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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Camk2atm1Sva
targeted mutation 1, Alcino Silva
MGI:1857279
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Camk2atm1Sva/Camk2atm1Sva involves: 129P2/OlaHsd MGI:3764505
hm2
Camk2atm1Sva/Camk2atm1Sva involves: 129P2/OlaHsd * BALB/c MGI:3764503
hm3
Camk2atm1Sva/Camk2atm1Sva involves: 129P2/OlaHsd * C57BL/6J MGI:3764506
ht4
Camk2atm1Sva/Camk2a+ B6.129P2-Camk2atm1Sva/J MGI:6189158
ht5
Camk2atm1Sva/Camk2a+ involves: 129P2/OlaHsd * C57BL/6J MGI:3764507


Genotype
MGI:3764505
hm1
Allelic
Composition
Camk2atm1Sva/Camk2atm1Sva
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Camk2atm1Sva mutation (1 available); any Camk2a mutation (136 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• short term potentiation is absent
• however, post-tetanic potentiation is normal
• mice exhibit little to no long term potentiation after a priming period of low-frequency stimulation unlike in wild-type mice
• long term depression is present but reduced compared to in wild-type mice




Genotype
MGI:3764503
hm2
Allelic
Composition
Camk2atm1Sva/Camk2atm1Sva
Genetic
Background
involves: 129P2/OlaHsd * BALB/c
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Camk2atm1Sva mutation (1 available); any Camk2a mutation (136 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• mice exhibit normal nervous system anatomy
• 14 of 16 mice display no long term potentiation

behavior/neurological
• mice appear more 'jumpy' than wild-type mice and frantically avoid human contact
• however, mice exhibit otherwise normal behavior




Genotype
MGI:3764506
hm3
Allelic
Composition
Camk2atm1Sva/Camk2atm1Sva
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Camk2atm1Sva mutation (1 available); any Camk2a mutation (136 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• 38.28+/-11.0 mm3 compared to 32.0+/-8.1 mm3 in heterozygotes and 18.8+/-5.1 mm3 in wild-type mice

homeostasis/metabolism
• 38.28+/-11.0 mm3 compared to 32.0+/-8.1 mm3 in heterozygotes and 18.8+/-5.1 mm3 in wild-type mice




Genotype
MGI:6189158
ht4
Allelic
Composition
Camk2atm1Sva/Camk2a+
Genetic
Background
B6.129P2-Camk2atm1Sva/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Camk2atm1Sva mutation (1 available); any Camk2a mutation (136 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• severe working memory deficits in the eight-arm radial maze task and delayed alternation task using modified T-maze
• however, performance in reference memory tasks are normal
• mice exhibit high levels of aggression towards cage mates, with more than half of cage mates killed by mutants by 3 years of age
• however, mice exhibit normal body temperature and normal behaviors in the wire hang test, grip strength test, rotarod test, hot plate test, acoustic startle response, and prepulse inhibition test
• depression-like behavior is decreased in the Porsolt forced swim test
• anxiety-like behavior is decreased both in the light/dark transition test and in the elevated plus maze test
• mice exhibit exaggerated infradian oscillatory locomotor activity, with 24 hour locomotor activity positively correlated with time spent in the center of the open field, negatively correlated with percentage of immobility time in the force swim test, and correlated with anxiety- and depression-like behaviors (J:234969)
• expression of many circadian genes correlates with infradian rhythm behavior (J:234969)
• infradian oscillatory locomotor activity responds to mood stabilizer treatment, with lamotrigine increasing home cage locomotor activity and carbamazepine decreasing home cage locomotor activity (J:234969)
• mice exhibit an exaggerated infradian rhythm (J:263327)
• pattern of locomotor activity changes over time, showing periodic mood-change-like behavior in the home cage, with one cycle of approximately 1-2 weeks (J:263327)
• mice show more variable activity patterns in the total distance traveled in the dark period in their home cages (J:263327)
• the locomotor activity pattern during a single day is different, with activity steadily increasing until morning compared to wild-type mice which have two peaks of activity during the dark phase (J:263327)
• mice show increased locomotor activity in the open field and in the social interaction test in a novel environment

growth/size/body

cellular
• BrdU-labeled cells are increased by 53% in the dentate gyrus, indicating increased proliferation in this region

nervous system
• mice exhibit increased number of immature neurons and decreased number of mature neurons in the dentate gyrus, decreased dendritic branching and length in the dentate gyrus, and neurons with electrophysiological features characteristic of immature neurons, indicating that the dentate gyrus is immature
• majority of dentate gyrus granule cells fail to develop into mature neurons
• the mossy fiber-CA3 synapses are poorly developed in the hippocampus
• formation of postsynaptic densities in the mossy fiber terminals is reduced
• formation of synaptic vesicles in the mossy fiber terminals is reduced
• dentate gyrus neurons exhibit functional abnormalities, including higher input resistance, slightly depolarized resting membrane potentials, high excitability, decreased number of spikes during sustained depolarization, and greatly reduced facilitation at mossy fiber-CA3 synapses
• mutants show abnormal transmission at the synapses between granule cell axons, mossy fibers, and the CA1 pyramidal cells, with increased basal transmission and decreased large facilitation
• increase in striatal dopamine turnover in the brain

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
bipolar disorder DOID:3312 J:234969




Genotype
MGI:3764507
ht5
Allelic
Composition
Camk2atm1Sva/Camk2a+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Camk2atm1Sva mutation (1 available); any Camk2a mutation (136 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• 32.0+/-8.1 mm3 compared to 38.28+/-11.0 mm3 in homozygotes and 18.8+/-5.1 mm3 in wild-type mice

homeostasis/metabolism
• 32.0+/-8.1 mm3 compared to 38.28+/-11.0 mm3 in homozygotes and 18.8+/-5.1 mm3 in wild-type mice





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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
04/23/2024
MGI 6.23
The Jackson Laboratory