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Phenotypes Associated with This Genotype
Genotype
MGI:3713740
Allelic
Composition
Scn1atm1Kzy/Scn1a+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scn1atm1Kzy mutation (0 available); any Scn1a mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• spontaneous death occurs at 25% and 40% within the first and third postnatal months, respectively

behavior/neurological
• beginning at P3 and exhibiting recurrent spontaneous seizures after P18
• however, genetic background percentage has little effect on seizure occurrences

nervous system
• beginning at P3 and exhibiting recurrent spontaneous seizures after P18
• however, genetic background percentage has little effect on seizure occurrences

Mouse Models of Human Disease
OMIM ID Ref(s)
Epileptic Encephalopathy, Early Infantile, 6; EIEE6 607208 J:121969


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/26/2016
MGI 6.03
The Jackson Laboratory