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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(WTbeta2)4Wjk
transgene insertion 4, Walter Koch
MGI:3037368
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Gnai2tm1Lbi/Gnai2tm1Lbi
Tg(WTbeta2)4Wjk/0
B6.Cg-Gnai2tm1Lbi Tg(WTbeta2)4Wjk MGI:3799102
cx2
Gnai2tm1Lbi/Gnai2+
Tg(WTbeta2)4Wjk/0
B6.Cg-Gnai2tm1Lbi Tg(WTbeta2)4Wjk MGI:3799103
cx3
Tg(Myh6*)140Lnwd/0
Tg(WTbeta2)4Wjk/0
involves: C57BL/6 * CBA MGI:3799201
cx4
Csrp3tm1Crni/Csrp3tm1Crni
Tg(WTbeta2)4Wjk/0
Not Specified MGI:3037428
tg5
Tg(WTbeta2)4Wjk/0 B6.Cg-Tg(WTbeta2)4Wjk MGI:3799100
tg6
Tg(WTbeta2)4Wjk/0 involves: C57BL/6 MGI:3799200
tg7
Tg(WTbeta2)4Wjk/? Not Specified MGI:3799090


Genotype
MGI:3799102
cx1
Allelic
Composition
Gnai2tm1Lbi/Gnai2tm1Lbi
Tg(WTbeta2)4Wjk/0
Genetic
Background
B6.Cg-Gnai2tm1Lbi Tg(WTbeta2)4Wjk
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gnai2tm1Lbi mutation (1 available); any Gnai2 mutation (54 available)
Tg(WTbeta2)4Wjk mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all pups die between 1 and 4 days after birth
• less then half of the expected Mendelian distribution for pups of this genotype are present at birth

growth/size/body
• pups are smaller than littermate controls at birth

behavior/neurological
• pups are weaker than littermate controls at birth

cardiovascular system
• dilated hearts are found at necropsy of mice that die shortly after birth




Genotype
MGI:3799103
cx2
Allelic
Composition
Gnai2tm1Lbi/Gnai2+
Tg(WTbeta2)4Wjk/0
Genetic
Background
B6.Cg-Gnai2tm1Lbi Tg(WTbeta2)4Wjk
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gnai2tm1Lbi mutation (1 available); any Gnai2 mutation (54 available)
Tg(WTbeta2)4Wjk mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mean survival time is 223 days compared to over 600 for control mice and most mice die by 1 year of age

behavior/neurological
• fatigue occurs in mice with age

cardiovascular system
• the heart to body weight ratio is about twice that of control mice at 7 months of age
• heart appears dilated at necropsy

homeostasis/metabolism
• occurs in mucosal membranes with age
• often found at necropsy
• often found at necropsy

liver/biliary system
• liver congestion is often found at necropsy

respiratory system
• often found at necropsy
• occurs in mice with age

growth/size/body
• the heart to body weight ratio is about twice that of control mice at 7 months of age




Genotype
MGI:3799201
cx3
Allelic
Composition
Tg(Myh6*)140Lnwd/0
Tg(WTbeta2)4Wjk/0
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Myh6*)140Lnwd mutation (0 available)
Tg(WTbeta2)4Wjk mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice have increased mortality with only 50% survival at 8 months and less than 10% survival at 12 months

cardiovascular system
• the heart weight to body weight ratio is 67% greater compared to controls
• fibrosis and cellular disarray are severe in hearts of 8 month old mice
• hearts show dilated ventricular and atrial chambers with thin, fibrotic ventricular walls
• mice have increased fractional shortening at 4 months of age but not 8 months of age
• by 8 months of age, fractional shortening has become significantly impaired to two-thirds of control
• some mice show the signs of congestive heart failure including pulmonary and hepatic enlargement, atrial and ventricular dilation, intraperitoneal edema, and massively enlarged hearts

muscle
• mice have increased fractional shortening at 4 months of age but not 8 months of age
• by 8 months of age, fractional shortening has become significantly impaired to two-thirds of control

growth/size/body
• the heart weight to body weight ratio is 67% greater compared to controls
• fibrosis and cellular disarray are severe in hearts of 8 month old mice
• hearts show dilated ventricular and atrial chambers with thin, fibrotic ventricular walls




Genotype
MGI:3037428
cx4
Allelic
Composition
Csrp3tm1Crni/Csrp3tm1Crni
Tg(WTbeta2)4Wjk/0
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Csrp3tm1Crni mutation (0 available); any Csrp3 mutation (15 available)
Tg(WTbeta2)4Wjk mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• the overexpression of ADRB2 did not influence the dilated cardiomyopathy observed in Csrp3tm1Crni homozygotes

muscle
• the overexpression of ADRB2 did not influence the dilated cardiomyopathy observed in Csrp3tm1Crni homozygotes




