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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Bcl6tm1Rdf
targeted mutation 1, Riccardo Dalla-Favera
MGI:2158437
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Bcl6tm1Rdf/Bcl6tm1Rdf involves: 129S1/Sv MGI:3582781


Genotype
MGI:3582781
hm1
Allelic
Composition
Bcl6tm1Rdf/Bcl6tm1Rdf
Genetic
Background
involves: 129S1/Sv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bcl6tm1Rdf mutation (0 available); any Bcl6 mutation (55 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• 51.7% the weight of wild-type at 6 months of age
• some mice exhibited hyperplasia due to infiltration by non-lymphoid cells and occasional hypoplasia in very young mice

immune system
• smaller in some mice, particularly in those with early infections
• some mice exhibited hyperplasia due to infiltration by non-lymphoid cells and occasional hypoplasia in very young mice
• bone marrow showed a modest increase in eosinophilic precursors
• no germinal centers in the spleen of non-immunized mice or in mice immunized with T-dependent antigen
• failed to form a germinal center upon immunization with the T-dependent antigen
• failed to form a germinal center in the lymph nodes upon immunization with the T-dependent antigen
• increase in IgG- and IgE-bearing B cells
• 4-20-fold reduction for all IgG subtypes compared to wild-type when immunized with the T-cell dependent antigen
• 2-fold reduction compared to wild-type when immunized with the T-cell dependent antigen
• defect in T-cell-dependent antibody responses resulting in the development of a Th2-type inflammatory disease
• reduced T-cell-dependent antibody response of most Ig isotypes
• complete lack of affinity maturation
• develop a Th2-type inflammatory disease involving multiple organs including the myocardium, spleen, gut, liver, lacrimal gland and skin, characterized by infiltrations of eosinophils and IgE-bearing B lymphocytes
• presence of eosinophilic infiltrates in the heart
• presence of eosinophilic infiltrates in lung, heart and mediastinal lymph nodes that was associated with acidophilic macrophage pneumonia (characterized by the infiltration of macrophages filled by degradation products of eosinophils)
• about half displayed infections within the first 3 months of life, most frequently involving the oesophagus as well as other mucosal sites in the upper respiratory and digestive tracts and the lung

hematopoietic system
• smaller in some mice, particularly in those with early infections
• some mice exhibited hyperplasia due to infiltration by non-lymphoid cells and occasional hypoplasia in very young mice
• bone marrow showed a modest increase in eosinophilic precursors
• no germinal centers in the spleen of non-immunized mice or in mice immunized with T-dependent antigen
• increase in IgG- and IgE-bearing B cells
• 4-20-fold reduction for all IgG subtypes compared to wild-type when immunized with the T-cell dependent antigen
• 2-fold reduction compared to wild-type when immunized with the T-cell dependent antigen
• defect in T-cell-dependent antibody responses resulting in the development of a Th2-type inflammatory disease

respiratory system
• presence of eosinophilic infiltrates in lung, heart and mediastinal lymph nodes that was associated with acidophilic macrophage pneumonia (characterized by the infiltration of macrophages filled by degradation products of eosinophils)

cardiovascular system
• presence of eosinophilic infiltrates in the heart

liver/biliary system

endocrine/exocrine glands
• smaller in some mice, particularly in those with early infections





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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
07/05/2024
MGI 6.24
The Jackson Laboratory