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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Kalrntm1Ppen
targeted mutation 1, Peter Penzes
MGI:4358076
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Kalrntm1Ppen/Kalrntm1Ppen Not Specified MGI:4358084
ht2
Kalrntm1Ppen/Kalrn+ Not Specified MGI:4358085


Genotype
MGI:4358084
hm1
Allelic
Composition
Kalrntm1Ppen/Kalrntm1Ppen
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kalrntm1Ppen mutation (0 available); any Kalrn mutation (170 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Brain region specific and age-dependent alterations in spine density in Kalrntm1Ppen/Kalrntm1Ppen mice

nervous system
• at 12 weeks, neurons exhibit age-dependent reduction in spine density unlike wild-type neurons
• mature cortical pyramidal neurons exhibit lower spine density than in wild-type neurons
• however, spine density is rescued by over-expression of Kalrn
• AMPAR-mediated synaptic transmission is reduced in layer V pyramidal neurons from acute frontal cortical slices compared with wild-type slices
• AMPAR miniature excitatory postsynaptic currents (mEPSCs) frequency is reduced compared to in wild-type mice
• however, AMPAR mESPC amplitudes are normal
• AMPAR miniature excitatory postsynaptic currents (mEPSCs) frequency is reduced compared to in wild-type mice
• however, AMPAR mESPC amplitudes are normal

behavior/neurological
• mice fail to exhibit improved performance between the first and second trial in a Morris water maze unlike wild-type mice
• however, spatial reference memory and working memory at 3 weeks are normal
• at 12 weeks, mice exhibit impaired working memory performance in a Y-maze compared to wild-type mice
• at 12 weeks, mice exhibit increased spontaneous motor activity in an automated cage and in the Y-maze with intramaze cues compared with wild-type mice
• however, locomotor activity at 3 weeks is normal
• mice spend less time on the social side and more time on the non-social side of a 3-chamber social behavior apparatus than wild-type mice

homeostasis/metabolism
• neurons fail to exhibit an increase in spine area 30-minutes post-APV treatment unlike similarly treated wild-type cells




Genotype
MGI:4358085
ht2
Allelic
Composition
Kalrntm1Ppen/Kalrn+
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kalrntm1Ppen mutation (0 available); any Kalrn mutation (170 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice exhibit an intermediate increase in locomotor activity compared to wild-type mice that is reversed by treatment with clozapine





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
05/07/2024
MGI 6.23
The Jackson Laboratory