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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Bdnftm1Par
targeted mutation 1, Luis Parada
MGI:1929986
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Bdnftm1Par/Bdnftm1Par involves: 129S1/Sv MGI:2175722
ht2
Bdnftm1Par/Bdnf+ B6.129S1-Bdnftm1Par MGI:3664866
ht3
Bdnftm1Par/Bdnf+ involves: 129S1/Sv MGI:3664865
cx4
Bdnftm1Par/Bdnf+
Ntrk2tm1.1Tes/Ntrk2tm1.1Tes
B6.129S1-Bdnftm1Par Ntrk2tm1.1Tes MGI:3833380
cx5
Bdnftm1Par/Bdnf+
Ntrk2tm1.1Tes/Ntrk2+
B6.129S1-Bdnftm1Par Ntrk2tm1.1Tes MGI:3833382
cx6
Bdnftm1Par/Bdnftm1Par
Ntf3tm1Par/Ntf3tm1Par
involves: 129S1/Sv MGI:3612887
cx7
Bdnftm1Par/Bdnftm1Par
Ntf5tm1Par/Ntf5tm1Par
involves: 129S1/Sv * C57BL/6 MGI:3613013


Genotype
MGI:2175722
hm1
Allelic
Composition
Bdnftm1Par/Bdnftm1Par
Genetic
Background
involves: 129S1/Sv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bdnftm1Par mutation (0 available); any Bdnf mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• die within 2 weeks of birth

nervous system
• increase in dorsal root ganglion neuron apoptosis
• delay in barrel formation through P6, but the deficiency disappears by P8
• innervation into layer IV of the cortex by thalamic axons is uniform (rather than segregated into individual barrels) at P6, but becomes less apparent by P8
• reduction of neurons in sensory ganglia, however motor neuron numbers are normal (J:44286)
• majority of sensory neuron loss occurs before E13.5 (J:44286)
• 50% reduction of neurons in the geniculate ganglion
• 39% reduction of neurons in the nodose/petrosal ganglion
• 21% reduction of neurons in the trigeminal ganglion (J:44286)
• 39% reduction of neurons in the nodose/petrosal ganglion
• dorsal root ganglion neuronal cultures exhibit about 50% reduction in numbers of Bdnf and Ntf5-responsive neurons, but not of Ntf3-responsive neruons
• 36% reduction of neurons in the L4 dorsal root ganglion
• 31% reduction of dorsal root ganglion neurons by E13

cellular
• increase in dorsal root ganglion neuron apoptosis




Genotype
MGI:3664866
ht2
Allelic
Composition
Bdnftm1Par/Bdnf+
Genetic
Background
B6.129S1-Bdnftm1Par
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bdnftm1Par mutation (0 available); any Bdnf mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• age-related increase in food intake beggining around 6 weeks of age
• by 4-7 months of age mice consume about 25% more food than wild-type littermates
• chronic fluoxetine treatment partially suppresses hyperphagia
• decrease in latency to attack an intruder and increase in number of biting attacks (J:59077)
• latency to attack progressively decreases over repeated trials (J:59077)
• treatment with fluoxetine reduced aggression to a level similar to that in wild-type mice (J:59077)
• male mice have decreased latency time to first biting attack against intruder males compared to wild-type controls (J:144845)
• male mice also have a significantly increased number of biting attacks over a 5 minute period (J:144845)
• increased time spent in the center area during a 10 minute period in and open field; however, overall locomotor activity in an open field is not different from wild-type
• during a 10 minute trial in an open field

growth/size/body
• mice gain weight with age with a mean 10 gram difference occurring by 6 months of age
• first detected at 2-4 months of age and by 12-18 months of age body weight is 34% higher than wild-type littermates

nervous system
• progressive loss of serotonin axons is seen in 12 to 18 month old mice
• abnormal induction of Fos by dexfenfluramine (reduced in the bed nucleus of the stria terminalis, the central nucleus of the amygdala, parts of the caudate-putamen, the shell region of the nucleus accumbens, and the thalamic nuclei; increased in the pyramidal neurons of the hippocampus) indicates abnormal neuronal activation induced by 5-HT release

homeostasis/metabolism
• about 2-fold higher at 12 months of age
• forebrain levels of 5-HT and 5-hydroxyindoleacetic acid (5-HIAA) are significantly lower in old but not in young mice
• at 18 months of age the ratio of 5-HIAA to 5-HT is lower in the hypothalamus




