About   Help   FAQ
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





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory