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Phenotypes Associated with This Genotype
Genotype
MGI:3842939
Allelic
Composition
Tg(Vav-BCL2)69Jad/0
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Vav-BCL2)69Jad mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die around 13 months of age

immune system
• the total number of B cells that undergo class switching is 50-fold higher than in wild-type mice
• 22 of 23 clones isolated from class-switching cells harbor on average about 6 somatic mutations compared to in wild-type cells where no mutations are found
• the ratio of CD4 cells per B cell is 25% to 50% lower than in wild-type mice
• 5-fold higher in the spleen at 18 weeks
• mice exhibit higher splenic T cell numbers than in wild-type and Tg(BCL2)22Wehi or Tg(BCL2)36Wehi mice
• the increase in CD4+ T cells is greater than the increase in CD8+ T cells
• the increase in CD4+ T cells is greater than the increase in CD8+ T cells
• mice exhibit a larger pool of cycling B cells with a germinal center phenotype than in wild-type mice
• however, expansion of germinal centers is dependent on CD4 T cell help
• at 18 weeks, mice exhibit an increased in germinal center size and number compared to in wild-type mice
• at 40 weeks, 15% to 25% of mice develop autoimmune glomerulonephritis

neoplasm
• 12% of mice develop plasma cell tumors
• less than 10% of mice develop lymphoblastic lymphomas
• in less than 10% of mice
• less than 10% of mice develop large cell B lymphomas (J:88565)
• diffuse large B cell lymphoma (J:228913)
• at 18 months, 37% to 50% of mice develop monoclonal follicular lymphoma (J:88565)
• in less than 10% of mice

renal/urinary system
• mice develop hypercellular glomeruli that contain amorphous, eosinophilic deposits
• most capillaries are no longer patent
• at 40 weeks, 15% to 25% of mice develop autoimmune glomerulonephritis
• Bowman epithelium proliferates to form crescents in the most advanced cases

endocrine/exocrine glands
• in less than 10% of mice

hematopoietic system
• the total number of B cells that undergo class switching is 50-fold higher than in wild-type mice
• 22 of 23 clones isolated from class-switching cells harbor on average about 6 somatic mutations compared to in wild-type cells where no mutations are found
• the ratio of CD4 cells per B cell is 25% to 50% lower than in wild-type mice
• 5-fold higher in the spleen at 18 weeks
• mice exhibit higher splenic T cell numbers than in wild-type and Tg(BCL2)22Wehi or Tg(BCL2)36Wehi mice
• the increase in CD4+ T cells is greater than the increase in CD8+ T cells
• the increase in CD4+ T cells is greater than the increase in CD8+ T cells
• mice exhibit a larger pool of cycling B cells with a germinal center phenotype than in wild-type mice
• however, expansion of germinal centers is dependent on CD4 T cell help
• at 18 weeks, mice exhibit an increased in germinal center size and number compared to in wild-type mice

cardiovascular system
• most capillaries are no longer patent

growth/size/body

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
follicular lymphoma DOID:0050873 OMIM:151430
J:88565


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
04/30/2024
MGI 6.23
The Jackson Laboratory