Genotype
MGI:3664865
ht3
Allelic
Composition
Bdnftm1Par/Bdnf+
Genetic
Background
involves: 129S1/Sv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bdnftm1Par mutation (0 available); any Bdnf mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• decreased exploratory behavior as measured by percentage of time spent in the center and number of entries into the center of and open field over a 2 hour period; however no significant change in total locomotor activity is detected
• increase in intermale aggression
• decrease in time spent in the open arms and numbers of entries into the open arms in an elevated plus maze

nervous system
• 13.8 +/- 0.6% reduction in hippocampal volume

growth/size/body
• first detected at 2 months of age




Genotype
MGI:3833380
cx4
Allelic
Composition
Bdnftm1Par/Bdnf+
Ntrk2tm1.1Tes/Ntrk2tm1.1Tes
Genetic
Background
B6.129S1-Bdnftm1Par Ntrk2tm1.1Tes
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bdnftm1Par mutation (0 available); any Bdnf mutation (42 available)
Ntrk2tm1.1Tes mutation (0 available); any Ntrk2 mutation (66 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• male mice have decreased latency time to first biting attack against intruder males compared to wild-type controls
• male mice also have a significantly increased number of biting attacks over a 5 minute period
• the latency time and number of attacks are not to the same degree as mice that only carry the Bdnftm1Par mutant allele

growth/size/body
• mice gain weight with age though not to the degree as mice that only carry the Bdnftm1Par mutant allele




Genotype
MGI:3833382
cx5
Allelic
Composition
Bdnftm1Par/Bdnf+
Ntrk2tm1.1Tes/Ntrk2+
Genetic
Background
B6.129S1-Bdnftm1Par Ntrk2tm1.1Tes
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bdnftm1Par mutation (0 available); any Bdnf mutation (42 available)
Ntrk2tm1.1Tes mutation (0 available); any Ntrk2 mutation (66 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• male mice have decreased latency time to first biting attack against intruder males compared to wild-type controls
• male mice also have a significantly increased number of biting attacks over a 5 minute period
• the latency time and number of attacks are not to the same degree as mice that only carry the Bdnftm1Par mutant allele




Genotype
MGI:3612887
cx6
Allelic
Composition
Bdnftm1Par/Bdnftm1Par
Ntf3tm1Par/Ntf3tm1Par
Genetic
Background
involves: 129S1/Sv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bdnftm1Par mutation (0 available); any Bdnf mutation (42 available)
Ntf3tm1Par mutation (0 available); any Ntf3 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• die within the first day of birth

nervous system
• 100% reduction of neurons in the spiral ganglia
• reduction of neurons in sensory ganglia, however motor neuron numbers are normal
• sensory neuron loss occurs from E12.5 to P0.5
• 65% reduction of neurons in the geniculate ganglion
• 62% reduction of neurons in the nodose/petrosal ganglion
• 74% reduction of neurons in the trigeminal ganglion
• 62% reduction of neurons in the nodose/petrosal ganglion
• 100% reduction of neurons in the vestibular ganglia
• 83% reduction of neurons in the L4 dorsal root ganglion




Genotype
MGI:3613013
cx7
Allelic
Composition
Bdnftm1Par/Bdnftm1Par
Ntf5tm1Par/Ntf5tm1Par
Genetic
Background
involves: 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bdnftm1Par mutation (0 available); any Bdnf mutation (42 available)
Ntf5tm1Par mutation (0 available); any Ntf5 mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• reduction in number of differentiated dorsal root ganglion neurons at E13, indicating delayed neuronal differentiation, however numbers of sensory neurons are normal
• dorsal root ganglion neuronal cultures exhibit reduced numbers of Bdnf and Ntf5-responsive neurons and increased numbers of Ntf3-dependent neurons

cellular
• reduction in number of differentiated dorsal root ganglion neurons at E13, indicating delayed neuronal differentiation, however numbers of sensory neurons are normal





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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory