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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Scttm1Inis
targeted mutation 1, Ichiko Nishijima
MGI:3815315
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Scttm1Inis/Scttm1Inis involves: 129S7/SvEvBrd * C57BL/6 MGI:3815317


Genotype
MGI:3815317
hm1
Allelic
Composition
Scttm1Inis/Scttm1Inis
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scttm1Inis mutation (0 available); any Sct mutation (11 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• despite defects in hippocampal physiology, there is no difference in the number of dendritic branches or in the morphology of spines on apical dendrites in pyramidal neurons in the CA1 region
• significant reduction in hippocampal long term potentiation immediately following high frequency stimulation and throughout the induction and maintenance phases
• reduction in post-tetanic potentiation
• significant deficit in paired pulse facilitation at both 20 ms and 40 ms inter-pulse intervals





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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
11/19/2024
MGI 6.24
The Jackson Laboratory