Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
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hematopoietic system
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• impairment of normal hematopoiesis
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neoplasm
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• mutants develop myeloid leukemia resembling human t(11;17) acute promyelocytic leukemia, showing an accumulation of immature myeloblastic cells in hematopoietic tissues and infiltration of nonhematopoietic organs, including the liver, lung, gastrointestinal tract, and kidney
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
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neoplasm
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• 6 of 51 founders develop leukemia, usually with short latent periods of 31-85 days after birth
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• develop chronic myeloid leukemia-like phenotypes within 3 months of life
• mutants with leukemia show an increased percentage of mature myeloid cells and myeloid/lymphoid ratio in the peripheral blood and bone marrow resembling chronic myeloid leukemia
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growth/size/body
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• mutants with leukemia have low body weight
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• mutants with leukemia exhibit splenomegaly
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hematopoietic system
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• about 20% increase in promyelocytes
• extreme expansion of myeloid cells at varying stages of maturation
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• extreme expansion of myeloid cells at varying stages of maturation
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• follicular architecture is damaged
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• mutants with leukemia exhibit splenomegaly
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• red pulp is infiltrated by myeloid cells, mainly myelocytes, metamyelocytes, and segmented forms
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• all-trans-retinoic acid treatment does not induce bone marrow cells to differentiate as in controls
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immune system
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• about 20% increase in promyelocytes
• extreme expansion of myeloid cells at varying stages of maturation
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• extreme expansion of myeloid cells at varying stages of maturation
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• follicular architecture is damaged
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• mutants with leukemia exhibit splenomegaly
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• red pulp is infiltrated by myeloid cells, mainly myelocytes, metamyelocytes, and segmented forms
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liver/biliary system
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• focal infiltration of liver with myeloid precursors, however gross structure of the liver is unaffected
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skeleton
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• disruption of bone marrow trabeculae
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