Allele Symbol Allele Name Allele ID |
Ptpn11tm1Ckq targeted mutation 1, Cheng-Kui Qu MGI:5295460 |
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Summary |
6 genotypes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• B cell lymphoblastic leukemia/lymphoma in 4 of 9 mice
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• B cell lymphoblastic leukemia/lymphoma in 4 of 9 mice
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• acute myeloid leukemia in 4 of 10 mice
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• all mice develop myeloproliferative disease with enhanced myeloid cell proliferation and differentiation
• 2 of 10 mice develop accelerated myeloproliferative disease
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• all mice develop myeloproliferative disease with enhanced myeloid cell proliferation and differentiation
• 2 of 10 mice develop accelerated myeloproliferative disease
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• mice die around E11.5
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• at E9.5
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• enlarged
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• at E9.5
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• by 56 weeks due to leukemia in pIpC-treated mice
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• T cell lymphoblastic leukemia/lymphoma in 9 of 27 pIpC-treated mice
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• in pIpC-treated mice
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• in pIpC-treated mice
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• around the pro-B stage in pIpC-treated mice
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• all pIpC-treated mice develop myeloproliferative disease (MPD)
• Mac-1+/Gr-1+ mature myeloid cells are increased
• 5 of 27 pIpC-treated mice exhibit accelerated MPD
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• hyperproliferation in the liver and spleen in pIpC-treated mice
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• pIpC-treated mice exhibit decreased common myeloid progenitors, granulocyte macrophage progenitors, and megakaryocyte erythroid progenitors compared with wild-type mice
• however, common lymphoid progenitor numbers are normal
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• in pIpC-treated mice
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• extremely high after 32 weeks with leukemia infiltration in nonhematopoietic organs of pIpC-treated mice
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• in pIpC-treated mice
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• 3-fold in the bone marrow in pIpC-treated mice
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• in the spleen of pIpC-treated mice
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• hematopoietic stem cells are hyperactivated in pIpC-treated mice
• hematopoietic stem cell quiescent in pIpC-treated mice is decreased 2-fold while the S and G2/M phase were doubled compared to in wild-type mice
• apoptosis of hematopoietic stem cells in pIpC-treated mice is decreased compared to in wild-type mice
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• T cell lymphoblastic leukemia/lymphoma in 9 of 27 pIpC-treated mice
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• after 12 to 32 weeks of chronic myeloproliferative disease in pIpC-treated mice
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• B and T cell lymphoblastic leukemia/lymphoma in pIpC-treated mice
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• acute myeloid leukemia in 6 of 27 pIpC-treated mice
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• B cell lymphoblastic leukemia/lymphoma in 2 of 27 pIpC-treated mice
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• in bone marrow cells and splenocytes from pIpC-treated mice
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• in pIpC-treated mice due to centrosome amplification
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• in pIpC-treated mice
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• T cell lymphoblastic leukemia/lymphoma in 9 of 27 pIpC-treated mice
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• in pIpC-treated mice
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• in pIpC-treated mice
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• around the pro-B stage in pIpC-treated mice
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• all pIpC-treated mice develop myeloproliferative disease (MPD)
• Mac-1+/Gr-1+ mature myeloid cells are increased
• 5 of 27 pIpC-treated mice exhibit accelerated MPD
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• extremely high after 32 weeks with leukemia infiltration in nonhematopoietic organs of pIpC-treated mice
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• in pIpC-treated mice
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• T cell lymphoblastic leukemia/lymphoma in 9 of 27 pIpC-treated mice
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• in pIpC-treated mice
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• in pIpC-treated mice
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• in pIpC-treated mice
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• T cell lymphoblastic leukemia/lymphoma in 8 of 15 mice
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• T cell lymphoblastic leukemia/lymphoma in 8 of 15 mice
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• T cell lymphoblastic leukemia/lymphoma in 8 of 15 mice
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N |
• T and B cell development is normal
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• T cell lymphoblastic leukemia/lymphoma in 8 of 15 mice
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• T cell lymphoblastic leukemia/lymphoma in 8 of 15 mice
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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 11/19/2024 MGI 6.24 |
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