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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ighmtm1(Bcl6)Rdf
targeted mutation 1, Riccardo Dalla-Favera
MGI:3581517
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Atmintm1.1Jhh/Atmintm1.1Jhh
Ighmtm1(Bcl6)Rdf/Ighm+
Tg(Fcer2a-cre)5Mbu/0
B6.Cg-Atmintm1.1Jhh Ighmtm1(Bcl6)Rdf Tg(Fcer2a-cre)5Mbu MGI:5755471
cx2
Bcl6tm2Rdf/Bcl6tm2Rdf
Ighmtm1(Bcl6)Rdf/?
involves: 129/Sv * 129S1/Sv * C57BL/6 MGI:3582785
ot3
Ighmtm1(Bcl6)Rdf/? involves: 129/Sv * C57BL/6 MGI:3582784


Genotype
MGI:5755471
cn1
Allelic
Composition
Atmintm1.1Jhh/Atmintm1.1Jhh
Ighmtm1(Bcl6)Rdf/Ighm+
Tg(Fcer2a-cre)5Mbu/0
Genetic
Background
B6.Cg-Atmintm1.1Jhh Ighmtm1(Bcl6)Rdf Tg(Fcer2a-cre)5Mbu
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atmintm1.1Jhh mutation (2 available); any Atmin mutation (38 available)
Ighmtm1(Bcl6)Rdf mutation (1 available); any Ighm mutation (55 available)
Tg(Fcer2a-cre)5Mbu mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• mice exhibit similar tumorigenesis as Atmintm1.1Jhh/Atmintm1.1Jhh Tg(Fcer2a-cre)5Mbu mice




Genotype
MGI:3582785
cx2
Allelic
Composition
Bcl6tm2Rdf/Bcl6tm2Rdf
Ighmtm1(Bcl6)Rdf/?
Genetic
Background
involves: 129/Sv * 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bcl6tm2Rdf mutation (0 available); any Bcl6 mutation (55 available)
Ighmtm1(Bcl6)Rdf mutation (1 available); any Ighm mutation (55 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• Igh-6tm1(Bcl6)Rdf was unable to rescue the inflammatory phenotype observed in homozygous Bcl6 null mice
• although proliferation of B cells expressing germinal center markers was induced, the cells did not aggregate in typical germinal center structures

hematopoietic system
• although proliferation of B cells expressing germinal center markers was induced, the cells did not aggregate in typical germinal center structures




Genotype
MGI:3582784
ot3
Allelic
Composition
Ighmtm1(Bcl6)Rdf/?
Genetic
Background
involves: 129/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ighmtm1(Bcl6)Rdf mutation (1 available); any Ighm mutation (55 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• showed increased mortality at about 13 months of age and only about 80% survived at 15 months

immune system
• 42% exhibited abnormal B cell expansions involving predominately the spleen but also the lymph nodes compared to 11% in wild-type and displayed features of benign lymphoproliferative disease
• about a 30% reduction in the number of total plasmacytoid cells (B220+/- CD138+), mainly due to a decrease in post-CSR plasma cells (IgM-IgD-), while IgM+IgD+ plasma cells were normal
• 17% displayed a complete effacement of the splenic lymphoid architecture due to the proliferation of large lymphoid cells
• 17% exhibited a modest splenomegaly at 6 months of age
• partial effacement of the follicular architecture with the appearance of blast cells
• nonimmunized mutant mice displayed an increased number of germinal centers, comparable to that observed upon immunization in wild-type mice, and the increase in the number of germinal centers and an increase in the total germinal center area persisted after immunization
• expanded white pulp composed predominately of B cells, but also included disorganized accumulations of other cell types such as T cells and dendritic cells
• displayed a small (20-50%) reduction in total serum immunoglobulin levels of all subclasses, except for IgM, both under basal conditions and after immunization with T-dependent antigens

neoplasm
• between 15 and 20 months, 36-62% developed clonal B cell lymphomas, predominately of splenic orgin, with or without nodal involvement
• tumors displayed a mature B cell phenotype and most were histologically reminiscent of human diffuse large B cell lymphomas and contained clonal karyotypic aberrations

hematopoietic system
• 42% exhibited abnormal B cell expansions involving predominately the spleen but also the lymph nodes compared to 11% in wild-type and displayed features of benign lymphoproliferative disease
• about a 30% reduction in the number of total plasmacytoid cells (B220+/- CD138+), mainly due to a decrease in post-CSR plasma cells (IgM-IgD-), while IgM+IgD+ plasma cells were normal
• 17% displayed a complete effacement of the splenic lymphoid architecture due to the proliferation of large lymphoid cells
• 17% exhibited a modest splenomegaly at 6 months of age
• partial effacement of the follicular architecture with the appearance of blast cells
• nonimmunized mutant mice displayed an increased number of germinal centers, comparable to that observed upon immunization in wild-type mice, and the increase in the number of germinal centers and an increase in the total germinal center area persisted after immunization
• expanded white pulp composed predominately of B cells, but also included disorganized accumulations of other cell types such as T cells and dendritic cells
• displayed a small (20-50%) reduction in total serum immunoglobulin levels of all subclasses, except for IgM, both under basal conditions and after immunization with T-dependent antigens

growth/size/body
• 17% exhibited a modest splenomegaly at 6 months of age

cellular
• 42% exhibited abnormal B cell expansions involving predominately the spleen but also the lymph nodes compared to 11% in wild-type and displayed features of benign lymphoproliferative disease

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
non-Hodgkin lymphoma DOID:0060060 OMIM:605027
J:98937





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