immune system
N |
• mice exhibit normal numbers of double negative, double positive, CD4 single positive and CD8 single positive T cells
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Allele Symbol Allele Name Allele ID |
Hdac1tm1.1Shmc targeted mutation 1.1, Shaun M Cowley MGI:5485390 |
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Summary |
4 genotypes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
N |
• mice exhibit normal numbers of double negative, double positive, CD4 single positive and CD8 single positive T cells
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|
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
N |
• mice exhibit normal numbers of double negative, double positive, CD4 single positive and CD8 single positive T cells
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• all mice die at an average of 15 weeks
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• in neonates and at 6 weeks
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• in the thymus and spleen
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• effacement of medullary and cortical substructures in diseased thymus
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• massively in diseased mice due to overpopulation with immature and double positive T cells
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• 2-fold reduction in mature TCRbetahigh/CD5high thymocytes at 10 to 14 days
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• 3-fold increase immature TCRbetaint/CD5low thymocytes at 10 to 14 days
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• massively in diseased mice due to overpopulation with immature and double positive T cells
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• 2.6-fold reduction at 10 to 14 days
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• increase in CD4low/CD8high cells at 6 to 8 weeks
• 10-fold increase in absolute number of CD4low/CD8high cells at 10 to 14 days
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• block at the double negative to double positive transition
• defects in positive selection and CD4 lineage commitment
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• 4-fold increase in the percent of immature single positive cells at 6 to 8 weeks
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• with general hyperproliferation of immature T cells and infiltration into nonlymphatic organs (lung, liver and kidney)
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• in moribund mice
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• in moribund mice
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• massively in diseased mice due to overpopulation with immature and double positive T cells
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• in moribund mice
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• in tumor cells
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• in neonates and at 6 weeks
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• in the thymus and spleen
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• in tumorigenic T cells
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• in neonates and at 6 weeks
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• in the thymus and spleen
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• effacement of medullary and cortical substructures in diseased thymus
|
• massively in diseased mice due to overpopulation with immature and double positive T cells
|
• 2-fold reduction in mature TCRbetahigh/CD5high thymocytes at 10 to 14 days
|
• 3-fold increase immature TCRbetaint/CD5low thymocytes at 10 to 14 days
|
• massively in diseased mice due to overpopulation with immature and double positive T cells
|
• 2.6-fold reduction at 10 to 14 days
|
• increase in CD4low/CD8high cells at 6 to 8 weeks
• 10-fold increase in absolute number of CD4low/CD8high cells at 10 to 14 days
|
• block at the double negative to double positive transition
• defects in positive selection and CD4 lineage commitment
|
• 4-fold increase in the percent of immature single positive cells at 6 to 8 weeks
|
• in neonates and at 6 weeks
|
• effacement of medullary and cortical substructures in diseased thymus
|
• massively in diseased mice due to overpopulation with immature and double positive T cells
|
• 2-fold reduction in mature TCRbetahigh/CD5high thymocytes at 10 to 14 days
|
• 3-fold increase immature TCRbetaint/CD5low thymocytes at 10 to 14 days
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• all mice die at an average of 15 weeks
|
• in diseased mice
|
• 5-fold reduction in cellularity in neonates
|
• in diseased mice
|
• in the percentage but not the absolute numbers
|
• increase in CD4low/CD8high cells at 6 to 8 weeks
|
• block at the double negative to double positive transition
|
• 4-fold increase in the percent of immature single positive cells at 6 to 8 weeks
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• in 1 of 8 mice
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• in moribund mice
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• in moribund mice
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• in diseased mice
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• in moribund mice
|
• in diseased mice
|
• 5-fold reduction in cellularity in neonates
|
• in diseased mice
|
• in the percentage but not the absolute numbers
|
• increase in CD4low/CD8high cells at 6 to 8 weeks
|
• block at the double negative to double positive transition
|
• 4-fold increase in the percent of immature single positive cells at 6 to 8 weeks
|
• in diseased mice
|
• 5-fold reduction in cellularity in neonates
|
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 12/10/2024 MGI 6.24 |
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