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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Scn2btm1Isom
targeted mutation 1, Lori L Isom
MGI:2451362
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Scn2btm1Isom/Scn2btm1Isom involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:2451363


Genotype
MGI:2451363
hm1
Allelic
Composition
Scn2btm1Isom/Scn2btm1Isom
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scn2btm1Isom mutation (0 available); any Scn2b mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• susceptibility to pharmacologically induced seizures
• although nervous system function is generally normal, homozygotes are prone to epileptic seizures induced by pilocarpine
• time to reach stage 3 seizures is significantly reduced
• succeptibility is greater after 10 generations of backcrossing to C57BL/6J as compared to the F2 generation

nervous system
• susceptibility to pharmacologically induced seizures
• although nervous system function is generally normal, homozygotes are prone to epileptic seizures induced by pilocarpine
• time to reach stage 3 seizures is significantly reduced
• succeptibility is greater after 10 generations of backcrossing to C57BL/6J as compared to the F2 generation
• reduced maximal amplitude of sodium current in isolated hippocampal neurons
• is also a reduced negative shift in the voltage dependence of inactivation
• 30-40% reduction in the sodium current in the optic nerve
• no changes in conductance velocity





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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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory