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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cpne6tm1.1Rueg
targeted mutation 1.1, Markus Ruegg
MGI:5882517
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cpne6tm1.1Rueg/Cpne6tm1.1Rueg B6.Cg-Cpne6tm1.1Rueg MGI:6279162
hm2
Cpne6tm1.1Rueg/Cpne6tm1.1Rueg involves: 129 * 129S1/Sv * C57BL/6 MGI:6279160


Genotype
MGI:6279162
hm1
Allelic
Composition
Cpne6tm1.1Rueg/Cpne6tm1.1Rueg
Genetic
Background
B6.Cg-Cpne6tm1.1Rueg
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cpne6tm1.1Rueg mutation (0 available); any Cpne6 mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• adult male homozygotes exhibit normal open field behavior and foot-shock sensitivity
• in a fear-conditioning paradigm, adult male homozygotes exhibit a significant deficit in learning and context-dependent memory relative to wild-type controls
• however, no deficits are observed in amygdala-dependent cued memory




Genotype
MGI:6279160
hm2
Allelic
Composition
Cpne6tm1.1Rueg/Cpne6tm1.1Rueg
Genetic
Background
involves: 129 * 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cpne6tm1.1Rueg mutation (0 available); any Cpne6 mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• adult homozygotes exhibit normal levels of postsynaptic density proteins and calcium signaling targets and normal brain weight and morphology, with no significant changes in spine density and morphology or frequency and amplitude of miniature excitatory and inhibitory postsynaptic currents in hippocampal CA1 neurons relative to wild-type controls
• after 40 min of chemical LTP induction, DIV21 (day in vitro 21) cultured hippocampal neurons fail to exhibit a significant increase in postsynaptic spine head width, unlike wild-type hippocampal neurons
• after 40 min of chemical LTP induction, DIV21 cultured hippocampal neurons fail to exhibit a significant increase in postsynaptic spine head width, indicating absence of spine structural plasticity
• after high-frequency stimulation of Schaffer collaterals, the initial increase in excitatory postsynaptic current in CA1 pyramidal neurons is normal but the fEPSP slope returns to baseline within 60 min of LTP induction, unlike in wild-type controls
• however, the input-output ratio of Schaffer collateral-CA1 connections and paired-pulse ratio (fEPSP2 slope to fEPSP1 slope) are normal
• adult homozygotes show a deficit in hippocampal LTP maintenance, as measured by fEPSPs in CA1 pyramidal neurons by high-frequency stimulation of Schaffer collaterals in acute hippocampal slices
• short-term treatment of acute hippocampal slices with jasplakinolid (an actin stabilizer) fully restores the LTP deficit in CA1 neurons to wild-type levels
• NMDA receptor-dependent long term depression (LTD), triggered by low-frequency stimulation at 1Hz, is normal





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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
12/10/2024
MGI 6.24
The Jackson Laboratory