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Phenotypes Associated with This Genotype
Genotype
MGI:2664241
Allelic
Composition
Mybl1tm1Epr/Mybl1tm1Epr
Genetic
Background
involves: 129 * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mybl1tm1Epr mutation (1 available); any Mybl1 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• ~2-fold reduction in percentage of splenic B cells (B220+) relative to wild-type controls; however, proportions of splenic immature and mature B cells are normal
• normal B cell development in the bone marrow, as shown by normal numbers of pro-B, pre-B, immature, and mature B cell subpopulations
• expanded red pulp areas
• reduced average spleen size
• mild splenic hypoplasia involving all areas of the white pulp
• the number of "spontaneous" GCs in naive mutant spleens is severalfold lower than that in wild-type controls
• impaired primary serum antibody response, following immunization with the T cell-dependent antigen NP-CGG in alum, as shown by reduced primary serum levels of IgG3 and IgG1 (the major isotypes in this response), as well as IgG2a; however, the early primary IgM response and secondary anti-NP serum Ab responses are normal
• normal germinal center reaction following immunization with the T cell-dependent antigen NP-CGG
• normal development of B cell memory, as shown by normal V gene somatic hypermutation and Ag affinity-based positive selection during the anti-NP response
• normal rate of B cell proliferation following in vitro stimulation with LPS, anti-CD40, or anti-IgM
• normal H chain class switching by B cells following in vitro stimulation with LPS or LPS and IL-4
• reduced primary serum levels of IgG1 following immunization with the T cell-dependent antigen NP-CGG
• reduced primary serum levels of IgG2a following immunization with the T cell-dependent antigen NP-CGG
• reduced primary serum levels of IgG3 following immunization with the T cell-dependent antigen NP-CGG

hematopoietic system
• ~2-fold reduction in percentage of splenic B cells (B220+) relative to wild-type controls; however, proportions of splenic immature and mature B cells are normal
• normal B cell development in the bone marrow, as shown by normal numbers of pro-B, pre-B, immature, and mature B cell subpopulations
• expanded red pulp areas
• reduced average spleen size
• mild splenic hypoplasia involving all areas of the white pulp
• the number of "spontaneous" GCs in naive mutant spleens is severalfold lower than that in wild-type controls
• reduced primary serum levels of IgG1 following immunization with the T cell-dependent antigen NP-CGG
• reduced primary serum levels of IgG2a following immunization with the T cell-dependent antigen NP-CGG
• reduced primary serum levels of IgG3 following immunization with the T cell-dependent antigen NP-CGG


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)
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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory