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Phenotypes Associated with This Genotype
Genotype
MGI:5295465
Allelic
Composition
Ptpn11tm1Ckq/Ptpn11+
Tg(Mx1-cre)1Cgn/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptpn11tm1Ckq mutation (0 available); any Ptpn11 mutation (43 available)
Tg(Mx1-cre)1Cgn mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Increased spleen weight in Ptpn11tm1Ckq/Ptpn11+ Tg(Mx1-cre)1Cgn/0 mice

mortality/aging
• by 56 weeks due to leukemia in pIpC-treated mice

hematopoietic system
• T cell lymphoblastic leukemia/lymphoma in 9 of 27 pIpC-treated mice
• in pIpC-treated mice
• in pIpC-treated mice
• around the pro-B stage in pIpC-treated mice
• 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
• hyperproliferation in the liver and spleen in pIpC-treated mice
• progressive in pIpC-treated mice
• 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
• extremely high after 32 weeks with leukemia infiltration in nonhematopoietic organs of pIpC-treated mice
• in pIpC-treated mice
• 3-fold in the bone marrow in pIpC-treated mice
• in the spleen of pIpC-treated mice
• 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

neoplasm
• T cell lymphoblastic leukemia/lymphoma in 9 of 27 pIpC-treated mice
• after 12 to 32 weeks of chronic myeloproliferative disease in pIpC-treated mice
• B and T cell lymphoblastic leukemia/lymphoma in pIpC-treated mice
• acute myeloid leukemia in 6 of 27 pIpC-treated mice
• B cell lymphoblastic leukemia/lymphoma in 2 of 27 pIpC-treated mice

cellular
• in bone marrow cells and splenocytes from pIpC-treated mice
• in pIpC-treated mice due to centrosome amplification

liver/biliary system
• in pIpC-treated mice

immune system
• T cell lymphoblastic leukemia/lymphoma in 9 of 27 pIpC-treated mice
• in pIpC-treated mice
• in pIpC-treated mice
• around the pro-B stage in pIpC-treated mice
• 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
• extremely high after 32 weeks with leukemia infiltration in nonhematopoietic organs of pIpC-treated mice
• in pIpC-treated mice

endocrine/exocrine glands
• T cell lymphoblastic leukemia/lymphoma in 9 of 27 pIpC-treated mice

growth/size/body
• in pIpC-treated mice
• in pIpC-treated mice
• in pIpC-treated mice


Contributing Projects:
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
01/06/2026
MGI 6.24
The Jackson Laboratory