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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ntrk2tm2Kln
targeted mutation 2, Rudiger Klein
MGI:1933974
Summary 8 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ntrk2tm2Kln/Ntrk2tm2Kln involves: 129S2/SvPas MGI:2175189
cn2
Ntrk2tm2Kln/Ntrk2tm2Kln
Tg(Penk-cre,-lacZ)1Mini/0
involves: 129S2/SvPas MGI:5532658
cn3
Ntrk2tm2Kln/Ntrk2tm2Kln
Slc1a3tm1(cre/ERT2)Mgoe/?
Gt(ROSA)26Sortm1Sor/?
involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6 * SJL MGI:3830091
cn4
Ntrk2tm2Kln/Ntrk2tm2Kln
Tg(Cck-cre,-lacZ)1Mini/0
involves: 129S2/SvPas * C57BL/6 * CBA MGI:5575864
cn5
Ntrk2tm2Kln/Ntrk2tm2Kln
Tg(Nes-cre)1Kln/0
involves: 129S2/SvPas * C57BL/6 * SJL MGI:4840349
cn6
Ntrk2tm1Bbd/Ntrk2tm2Kln
Tg(Camk2a-cre)159Kln/0
involves: 129S2/SvPas * CBA/J MGI:2448690
cn7
Ntrk2tm2Kln/Ntrk2tm2Kln
Tg(Camk2a-cre)159Kln/?
involves: 129S2/SvPas * CBA/J MGI:3806579
cn8
Ntrk2tm2Kln/Ntrk2tm2Kln
Slc1a3tm1(cre/ERT2)Mgoe/?
Tg(CAG-Bgeo/GFP)21Lbe/?
involves: 129/Sv * C57BL/6 * SJL MGI:3830092


Genotype
MGI:2175189
hm1
Allelic
Composition
Ntrk2tm2Kln/Ntrk2tm2Kln
Genetic
Background
involves: 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ntrk2tm2Kln mutation (0 available); any Ntrk2 mutation (66 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype




Genotype
MGI:5532658
cn2
Allelic
Composition
Ntrk2tm2Kln/Ntrk2tm2Kln
Tg(Penk-cre,-lacZ)1Mini/0
Genetic
Background
involves: 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ntrk2tm2Kln mutation (0 available); any Ntrk2 mutation (66 available)
Tg(Penk-cre,-lacZ)1Mini mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• from 2-14 months of age, mutants and controls show similar motor coordination and motor function (no differences in hind-paw clasping or rotarod performance)
• no differences in mutants and controls are detected with the inverted screen test
• young adult (3 month-old) mutants show significant increases in distance traveled in open field tests when acutely challenged with cocaine, compared to wild-type mice
• mutants display subtle gait differences compared to controls at 5 months, including a smaller print width for the left hind paw and differences in footfalls of 2 different paws and slight altered timely coordination between ipsilateral (right fore- and hind-) paws and girdle (right and left) hindpaws
• by 9 months of age and after, mutants show significantly higher locomotion in open field tests compared to wild-type
• observed when acutely challenged with cocaine at 3 months of age

nervous system
N
• no loss of medium-sized spiny neurons (MSNs) in the striatum is detected compared to wild-type littermates; striatal volume in normal at 12 months of age
• corticostriatal synaptic properties and striatopallidal projections are intact in mutants




Genotype
MGI:3830091
cn3
Allelic
Composition
Ntrk2tm2Kln/Ntrk2tm2Kln
Slc1a3tm1(cre/ERT2)Mgoe/?
Gt(ROSA)26Sortm1Sor/?
Genetic
Background
involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1Sor mutation (7 available); any Gt(ROSA)26Sor mutation (993 available)
Ntrk2tm2Kln mutation (0 available); any Ntrk2 mutation (66 available)
Slc1a3tm1(cre/ERT2)Mgoe mutation (0 available); any Slc1a3 mutation (70 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• fewer neurons arising in hippocampus from radial glial cells after treatment with tamoxifen survive to become mature neurons
• axon elongation is unaffected
• dendritic branching and lengths are reduced in neurons arising in the hippocampus from radial glial cells after treatment with tamoxifen
• reduced dendritic complexity 90 um from soma
• spine density is significantly reduced
• lasts only 30-40 minutes as compared to over 90 minutes for controls

behavior/neurological
• studied between 28 and 42 days after tamoxifen treatment
• enter the center in an open field test less frequently and spend less time there
• more time spent on the periphery in an open field test
• in an elevated + maze, fewer entries into the open arms and less time spent in the open arms
• studied between 28 and 42 days after tamoxifen treatment
• less spontaneous activity in an open field test

cellular
• fewer neurons arising in hippocampus from radial glial cells after treatment with tamoxifen survive to become mature neurons
• axon elongation is unaffected




