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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tarbp2tm1.1Dzw
targeted mutation 1.1, Da-Zhi Wang
MGI:5645258
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Tarbp2tm1.1Dzw/Tarbp2tm1.1Dzw
Tg(tetO-Mir208a)#Dzw/?
Tg(Tnnt2-cre)5Blh/?
involves: 129 * C3H * C57BL/6 * DBA/2J MGI:5645730
cn2
Tarbp2tm1.1Dzw/Tarbp2tm1.1Dzw
Tg(Tnnt2-cre)5Blh/0
involves: 129 * C57BL/6 * DBA/2J MGI:5645529


Genotype
MGI:5645730
cn1
Allelic
Composition
Tarbp2tm1.1Dzw/Tarbp2tm1.1Dzw
Tg(tetO-Mir208a)#Dzw/?
Tg(Tnnt2-cre)5Blh/?
Genetic
Background
involves: 129 * C3H * C57BL/6 * DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tarbp2tm1.1Dzw mutation (0 available); any Tarbp2 mutation (22 available)
Tg(tetO-Mir208a)#Dzw mutation (0 available)
Tg(Tnnt2-cre)5Blh mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
N
• transgenic expression of Mir208a prevents the onset of dilated cardiomyopathy in cardiac conditional knockouts of Tarbp2 and results in mice with normal heart morphology, histology, and function




Genotype
MGI:5645529
cn2
Allelic
Composition
Tarbp2tm1.1Dzw/Tarbp2tm1.1Dzw
Tg(Tnnt2-cre)5Blh/0
Genetic
Background
involves: 129 * C57BL/6 * DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tarbp2tm1.1Dzw mutation (0 available); any Tarbp2 mutation (22 available)
Tg(Tnnt2-cre)5Blh mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• Although homozygotes are born in normal mendelian ratio indicating no embryonic lethality, more than 80 percent of these cardiac conditional knockout homozygotes die by 4 months of age and none survive beyond 8 months of age

cardiovascular system
• although gross morphology of the heart is normal at 2 weeks of age, atrial dilation is found by 3 weeks of age and substantial dilation of both atrial and ventricular chambers is found by 1 month of age and is severe in the homozygotes that survive to 2 months of age, yet cardiomyocyte size appears normal
• neonatal adeno-associated virus-mediated delivery of Tarbp2 or transgenic expression of Mir208a suppresses chamber dilation, permits normal cardiac morphology and restores viability as does knockdown of Sox6, while Tnnt2-dirven viral-mediated overexpression of Sox6 recapitulates the phenotype of cardiac conditional null Tarbp2
• by 3 weeks of age atrial dilation is found
• by 1 month of age dilation of the ventricular chambers is also found
• by 2 weeks of age the left ventricular fractional shortening is decreased and this drops precipitously resulting in severe systolic dysfunction by 1 month of age

muscle
• by 2 weeks of age the left ventricular fractional shortening is decreased and this drops precipitously resulting in severe systolic dysfunction by 1 month of age





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory