normal phenotype
• viable and fertile with no morphological abnormalities
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Allele Symbol Allele Name Allele ID |
Stk3tm1.1Yy targeted mutation 1.1, Yingzi Yang MGI:4422170 |
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Summary |
8 genotypes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• viable and fertile with no morphological abnormalities
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• following adenoviral cre injection mice are completely protected from TNF alpha or Jo-2 antibody (a Fas agonist) induced mortality
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• following adenoviral cre injection mice are completely protected from TNF alpha induced liver damage
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• following adenoviral cre injection mice are protected from TNF alpha or Jo-2 antibody (a Fas agonist) induced apoptosis
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• following adenoviral cre injection mice are protected from TNF alpha induced increases in ALT levels
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• following adenoviral cre injection mice are protected from TNF alpha induced increases in ALT levels
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• following adenoviral cre injection mice are protected from TNF alpha induced liver damage
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• following adenoviral cre injection mice are protected from TNF alpha or Jo-2 antibody (a Fas agonist) induced apoptosis
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• at 1 - 7 months after tamoxifen treatment
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• some mice treated with tamoxifen at birth develop cholangiocarcinomas composed of mainly multilayered biliary epithelial cells
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• all mice treated with tamoxifen at birth develop tumors which display characteristics of hepatocellular carcinoma by 6 months of age
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• some mice treated with tamoxifen at birth develop cholangiocarcinomas composed of mainly multilayered biliary epithelial cells
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• all mice treated with tamoxifen at birth develop tumors which display characteristics of hepatocellular carcinoma by 6 months of age
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• some mice treated with tamoxifen at birth develop cholangiocarcinomas composed of mainly multilayered biliary epithelial cells
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• in some mice at 1 - 7 months after tamoxifen treatment
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• at 1 - 7 months after tamoxifen treatment
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• in some mice at 1 - 7 months after tamoxifen treatment
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• in some mice at 1 - 7 months after tamoxifen treatment
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• in some mice at 1 - 7 months after tamoxifen treatment
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• at 1 - 7 months after tamoxifen treatment
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• in some mice at 1 - 7 months after tamoxifen treatment
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• slight
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• dysplasia at 1 month of age
• increase in hepatocyte cell density
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• at 1 month of age
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• smaller
• some cells have vacuolated cytoplasm
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• slight
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• at 1 month of age
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• shorter skeletal elements in the limbs
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• shorter skeletal elements in the limbs
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• cell size appears smaller and cell density is increased in the limb cartilage
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• proliferating cells are detected in the hypertrophic zone
• apoptosis is decreased compared to controls
• despite the increase in proliferation and decrease in apoptosis cartilage size is not increased
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• increase in proliferation of cells in the developing limb
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• die between E9.5 and E11.5
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• multiple developmental defects at E9.5 - E10.5
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• at E9.5-E10.5
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• MEFs are resistant to TNF alpha induced apoptosis
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• resistant to TNF alpha induced apoptosis
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• resistant to TNF alpha induced apoptosis
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• at E9.5-E10.5
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• at 12 months of age tumors develop in 2 of 31 mice
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• in untreated mice
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• in untreated mice
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• at 12 months of age tumors develop in 2 of 31 mice
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• following adenoviral cre injection mice are protected from TNF alpha or Jo-2 antibody (a Fas agonist) induced mortality
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• following adenoviral cre injection mice are protected from TNF alpha induced liver damage
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• following adenoviral cre injection mice are protected from TNF alpha or Jo-2 antibody (a Fas agonist) induced apoptosis
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• following adenoviral cre injection mice are mostly protected from TNF alpha induced increases in ALT levels
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• following adenoviral cre injection mice are mostly protected from TNF alpha induced increases in ALT levels
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• following adenoviral cre injection mice are protected from TNF alpha induced liver damage
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• following adenoviral cre injection mice are protected from TNF alpha or Jo-2 antibody (a Fas agonist) induced apoptosis
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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 |
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