Genotype
MGI:3799100
tg5
Allelic
Composition
Tg(WTbeta2)4Wjk/0
Genetic
Background
B6.Cg-Tg(WTbeta2)4Wjk
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(WTbeta2)4Wjk mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mean survival time is 307 days compared to over 600 for control mice and most mice die by 1 year of age

behavior/neurological
• fatigue occurs in mice when approaching 1 year of age

respiratory system
• occurs in mice when approaching 1 year of age

homeostasis/metabolism
• occurs in mucosal membranes as mice approach 1 year of age




Genotype
MGI:3799200
tg6
Allelic
Composition
Tg(WTbeta2)4Wjk/0
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(WTbeta2)4Wjk mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice show increased mortality by one year compared to controls

cardiovascular system
• hearts of 8 month old mice show area of significant fibrosis
• mice have increased fractional shortening at 4 months of age but not 8 months of age
• by 12 months of age, fractional shortening has become significantly impaired

homeostasis/metabolism
• mice have increased exercise tolerance on a treadmill compared to controls at 6 months of age

muscle
• mice have increased fractional shortening at 4 months of age but not 8 months of age
• by 12 months of age, fractional shortening has become significantly impaired




Genotype
MGI:3799090
tg7
Allelic
Composition
Tg(WTbeta2)4Wjk/?
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(WTbeta2)4Wjk mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• loss of mice starts at 8.5 months with a cumulative mortality of 62% by 12 months and 81% by 15 months

growth/size/body
• left ventricle mass is increased indicating left ventricle hypertrophy
• body weight is normal at 4-9 months of age, however mice that die or are sacrificed at 15 months of age have a lower body weight, with wild-type mice showing a 30% increase in body weight compared to mutants

cardiovascular system
• lungs are congested with thickening of alveolar walls and increase in cellular components
• myocytes frequently exhibit polymorphism of nuclei
• hearts show dropout of myocytes and hypertrophy of remaining myocytes
• cross-sectional area of myocytes is 3x greater
• death of cardiac myocytes in areas of fibrosis
• 8-fold increase in collagen content in left ventricles
• left ventricle mass is increased indicating left ventricle hypertrophy
• starting at 9 months of age, mice develop progressive left ventricle dilatation
• hearts show widespread interstitial fibrosis
• interstitial fibrosis is most severe in left ventricular free wall, the apex, the atrio-ventricular junction and perivascular regions
• reduction in fractional shortening after 9 months of age
• wall thickening index of both anterior and posterior walls is lower at 12-15 months, suggesting weakened muscle contraction
• the isometric tension of isolated left atria is three times that of controls while the isometric tension of the right atria is about 75% higher than in wild-type controls
• these parameters at baseline are equal to those observed in control mice maximally stimulated with isoproterenol
• the baseline left ventricle dP/dT-max is 70% higher than in controls
• administration of isoproterenol fails to increase the dP/dTmax as it does in wild-type controls
• this parameter at baseline is equal to those observed in control mice maximally stimulated with isoproterenol
• left ventricle relaxation is enhanced compared to controls with a mean drop in pressure of 5328 mm Hg versus 3313 mm Hg
• echocardiography shows increases in internal and external left ventricle dimensions of diastole, indicating left ventricle dilatation
• the mean heart rate is about 425 bpm compared to 340 bpm in control mice (J:17862)
• there is about a 50% increase in the heart rate of isolated right atria (J:17862)
• ectopic beats mainly occur as singles but occasionally as salvos
• mice exhibit altered configuration of standard lead II ECG waves and development of ectopic beats
• majority of mice exhibit a large Q wave
• majority of mice exhibit suppressed S-T segment
• develops with age
• 17 of 21 mice die of heart failure

homeostasis/metabolism
• higher incidence of chronic thrombus in the left atrium
• higher incidence of pleural effusion
• 8-fold increase in collagen content in left ventricles

muscle
• myocytes frequently exhibit polymorphism of nuclei
• hearts show dropout of myocytes and hypertrophy of remaining myocytes
• cross-sectional area of myocytes is 3x greater
• death of cardiac myocytes in areas of fibrosis
• left ventricle mass is increased indicating left ventricle hypertrophy
• reduction in fractional shortening after 9 months of age
• wall thickening index of both anterior and posterior walls is lower at 12-15 months, suggesting weakened muscle contraction
• the isometric tension of isolated left atria is three times that of controls while the isometric tension of the right atria is about 75% higher than in wild-type controls
• these parameters at baseline are equal to those observed in control mice maximally stimulated with isoproterenol
• the baseline left ventricle dP/dT-max is 70% higher than in controls
• administration of isoproterenol fails to increase the dP/dTmax as it does in wild-type controls
• this parameter at baseline is equal to those observed in control mice maximally stimulated with isoproterenol
• left ventricle relaxation is enhanced compared to controls with a mean drop in pressure of 5328 mm Hg versus 3313 mm Hg
• develops with age

respiratory system
• lungs are congested with thickening of alveolar walls and increase in cellular components
• higher incidence of pleural effusion

cellular
• hearts show widespread interstitial fibrosis
• interstitial fibrosis is most severe in left ventricular free wall, the apex, the atrio-ventricular junction and perivascular regions





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory