Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Casp8tm1.1Yuan mutation
(0 available);
any
Casp8 mutation
(42 available)
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mortality/aging
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• homozygotes exhibit no differences from homozygous Casp8tm1Yuan mutants in the kinetics of prenatal death, however no data is presented in J:49459
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cardiovascular system
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• homozygotes show no differences in the gross phenotype from homozygous Casp8tm1Yuan, however no data is presented in J:49459
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growth/size/body
embryo
hematopoietic system
muscle
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Casp8tm1.1Yuan mutation
(0 available);
any
Casp8 mutation
(42 available)
Casp8tm1Wll mutation
(0 available);
any
Casp8 mutation
(42 available)
Tg(Mx1-cre)1Cgn mutation
(7 available)
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mortality/aging
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• unlike mice that do not carry Casp8tm1.1Yuan, compound heterozygous mutants survive injection with an anti-Fas Ab
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hematopoietic system
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• 2 days after induction of cre expression the ability of progenitor cells to form myeloid or B lymphoid colonies in culture or in transplant studies is significantly decreased
• the ability of these progenitors to differentiate into macrophages is also decreased after induction of cre expression
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|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Casp8tm1.1Yuan mutation
(0 available);
any
Casp8 mutation
(42 available)
Casp8tm1Wll mutation
(0 available);
any
Casp8 mutation
(42 available)
Tg(Alb1-cre)7Gsc mutation
(1 available)
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mortality/aging
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• unlike mice that do not carry Casp8tm1.1Yuan, compound heterozygous mutants survive after injection with an anti-Fas Ab
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homeostasis/metabolism
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Casp8tm1.1Yuan mutation
(0 available);
any
Casp8 mutation
(42 available)
Casp8tm1Wll mutation
(0 available);
any
Casp8 mutation
(42 available)
Tg(Tie1-cre)9Ref mutation
(2 available)
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mortality/aging
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• compound heterozygotes die around E12, similar to Casp8tm1.1Yuan homozygotes
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cellular
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• extensive necrosis of the cardiomyocytes in the ventricles and atria is seen
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cardiovascular system
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• the density of the vasculature in the yolk sac is decreased
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• severe congestion of the liver and large vessels of the chest and abdomen similar to Casp8tm1.1Yuan homozygotes is seen
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• extensive necrosis of the cardiomyocytes in the ventricles and atria is seen
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• the heart has a globose shape
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• around E12 thin and occasionally ruptured ventricular walls are seen
• heart defects are not seen in mutants at E10-E11.5
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• around E12, the pericardial space is enlarged consistent with pericardial edema
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muscle
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• extensive necrosis of the cardiomyocytes in the ventricles and atria is seen
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embryo
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• the density of the vasculature in the yolk sac is decreased
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• an undulated neural tube is seen
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• the density of the vasculature and amount of blood in the yolk sac is decreased
• increased cell death is seen in the yolk sac at E10.5 even when no signs of vascular degeneration were detected
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hematopoietic system
N |
• hematopoietic progenitor numbers are not decreased unlike in Casp8tm1.1Yuan homozygotes
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homeostasis/metabolism
nervous system
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• an undulated neural tube is seen
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Casp8tm1.1Yuan mutation
(0 available);
any
Casp8 mutation
(42 available)
Casp8tm1Wll mutation
(0 available);
any
Casp8 mutation
(42 available)
Lyz2tm1(cre)Ifo mutation
(14 available);
any
Lyz2 mutation
(41 available)
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hematopoietic system
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• the number monocyte progenitors is not decreased; however, recombined progenitors can not differentiate into macrophages
• the ability of bone marrow progenitors to differentiate into granulocytes is not impaired
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immune system
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• the number monocyte progenitors is not decreased; however, recombined progenitors can not differentiate into macrophages
• the ability of bone marrow progenitors to differentiate into granulocytes is not impaired
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cellular
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• the number monocyte progenitors is not decreased; however, recombined progenitors can not differentiate into macrophages
• the ability of bone marrow progenitors to differentiate into granulocytes is not impaired
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