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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Camk2a-cre)159Kln
transgene insertion 159, Rudiger Klein
MGI:2176753
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Efnb2tm4Kln/Efnb2tm4Kln
Tg(Camk2a-cre)159Kln/0
involves: 129P2/OlaHsd * C57BL/6 MGI:3026783
cn2
Crhr1tm2Wrst/Crhr1tm2Wrst
Tg(Camk2a-cre)159Kln/0
involves: 129S2/SvPas * C57BL/6 MGI:2678102
cn3
Ntrk2tm2Kln/Ntrk2tm2Kln
Tg(Camk2a-cre)159Kln/?
involves: 129S2/SvPas * CBA/J MGI:3806579
cn4
Ntrk2tm1Bbd/Ntrk2tm2Kln
Tg(Camk2a-cre)159Kln/0
involves: 129S2/SvPas * CBA/J MGI:2448690
cn5
Bdnftm3Jae/Bdnftm3Jae
Tg(Camk2a-cre)159Kln/0
involves: 129S4/SvJae * CBA/J MGI:2176755
cn6
Hap1tm2Xjl/Hap1tm2Xjl
Tg(Camk2a-cre)159Kln/0
involves: 129S6/SvEvTac * BALB/c * C57BL/6 MGI:5695752
cn7
Gdf1tm1Dmus/Gdf1tm1Dmus
Tg(Camk2a-cre)159Kln/0
involves: 129X1/SvJ * C57BL/6 * CBA/J * SJL MGI:3806586


Genotype
MGI:3026783
cn1
Allelic
Composition
Efnb2tm4Kln/Efnb2tm4Kln
Tg(Camk2a-cre)159Kln/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Efnb2tm4Kln mutation (0 available); any Efnb2 mutation (28 available)
Tg(Camk2a-cre)159Kln mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mice showed no overt behavioral abnormalities

nervous system
N
• normal hippocampal architecture
• reduced early LTP but no significant defects of basal synaptic transmission parameters or NMDA receptor component




Genotype
MGI:2678102
cn2
Allelic
Composition
Crhr1tm2Wrst/Crhr1tm2Wrst
Tg(Camk2a-cre)159Kln/0
Genetic
Background
involves: 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Crhr1tm2Wrst mutation (0 available); any Crhr1 mutation (26 available)
Tg(Camk2a-cre)159Kln mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• in the light-dark box paradigm, mutant mice spend significantly more time in the lit compartment, display a decresead latency to enter the lit compartment, and show a signicantly higher number of entries into the lit compartment than control mice; however, no significant differences in the number of entries into the dark compartment are observed
• in the elevated plus maze test, mutant mice display significantly fewer head-dips in the protected arms as a percentage of total head dips, and an increase in the percentage of entries into the open arms; however, no significant differences in the number of entries into the closed arms are observed
• mutant mice display increased locomotor activity in the open-field paradigm

homeostasis/metabolism
• although basal plasma corticosterone levels are normal, mutant mice display significantly higher plasma corticosterone levels at 30 and 90 min after a 5-min restraint stress relative to similarly-stressed control mice
• although basal plasma ACTH levels are normal, mutant mice display significantly higher plasma ACTH levels at 30 and 90 min after a 5-min restraint stress relative to similarly-stressed control mice




Genotype
MGI:3806579
cn3
Allelic
Composition
Ntrk2tm2Kln/Ntrk2tm2Kln
Tg(Camk2a-cre)159Kln/?
Genetic
Background
involves: 129S2/SvPas * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ntrk2tm2Kln mutation (0 available); any Ntrk2 mutation (66 available)
Tg(Camk2a-cre)159Kln mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• basal synaptic transmission is normal but synaptic strengthening is impaired as evidenced by abnormal long term potentiation
• there is a reduced induction rate of LTP in hippocampal slices
• induction (measured as a signal 20% above baseline) only occurs 37.0% of the time after burst stimulation compared to 70% in controls
• similar results are observed after tetanus application
• impairment also occurs after long-lasting LTP (L-LTP) that is tested by repeated theta burst
• L-LTP induction rate is 14.2% compared to 62.5% and does not improve with increased stimulus strength




Genotype
MGI:2448690
cn4
Allelic
Composition
Ntrk2tm1Bbd/Ntrk2tm2Kln
Tg(Camk2a-cre)159Kln/0
Genetic
Background
involves: 129S2/SvPas * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ntrk2tm1Bbd mutation (2 available); any Ntrk2 mutation (66 available)
Ntrk2tm2Kln mutation (0 available); any Ntrk2 mutation (66 available)
Tg(Camk2a-cre)159Kln mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• a certain degree of task-specific long-term memory appears to be present but mutants show increasingly impaired learning behavior or inappropriate coping response when facing complex and/or stressful learning paradigms such as in contextual fear conditioning, two-way avoidance, radial maze and water maze learning
• in avoidance learning, mutants first react normally to the new environment but fall into a persisting maladaptive locomotor activity
• in the contextual fear conditioning, mutants fail to develop an appropriate freezing response after 30 min but show correct freezing after 24 hours yet not following exposure to tone
• mutants show impaired spatial learning in the Morris water maze test and partial impairment in the eight-arm radial maze
• mutants exhibit persistent thigmotaxis in the water maze

nervous system
• the number of myelinated axons in the CA1 region of the hippocampus is reduced by 23%
• reduction in LTP at CA1 hippocampal synapses




Genotype
MGI:2176755
cn5
Allelic
Composition
Bdnftm3Jae/Bdnftm3Jae
Tg(Camk2a-cre)159Kln/0
Genetic
Background
involves: 129S4/SvJae * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bdnftm3Jae mutation (2 available); any Bdnf mutation (41 available)
Tg(Camk2a-cre)159Kln mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological

growth/size/body




Genotype
MGI:5695752
cn6
Allelic
Composition
Hap1tm2Xjl/Hap1tm2Xjl
Tg(Camk2a-cre)159Kln/0
Genetic
Background
involves: 129S6/SvEvTac * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hap1tm2Xjl mutation (0 available); any Hap1 mutation (37 available)
Tg(Camk2a-cre)159Kln mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• 2 month old mice show increased immobility in the forced swim test and in the tail suspension test
• mice treated with imipramine, a tricyclic antidepressant, show increased mobility in the forced swim test and the tail suspension test
• mice exhibit lower preference to 1% sucrose solution than controls, indicating anhedonia
• mice perform better on the rotarod most likely due to smaller body size

cellular
• a decrease in proliferating cells is seen in the hippocampal dentate gyrus, indicating a decrease in postnatal neurogenesis

growth/size/body
• mild decrease in body weight during postnatal life, however by 4 months of age, weight is similar to controls

nervous system
• a decrease in proliferating cells is seen in the hippocampal dentate gyrus, indicating a decrease in postnatal neurogenesis

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
melancholic depression DOID:1595 OMIM:608516
J:224698




Genotype
MGI:3806586
cn7
Allelic
Composition
Gdf1tm1Dmus/Gdf1tm1Dmus
Tg(Camk2a-cre)159Kln/0
Genetic
Background
involves: 129X1/SvJ * C57BL/6 * CBA/J * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gdf1tm1Dmus mutation (1 available); any Gdf1 mutation (8 available)
Tg(Camk2a-cre)159Kln mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mice exhibit normal behavior

nervous system
N
• the hippocampus and neurons within the hippocampus are normal





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory