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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(CAG-Tfb1m)AGsha
transgene insertion A, Gerald Shadel
MGI:5313807
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Prkaa2tm1Vio/Prkaa2+
Tg(CAG-Tfb1m)AGsha/0
involves: 129S2/SvPas * C57BL/6J * SJL/J MGI:5789745
cx2
E2f1tm1Meg/E2f1+
Tg(CAG-Tfb1m)AGsha/0
involves: 129S4/SvJae * C57BL/6J * SJL/J MGI:5488619
tg3
Tg(CAG-Tfb1m)AGsha/0 B6J.Cg-Tg(CAG-Tfb1m)AGsha MGI:5789744
tg4
Tg(CAG-Tfb1m)AGsha/? involves: C57BL/6J * SJL/J MGI:5488618


Genotype
MGI:5789745
cx1
Allelic
Composition
Prkaa2tm1Vio/Prkaa2+
Tg(CAG-Tfb1m)AGsha/0
Genetic
Background
involves: 129S2/SvPas * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prkaa2tm1Vio mutation (1 available); any Prkaa2 mutation (35 available)
Tg(CAG-Tfb1m)AGsha mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
N
• ABR thresholds are similar to wild-type controls, indicating rescue or delay of the premature hearing loss seen in single Tg(CAG-Tfb1m)AGsha transgenic mice




Genotype
MGI:5488619
cx2
Allelic
Composition
E2f1tm1Meg/E2f1+
Tg(CAG-Tfb1m)AGsha/0
Genetic
Background
involves: 129S4/SvJae * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
E2f1tm1Meg mutation (2 available); any E2f1 mutation (28 available)
Tg(CAG-Tfb1m)AGsha mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype



Genotype
MGI:5789744
tg3
Allelic
Composition
Tg(CAG-Tfb1m)AGsha/0
Genetic
Background
B6J.Cg-Tg(CAG-Tfb1m)AGsha
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(CAG-Tfb1m)AGsha mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• 40% reduction in endocochlear potential in 9 to 12 month old mice
• outer hair cells exhibit a positive shift of nearly 20 mV in the voltage at peak capacitance, indicating a mild impairment of voltage-dependent electromotility
• however, hair cells in the apex of the cochlea are intact
• mice exhibit increased latency to peak I at 8 kHz of the ABR at 9-12 months of age but not at 3-6 months of age, indicating dysfunctional cochlear and/or nerve VIII processing only in older mice with hearing loss
• ABR peak I amplitudes are reduced in 9-12 month old mice
• however, central conduction time reflecting synaptic and nerve conduction timing after cochlear/nerve VIII processing is unchanged in mice with severe hearing loss
• ABR thresholds are prematurely elevated
• progressive hearing loss

nervous system
• outer hair cells exhibit a positive shift of nearly 20 mV in the voltage at peak capacitance, indicating a mild impairment of voltage-dependent electromotility
• however, hair cells in the apex of the cochlea are intact




Genotype
MGI:5488618
tg4
Allelic
Composition
Tg(CAG-Tfb1m)AGsha/?
Genetic
Background
involves: C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(CAG-Tfb1m)AGsha mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype




Contributing Projects:
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
11/12/2024
MGI 6.24
The Jackson Laboratory