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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Bag3tm1c(EUCOMM)Hmgu
targeted mutation 1c, Helmholtz Zentrum Muenchen GmbH
MGI:5760384
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Bag3tm1c(EUCOMM)Hmgu/Bag3tm1.1Chen
Tg(Myhca-cre)1Abel/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N * FVB/N MGI:6107910
cn2
Bag3tm1c(EUCOMM)Hmgu/Bag3tm1c(EUCOMM)Hmgu
Tg(CAG-EGFP/Map1lc3b)53Nmz/0
Tg(Myhca-cre)1Abel/0
involves: C57BL/6 * C57BL/6N * C57BL/6NCrlj * DBA/2 * FVB/N MGI:6107905
cn3
Bag3tm1c(EUCOMM)Hmgu/Bag3tm1c(EUCOMM)Hmgu
Tg(Myhca-cre)1Abel/0
involves: C57BL/6N * FVB/N MGI:6107901


Genotype
MGI:6107910
cn1
Allelic
Composition
Bag3tm1c(EUCOMM)Hmgu/Bag3tm1.1Chen
Tg(Myhca-cre)1Abel/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N * FVB/N
Cell Lines HEPD0556_7_B06
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bag3tm1.1Chen mutation (0 available); any Bag3 mutation (31 available)
Bag3tm1c(EUCOMM)Hmgu mutation (2 available); any Bag3 mutation (31 available)
Tg(Myhca-cre)1Abel mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Cardiac enlargement in Bag3tm1c(EUCOMM)Hmgu/Bag3tm1.1Chen Tg(Myhca-cre)1Abel/0 mice at 6 months of age

cardiovascular system
• cardiac enlargement
• heart weight to body weight and heart weight to tibia length ratios are increased at 5 months of age
• diminished systolic function
• diminished systolic function with mice showing reduced fractional shortening, increased left ventricle internal diameter at end diastole and increased left ventricle internal diameter at end systole

homeostasis/metabolism
• hearts exhibit impaired autophagic flux

cellular
• hearts exhibit impaired autophagic flux

muscle
• diminished systolic function

growth/size/body
• cardiac enlargement
• heart weight to body weight and heart weight to tibia length ratios are increased at 5 months of age

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dilated cardiomyopathy 1HH DOID:0110448 OMIM:613881
J:246352




Genotype
MGI:6107905
cn2
Allelic
Composition
Bag3tm1c(EUCOMM)Hmgu/Bag3tm1c(EUCOMM)Hmgu
Tg(CAG-EGFP/Map1lc3b)53Nmz/0
Tg(Myhca-cre)1Abel/0
Genetic
Background
involves: C57BL/6 * C57BL/6N * C57BL/6NCrlj * DBA/2 * FVB/N
Cell Lines HEPD0556_7_B06
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bag3tm1c(EUCOMM)Hmgu mutation (2 available); any Bag3 mutation (31 available)
Tg(CAG-EGFP/Map1lc3b)53Nmz mutation (5 available)
Tg(Myhca-cre)1Abel mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• after 18 hours of starvation, mice exhibit a reduction in LC3-GFP accumulation in the myocardium, indicating suppressed autophagic flux in hearts

homeostasis/metabolism
• after 18 hours of starvation, mice exhibit a reduction in LC3-GFP accumulation in the myocardium, indicating suppressed autophagic flux in hearts




Genotype
MGI:6107901
cn3
Allelic
Composition
Bag3tm1c(EUCOMM)Hmgu/Bag3tm1c(EUCOMM)Hmgu
Tg(Myhca-cre)1Abel/0
Genetic
Background
involves: C57BL/6N * FVB/N
Cell Lines HEPD0556_7_B06
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bag3tm1c(EUCOMM)Hmgu mutation (2 available); any Bag3 mutation (31 available)
Tg(Myhca-cre)1Abel mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Dilated cardiomyopathy in Bag3tm1c(EUCOMM)Hmgu/Bag3tm1c(EUCOMM)Hmgu Tg(Myhca-cre)1Abel/0 mice

homeostasis/metabolism
• neonatal cardiomyocytes exhibit suppression of autophagosome formation following bafilomycin-A1 and chloroquine treatment
• neonatal cardiomyocytes exhibit suppression of autophagosome formation following bafilomycin-A1 and chloroquine treatment indicating impaired autophagy

mortality/aging
• mice are susceptible to premature death, with only 9% of mice surviving past 20 months of age

cardiovascular system
• cardiac enlargement in 6 month old mice
• heart weight to body weight and heart weight to tibia length ratios are increased at 4 months of age
• severe fibrosis in surviving 6 month old mice
• peak rate of pressure rise and peak rate of pressure decline are reduced as early as 10 weeks of age, indicating early impairment of cardiac contractile function
• single myocyte contraction induced by field stimulation is reduced
• however, the profiles of induced calcium transients, including amplitude and tau, are not affected
• neonatal cardiomyocytes exhibit suppression of autophagosome formation following bafilomycin-A1 and chloroquine treatment indicating impaired autophagy
• echocardiography shows an age-dependent decrease in left ventricular systolic function, and left ventricle chamber dilation as evidenced by an increase in end-diastolic left ventricle internal diameter and end-systolic left ventricle internal diameter
• single myocyte contraction induced by field stimulation is reduced

cellular
• neonatal cardiomyocytes exhibit suppression of autophagosome formation following bafilomycin-A1 and chloroquine treatment
• neonatal cardiomyocytes exhibit suppression of autophagosome formation following bafilomycin-A1 and chloroquine treatment indicating impaired autophagy

muscle
• peak rate of pressure rise and peak rate of pressure decline are reduced as early as 10 weeks of age, indicating early impairment of cardiac contractile function
• single myocyte contraction induced by field stimulation is reduced
• however, the profiles of induced calcium transients, including amplitude and tau, are not affected

growth/size/body
• cardiac enlargement in 6 month old mice
• heart weight to body weight and heart weight to tibia length ratios are increased at 4 months of age

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dilated cardiomyopathy 1HH DOID:0110448 OMIM:613881
J:246352





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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