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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Yap1tm1.1Eno
targeted mutation 1.1, Eric N Olson
MGI:5446483
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Yap1tm1.1Eno/Yap1tm1.1Eno
Nkx2-5tm1(cre)Rjs/Nkx2-5+
involves: 129S/SvEv MGI:5446510
cn2
Wwtr1tm1.1Eno/Wwtr1tm1.1Eno
Yap1tm1.1Eno/Yap1tm1.1Eno
Tg(Myh6-cre)2182Mds/0
involves: 129S/SvEv * FVB/N MGI:5544298
cn3
Wwtr1tm1.1Eno/Wwtr1+
Yap1tm1.1Eno/Yap1tm1.1Eno
Tg(Myh6-cre)2182Mds/0
involves: 129S/SvEv * FVB/N MGI:5544297
cn4
Wwtr1tm1.1Eno/Wwtr1tm1.1Eno
Yap1tm1.1Eno/Yap1+
Tg(Myh6-cre)2182Mds/0
involves: 129S/SvEv * FVB/N MGI:5544296
cn5
Yap1tm1.1Eno/Yap1tm1.1Eno
Tg(Myh6-cre)2182Mds/0
involves: 129S/SvEv * FVB/N MGI:5544295


Genotype
MGI:5446510
cn1
Allelic
Composition
Yap1tm1.1Eno/Yap1tm1.1Eno
Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic
Background
involves: 129S/SvEv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nkx2-5tm1(cre)Rjs mutation (1 available); any Nkx2-5 mutation (21 available)
Yap1tm1.1Eno mutation (0 available); any Yap1 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

cardiovascular system
• abnormally thin myocardium
• ventricular myocyte number is significantly reduced
• cardiac looping and chamber formation are normal
• slower heart beat at E9.5
• mice are normal at E8.5

muscle
• abnormally thin myocardium
• ventricular myocyte number is significantly reduced
• cardiac looping and chamber formation are normal




Genotype
MGI:5544298
cn2
Allelic
Composition
Wwtr1tm1.1Eno/Wwtr1tm1.1Eno
Yap1tm1.1Eno/Yap1tm1.1Eno
Tg(Myh6-cre)2182Mds/0
Genetic
Background
involves: 129S/SvEv * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Myh6-cre)2182Mds mutation (3 available)
Wwtr1tm1.1Eno mutation (0 available); any Wwtr1 mutation (26 available)
Yap1tm1.1Eno mutation (0 available); any Yap1 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Wwtr1tm1.1Eno/Wwtr1tm1.1Eno Yap1tm1.1Eno/Yap1tm1.1Eno Tg(Myh6-cre)2182Mds/0 mice exhibit cardiac abnormalities and Wwtr1tm1.1Eno/Wwtr1+ Yap1tm1.1Eno/Yap1tm1.1Eno Tg(Myh6-cre)2182Mds/0 hearts show defects in proliferation and survival

mortality/aging

cardiovascular system
• severe cardiac defects




Genotype
MGI:5544297
cn3
Allelic
Composition
Wwtr1tm1.1Eno/Wwtr1+
Yap1tm1.1Eno/Yap1tm1.1Eno
Tg(Myh6-cre)2182Mds/0
Genetic
Background
involves: 129S/SvEv * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Myh6-cre)2182Mds mutation (3 available)
Wwtr1tm1.1Eno mutation (0 available); any Wwtr1 mutation (26 available)
Yap1tm1.1Eno mutation (0 available); any Yap1 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Cardiomyopathy in Wwtr1tm1.2Eno/Wwtr1+ Yap1tm1.1Eno/Yap1tm1.1Eno Tg(Myh6-cre)2182Mds/0 mice

mortality/aging
• die by 10 days of age
• lethality is accelerated compared to mutant mice wild type for Wwtr1

cardiovascular system
• about a 60% decrease in the number of cardiomyocytes

cellular

muscle
• about a 60% decrease in the number of cardiomyocytes




Genotype
MGI:5544296
cn4
Allelic
Composition
Wwtr1tm1.1Eno/Wwtr1tm1.1Eno
Yap1tm1.1Eno/Yap1+
Tg(Myh6-cre)2182Mds/0
Genetic
Background
involves: 129S/SvEv * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Myh6-cre)2182Mds mutation (3 available)
Wwtr1tm1.1Eno mutation (0 available); any Wwtr1 mutation (26 available)
Yap1tm1.1Eno mutation (0 available); any Yap1 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Cardiomyopathy in Wwtr1tm1.2Eno/Wwtr1tm1.2Eno Yap1tm1.1Eno/Yap1+ Tg(Myh6-cre)2182Mds/0 mice

mortality/aging
• complete lethality by 33 weeks of age from heart failure

cardiovascular system
• grossly dilated at 30 weeks of age but seen as early as 8 days of age

homeostasis/metabolism
• at 30 weeks of age

muscle
• grossly dilated at 30 weeks of age but seen as early as 8 days of age




Genotype
MGI:5544295
cn5
Allelic
Composition
Yap1tm1.1Eno/Yap1tm1.1Eno
Tg(Myh6-cre)2182Mds/0
Genetic
Background
involves: 129S/SvEv * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Myh6-cre)2182Mds mutation (3 available)
Yap1tm1.1Eno mutation (0 available); any Yap1 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Lethal cardiomyopathy in Yap1tm1.1Eno/Yap1tm1.1Eno Tg(Myh6-cre)2182Mds/0 mice

mortality/aging
• die between 11 and 20 weeks of age from heart failure

cardiovascular system
• develops by 9 weeks of age
• mild dilation is seen at 6 weeks of age and becomes more pronounced at 12 weeks of age
• develops in older mice with dilated cardiomyopathy
• mild functional heart deficits by 6 weeks of age
• develops by 9 weeks of age and worsens with age
• mild at 6 weeks of age and becomes more pronounced at 12 weeks of age
• at 26 days after permanent ligation of the left anterior descending coronary artery at P2, mice display a gross deficiency of healthy myocardial tissue throughout the LV free wall and extensive fibrotic infarct zone unlike controls that have fully regenerated by this time

behavior/neurological
• become lethargic between 11 and 20 weeks of age

respiratory system
• develops between 11 and 20 weeks of age

homeostasis/metabolism
• at 26 days after permanent ligation of the left anterior descending coronary artery at P2, mice display a gross deficiency of healthy myocardial tissue throughout the LV free wall and extensive fibrotic infarct zone unlike controls that have fully regenerated by this time
• develops in older mice with dilated cardiomyopathy

muscle
• develops by 9 weeks of age and worsens with age
• mild at 6 weeks of age and becomes more pronounced at 12 weeks of age





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