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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Runx1tm1Soga
targeted mutation 1, Seishi Ogawa
MGI:3036550
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Runx1tm1Soga/Runx1tm1.1Soga
Tg(Mx1-cre)1Cgn/0
involves: C57BL/6 * CBA MGI:3036555
cn2
Runx1tm1Soga/Runx1tm1Soga
Stag2tm1.1Soga/Y
Tg(Mx1-cre)1Cgn/0
involves: C57BL/6J * C57BL/6N * CBA/J MGI:6696300


Genotype
MGI:3036555
cn1
Allelic
Composition
Runx1tm1Soga/Runx1tm1.1Soga
Tg(Mx1-cre)1Cgn/0
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Runx1tm1.1Soga mutation (0 available); any Runx1 mutation (34 available)
Runx1tm1Soga mutation (0 available); any Runx1 mutation (34 available)
Tg(Mx1-cre)1Cgn mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
N
• mutants injected with pIpC to induce expression of Cre recombinase exhibit normal myeloid cell development, neutrophil counts, hemoglobin levels, and maintenance of hematopoietic stem cells in adults
• pIpC treated mutants exhibit an increase in apoptosis of myeloid colony-forming cells
• pIpC treated mutants exhibit a significant block in the maturation of T-cell progenitors at the transition from CD44+CD25+ (double negative 2) to CD44-CD25+ (double negative 3), indicating the accumulation of immature T-cell precursors in the thymus
• the immature megakaryocytes observed in bone marrow of mutants injected with pIpC exhibit poorly demarcated membranes and a lower level of polyploidy than controls
• after injection of pIpC to induce expression of Cre recombinase, bone marrow exhibits an arrest in megakaryocytic maturation
• after injection of pIpC to induce expression of Cre recombinase, mutants exhibit an increase in hematopoietic progenitor cells
• bone marrow cells from pIpC injected mutants form more megakaryocytic (CFU-Meg), myeloid, and mixed (myeloid and erythroid) colonies in vitro than control bone marrow cells
• immediately after injection of pIpC to induce expression of Cre recombinase, mice show a decline in platelet counts to 1/3 to 1/6 of those for the control

immune system
• pIpC treated mutants exhibit a significant block in the maturation of T-cell progenitors at the transition from CD44+CD25+ (double negative 2) to CD44-CD25+ (double negative 3), indicating the accumulation of immature T-cell precursors in the thymus

cellular
• after injection of pIpC to induce expression of Cre recombinase, bone marrow exhibits an arrest in megakaryocytic maturation




Genotype
MGI:6696300
cn2
Allelic
Composition
Runx1tm1Soga/Runx1tm1Soga
Stag2tm1.1Soga/Y
Tg(Mx1-cre)1Cgn/0
Genetic
Background
involves: C57BL/6J * C57BL/6N * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Runx1tm1Soga mutation (0 available); any Runx1 mutation (34 available)
Stag2tm1.1Soga mutation (0 available); any Stag2 mutation (15 available)
Tg(Mx1-cre)1Cgn mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• lethally irradiated mice transplanted with mutant bone marrow cells followed by pIpC injection develop anemia with increased mean corpuscular volume and red blood cell distribution width
• lethally irradiated mice transplanted with mutant bone marrow cells followed by pIpC injection exhibit reduced white blood cell count, with a reduction in lymphocytes, granulocytes, and monocytes
• lethally irradiated mice transplanted with mutant bone marrow cells followed by pIpC injection exhibit increased frequency of immature bone marrow progenitors (LSK cells)
• lethally irradiated mice transplanted with mutant bone marrow cells followed by pIpC injection exhibit lineage-committed mature cells that are skewed to myeloid lineages
• lethally irradiated mice transplanted with mutant bone marrow cells followed by pIpC injection show reduced frequency of colony-forming unit erythroid cells and Ter119+CD71+ erythroid progenitors
• lethally irradiated mice transplanted with mutant bone marrow cells followed by pIpC injection show increased mean corpuscular volume
• lethally irradiated mice transplanted with mutant bone marrow cells followed by pIpC injection show increased red blood cell distribution width
• all lethally irradiated mice transplanted with mutant-derived bone marrow, followed by pIpC injection, develop overt myelodysplastic syndrome, mostly within half a year after pIpC injection, with severe cytopenia and marked trilineage dysplasia

immune system
• lethally irradiated mice transplanted with mutant bone marrow cells followed by pIpC injection exhibit reduced white blood cell count, with a reduction in lymphocytes, granulocytes, and monocytes





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory