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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Adktm2Bois
targeted mutation 2, Detlev Boison
MGI:5816711
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Adktm2Bois/Adktm2Bois
Adora1tm1Bbf/Adora1tm1Bbf
Tg(Nes-cre)1Kln/0
involves: 129P2/OlaHsd * C57BL/6 * SJL MGI:5816716
cn2
Adktm2Bois/Adktm2Bois
Adora2atm1Jfc/Adora2atm1Jfc
Tg(Nes-cre)1Kln/0
involves: 129S4/SvJae * C57BL/6 * SJL MGI:5816717
cn3
Adktm2Bois/Adktm2Bois
Tg(Nes-cre)1Kln/0
involves: C57BL/6 * SJL MGI:5816712


Genotype
MGI:5816716
cn1
Allelic
Composition
Adktm2Bois/Adktm2Bois
Adora1tm1Bbf/Adora1tm1Bbf
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Adktm2Bois mutation (0 available); any Adk mutation (51 available)
Adora1tm1Bbf mutation (1 available); any Adora1 mutation (23 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice exhibit increased susceptibility to stress-induced (placement in novel environment) seizures

mortality/aging
• increase in mortality

nervous system
• mice exhibit increased susceptibility to stress-induced (placement in novel environment) seizures




Genotype
MGI:5816717
cn2
Allelic
Composition
Adktm2Bois/Adktm2Bois
Adora2atm1Jfc/Adora2atm1Jfc
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Adktm2Bois mutation (0 available); any Adk mutation (51 available)
Adora2atm1Jfc mutation (2 available); any Adora2a mutation (40 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• mice exhibit a resistance to stress-induced (placement in novel environment) seizures

behavior/neurological
N
• mice exhibit normal associative learning and contextual learning
• mice exhibit a resistance to stress-induced (placement in novel environment) seizures




Genotype
MGI:5816712
cn3
Allelic
Composition
Adktm2Bois/Adktm2Bois
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Adktm2Bois mutation (0 available); any Adk mutation (51 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice show increased susceptibility to induced seizures with the adenosine A1 receptor antagonist DPCPX, and a single high dose of DPCPX consistently triggers lethal status epilepticus in mutants but not controls
• pretreatment with antagonists to adenosine A2a receptor (SCH58261) and TrkB (Ana-12) significantly extend the survival time after DPCPX-induced seizures
• associative learning in the conditioned freezing paradigm is decreased during conditioned stimulus 2
• however, the percentage time freezing during conditioned stimulus 3 and 4 is increased compared with baseline conditioned stimulus 1 freezing indicating that mice show a general ability to learn
• mice show a deficit in contextual memory with freezing rates comparable to baseline
• however, mutants show no differences from controls in the elevated plus maze, acoustic startle response, or spatial working memory and the response to foot shock is normal
• from 2 months of age, mice exhibit increased susceptibility to stress-induced seizures (placement in novel environment) which are characterized by tonic-clonic convulsions
• by 3 months of age, 44% of mutants react with a seizure when placed into a novel environment, by 4 months, seizure incidence is 89% and by 6 months, 100%
• the probability of an evoked seizure response rises from 7.4% at 2 months to 77% at 6 months
• EEG recordings indicate spontaneous seizures with average seizure rate of 0.85 seizures per day and average duration of 43.6 +/- 7.4 seconds

nervous system
• mice show increased susceptibility to induced seizures with the adenosine A1 receptor antagonist DPCPX, and a single high dose of DPCPX consistently triggers lethal status epilepticus in mutants but not controls
• pretreatment with antagonists to adenosine A2a receptor (SCH58261) and TrkB (Ana-12) significantly extend the survival time after DPCPX-induced seizures
• from 2 months of age, mice exhibit increased susceptibility to stress-induced seizures (placement in novel environment) which are characterized by tonic-clonic convulsions
• by 3 months of age, 44% of mutants react with a seizure when placed into a novel environment, by 4 months, seizure incidence is 89% and by 6 months, 100%
• the probability of an evoked seizure response rises from 7.4% at 2 months to 77% at 6 months
• EEG recordings indicate spontaneous seizures with average seizure rate of 0.85 seizures per day and average duration of 43.6 +/- 7.4 seconds
• mice have increased adenosine A2a receptor-mediated synaptic plasticity
• mice have increased levels of synaptic adenosine
• treatment of hippocampal slices from epileptic mutants with the adenosine A1 receptor antagonist DPCPX results in a higher disinhibition of synaptic transmission than controls
• maximum fEPSP slope is higher in mutant hippocampal slices than in controls
• hippocampal slices show an increase in theta-burst-induced LTP magnitude
• treatment with the adenosine A2a receptor-selective antagonist SCH58261resverses the LTP magnitude
• treatment with the tyrosine kinase inhibitor K25a abolishes the increased LTP magnitude





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory