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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
U2af1tm1.1Hev
targeted mutation 1.1, Harold E Varmus
MGI:6202047
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Runx1tm3Spe/Runx1tm3Spe
U2af1tm1.1Hev/U2af1+
Tg(Mx1-cre)1Cgn/0
involves: 129S4/SvJae * 129S6/SvEvTac * BALB/c * C57BL/6 * CBA/J MGI:6273496
cn2
Tg(Mx1-cre)1Cgn/0
U2af1tm1.1Hev/U2af1+
involves: 129S6/SvEvTac * BALB/c * C57BL/6 * C57BL/6J * CBA/J MGI:6273483


Genotype
MGI:6273496
cn1
Allelic
Composition
Runx1tm3Spe/Runx1tm3Spe
U2af1tm1.1Hev/U2af1+
Tg(Mx1-cre)1Cgn/0
Genetic
Background
involves: 129S4/SvJae * 129S6/SvEvTac * BALB/c * C57BL/6 * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Runx1tm3Spe mutation (0 available); any Runx1 mutation (35 available)
Tg(Mx1-cre)1Cgn mutation (7 available)
U2af1tm1.1Hev mutation (1 available); any U2af1 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• poly (IC) treated mice develop multilineage cytopenia
• mice develop low-level myeloid dysplasia after poly (IC) treatment
• mice develop thrombocytopenia after poly (IC) treatment
• mice exhibit an increased percentage of myeloid cells and increased myeloid colony formation after poly (IC) treatment
• mice develop low-level erythroid dysplasia after poly (IC) treatment

homeostasis/metabolism
• one mouse treated with ENU after poly (IC) treatment developed acute myeloid leukemia
• mice treated with ENU after poly (IC) treatment exhibit increased percentages of myeloid cells in the peripheral blood, enlarged spleen, and extramedullary hematopoiesis, occasional low-grade dysplasia in the erythroid and neutrophil lineages indicating the development of myeloproliferative neoplasm

mortality/aging
N
• poly (IC) treated mice have a normal life span and do not develop frank leukemia within 1.5 years after poly (IC) treatment
• mice treated with ENU after poly (IC) treatment die prematurely with myeloid pathology

neoplasm
• one mouse treated with ENU after poly (IC) treatment developed acute myeloid leukemia
• mice treated with ENU after poly (IC) treatment exhibit increased percentages of myeloid cells in the peripheral blood, enlarged spleen, and extramedullary hematopoiesis, occasional low-grade dysplasia in the erythroid and neutrophil lineages indicating the development of myeloproliferative neoplasm




Genotype
MGI:6273483
cn2
Allelic
Composition
Tg(Mx1-cre)1Cgn/0
U2af1tm1.1Hev/U2af1+
Genetic
Background
involves: 129S6/SvEvTac * BALB/c * C57BL/6 * C57BL/6J * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Mx1-cre)1Cgn mutation (7 available)
U2af1tm1.1Hev mutation (1 available); any U2af1 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• mice exhibit a mild reduction in red blood cell count and increase in mean red blood cell volume after poly (IC) treatment, indicating macrocytic anemia
• binucleated erythroid cells and hypo-segmented neutrophils are seen in the bone marrow cells occasionally in poly (IC) treated mice
• megakaryocytes occasionally form clusters in poly (IC) treated mice
• these dysplastic features affect less than 1% of bone marrow cells and are not seen in the peripheral blood
• mice show a mild reduction in red blood cell count after poly (IC) treatment
• however, platelet numbers are normal, bone marrow cellularity and spleen size are normal after poly (IC) treatment
• mice show a mild reduction in hematocrit after poly (IC) treatment
• mice show a mild reduction in hemoglobin concentration after poly (IC) treatment
• mice show a mild increase in mean corpuscular volume after poly (IC) treatment
• poly (IC) treated mice show a nearly 50% reduction in numbers of white blood cells, with decreases in all major lineages and the most marked reduction in B220+ B cells
• the hematopoietic stem cell- and progenitor-enriched LSK cells (Lin-Sca-1+C-Kit+) are decreased in the bone marrow at 36 weeks after poly (IC) treatment; decrease in the LSK cells is due to the reduction of short-term and long-term HSCs (CD48-CD150- and CD48-CD150+, respectively) but not the multipotent progenitors in the bone marrow
• however, no differences are seen in the percentages of Lin- cells and MPs after poly (IC) treatment

immune system
• poly (IC) treated mice show a nearly 50% reduction in numbers of white blood cells, with decreases in all major lineages and the most marked reduction in B220+ B cells

mortality/aging
N
• poly (IC) treated mice exhibit a normal life span

neoplasm
N
• mice do not develop leukemia following poly (IC) treatment





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory