allelic Composition	Scn8a^em1Mm/Scn8a⁺
Genetic Background	involves: C57BL/6J * SJL

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scn8a^em1Mm mutation (0 available); any Scn8a mutation (99 available)

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

mortality/aging

premature death ( J:207931 )

• sudden unexpected death in epilepsy

behavior/neurological

abnormal behavior ( J:207931 )

seizures ( J:207931 )

• with sudden unexpected death in epilepsy

nervous system

seizures ( J:207931 )

• with sudden unexpected death in epilepsy

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
early infantile epileptic encephalopathy		DOID:0050709		J:207931

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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