Genotype
MGI:5575864
cn4
Allelic
Composition
Ntrk2tm2Kln/Ntrk2tm2Kln
Tg(Cck-cre,-lacZ)1Mini/0
Genetic
Background
involves: 129S2/SvPas * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ntrk2tm2Kln mutation (0 available); any Ntrk2 mutation (66 available)
Tg(Cck-cre,-lacZ)1Mini mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• mutants show greater weight gain in the first week on a high fat diet compared to controls on the same diet
• treatment with mifepristone stabilizes mutant body weight
• mutants gain more weight than controls on the same diet, despite no increase in food intake
• males develop obesity around 4 months of age, while females exhibit this around 5 months
• gonadal white adipose tissue fat pads are significantly increased in males and females

endocrine/exocrine glands
• from 3 months of age, thickness is increased becoming highly significant at 5 months, compared to controls
• beginning at 3 months, hypertrophy is observed, becoming significant by 5 months

adipose tissue
N
• interscapular brown adipose tissue are found in mutants and controls
• fat mass is significantly increased in 3 month-old and 9 month-old male mutants; however, fat-free mass is unaltered
• mutants have increased fat accumulation in the head/neck region
• gonadal white adipose tissue fat pads are significantly increased in males and females
• mesenteric adipose tissue fat pads are significantly increased in males and females

behavior/neurological
N
• no alterations in circadian rhythm or cumulative food intake at 2 or 8 months of age
• on a high fat diet, mutants exhibit decreased food intake similarly to controls
• open field activity and elevated plus maze behavior (indicator of anxiety-like behavior) does not differ between mutants and controls at any age
• home cage activity is significantly increased during the dark phase in 8 month-old obese mutants

nervous system
• GABAergic output of Cck interneurons onto Crh neurons is reduced; increased neuronal activity results

homeostasis/metabolism
N
• oxygen consumption and carbon dioxide production rates, as well as respiratory exchange ratio and energy expenditure are similar
• signicantly elevated in older obese mice
• signicantly elevated in older obese mice
• observed in older obese mice
• mutants show increased de novo lipogenesis in the liver
• afternoon levels are increased compared to controls

liver/biliary system
• gonadal white adipose tissue fat pads are significantly increased in males and females
• aged mice (5 months) show increased hepatic lipid stores compared to controls




Genotype
MGI:4840349
cn5
Allelic
Composition
Ntrk2tm2Kln/Ntrk2tm2Kln
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129S2/SvPas * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ntrk2tm2Kln mutation (0 available); any Ntrk2 mutation (66 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die between 3 and 8 months

nervous system
• expression of parvalbumin in the entorhinal cortex and the hippocampus is reduced compared to in wild-type mice
• in the most superficial layers of the neocortex dendrites are fasiculated and poorly stained while in the deepest layers (V-VI) staining is reduced compared to in wild-type mice
• in the most superficial layers of the neocortex dendrites are fasiculated and poorly stained while in the deepest layers (V-VI) staining is reduced compared to in wild-type mice
• delayed at E18.5
• mice exhibit severe caudal retraction of the cortical hemisphere compared to in wild-type mice
• however, the olfactory bulb and cerebellum are normal
• at E18.5, proliferating cells are more diffusely disturbed in the central part of the cortical plate compared to in wild-type mice
• the thickness of all layers is reduced compared to in wild-type mice
• layer II/III is slightly compressed with tightly packed neurons compared to in wild-type mice
• however, lamination is normal
• severely compressed
• in the central nervous system

behavior/neurological

growth/size/body

cellular
• expression of parvalbumin in the entorhinal cortex and the hippocampus is reduced compared to in wild-type mice
• in the most superficial layers of the neocortex dendrites are fasiculated and poorly stained while in the deepest layers (V-VI) staining is reduced compared to in wild-type mice
• in the most superficial layers of the neocortex dendrites are fasiculated and poorly stained while in the deepest layers (V-VI) staining is reduced compared to in wild-type mice
• delayed at E18.5




Genotype
MGI:2448690
cn6
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:3806579
cn7
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:3830092
cn8
Allelic
Composition
Ntrk2tm2Kln/Ntrk2tm2Kln
Slc1a3tm1(cre/ERT2)Mgoe/?
Tg(CAG-Bgeo/GFP)21Lbe/?
Genetic
Background
involves: 129/Sv * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ntrk2tm2Kln mutation (0 available); any Ntrk2 mutation (66 available)
Slc1a3tm1(cre/ERT2)Mgoe mutation (0 available); any Slc1a3 mutation (70 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• synaptic contacts appear to be normal for neurons arising in hippocampus from radial glial cells after treatment with tamoxifen





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory