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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mybl2tm1.1Epr
targeted mutation 1.1, E Premkumar Reddy
MGI:5577181
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Mybl2tm1.1Epr/Mybl2tm1.1Epr
Tg(Mx1-cre)1Cgn/0
involves: 129X1/SvJ * C57BL/6 * CBA * FVB/N MGI:5577184


Genotype
MGI:5577184
cn1
Allelic
Composition
Mybl2tm1.1Epr/Mybl2tm1.1Epr
Tg(Mx1-cre)1Cgn/0
Genetic
Background
involves: 129X1/SvJ * C57BL/6 * CBA * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mybl2tm1.1Epr mutation (0 available); any Mybl2 mutation (114 available)
Tg(Mx1-cre)1Cgn mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• in lethally irradiated host when transplanted with bone marrow cells
• decreased number and increased fraction of apoptotic common myeloid progenitors granulocyte-monocyte progenitors and megakaryocyte-erythroid progenitors following pIpC treatment
• decreased myeloid cells in bone marrow and spleen at 21 days post pIpC treatment every other day for 5 days
• impact on myeloid compartment is more profound than B and T cell compartments
• at 21 days post pIpC treatment every other day for 5 days
• decreased in number and increased fraction of apoptotic in pIpC-treated mice
• at 21 days post pIpC treatment every other day for 5 days
• in peripheral blood following pIpC treatment
• in peripheral blood following pIpC treatment
• in peripheral blood following pIpC treatment
• in peripheral blood but not significantly depleted in the thymus
• in bone marrow and spleen at 21 days post pIpC treatment every other day for 5 days
• decrease in the number of T-lineage (CD3+) cells in bone marrow and spleen at 21 days post pIpC treatment every other day for 5 days
• following pIpC treatment
• decreased total number of multipotent progenitors following pIpC treatment
• percentage of cell death of hematopoietic stem cells and multipotent progenitors are similar to control
• at 21 days post pIpC treatment every other day for 5 days

immune system
• decreased myeloid cells in bone marrow and spleen at 21 days post pIpC treatment every other day for 5 days
• impact on myeloid compartment is more profound than B and T cell compartments
• in peripheral blood following pIpC treatment
• in peripheral blood following pIpC treatment
• in peripheral blood but not significantly depleted in the thymus
• in bone marrow and spleen at 21 days post pIpC treatment every other day for 5 days
• decrease in the number of T-lineage (CD3+) cells in bone marrow and spleen at 21 days post pIpC treatment every other day for 5 days
• at 21 days post pIpC treatment every other day for 5 days

cellular
• significantly increased fraction of cells in S and G2/M phases in bone marrow cells of 2 hours post pIpC-treated animals, with lesser increase in the myeloid progenitors
• in lethally irradiated host when transplanted with bone marrow cells





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory