immune system
• consistent but not statistically significant
|
Allele Symbol Allele Name Allele ID |
Cd247tm2.1Lov targeted mutation 2.1, Paul E Love MGI:5468025 |
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Summary |
4 genotypes
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|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• consistent but not statistically significant
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
N |
• mice do not develop spontaneous autoimmune disease
|
• depending on the nature of the negative selecting interaction, thymocytes exhibit impaired negative selection compared with control mice
• mice exhibit an increase in regulatory T cell numbers due to increased generation of thymus-derived T regulatory cells
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• ex vivo and after in vitro stimulation, CD4+ T cells exhibit significant skewing to Th1 compared with control cell
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• impaired development
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• in the thymus and periphery
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• in the thymus and periphery
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• in the thymus, lymph nodes and spleen due to increased generation of thymus-derived T regulatory cells
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• impaired development
|
• mice exhibit increased T cells with memory-like phenotype that proliferate in vivo compared with control mice
• regulatory T cells exhibit enhanced suppressive activity to suppress the proliferation of effector T cells
|
• double-positive thymocytes are resistant to anti-CD3 and anti-CD28-induced apoptosis compared with control cells
|
• in the thymus, lymph nodes and spleen due to increased generation of thymus-derived T regulatory cells
|
• double-positive thymocytes are resistant to anti-CD3 and anti-CD28-induced apoptosis compared with control cells
|
• depending on the nature of the negative selecting interaction, thymocytes exhibit impaired negative selection compared with control mice
• mice exhibit an increase in regulatory T cell numbers due to increased generation of thymus-derived T regulatory cells
|
• ex vivo and after in vitro stimulation, CD4+ T cells exhibit significant skewing to Th1 compared with control cell
|
• impaired development
|
• in the thymus and periphery
|
• in the thymus and periphery
|
• in the thymus, lymph nodes and spleen due to increased generation of thymus-derived T regulatory cells
|
• impaired development
|
• mice exhibit increased T cells with memory-like phenotype that proliferate in vivo compared with control mice
• regulatory T cells exhibit enhanced suppressive activity to suppress the proliferation of effector T cells
|
• double-positive thymocytes are resistant to anti-CD3 and anti-CD28-induced apoptosis compared with control cells
|
• in the thymus, lymph nodes and spleen due to increased generation of thymus-derived T regulatory cells
|
• bone marrow cells transplanted into Rag1 null mice induce autoimmune disorder with increased incidence of inflammatory lesions and anti-nuclear antibodies compared when control bone marrow cells are transplanted
• however, mice do not develop spontaneous autoimmune disease
|
• double-positive thymocytes are resistant to anti-CD3 and anti-CD28-induced apoptosis compared with control cells
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
N |
• mice do not develop spontaneous autoimmune disease
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• thymocyte negative selection in response to ubiquitous male antigen is impaired, but not abrogated, compared to in control mice
|
• thymocyte negative selection in response to ubiquitous male antigen is impaired, but not abrogated, compared to in control mice
|
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 12/17/2024 MGI 6.24 |
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