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Phenotypes Associated with This Genotype
Genotype
MGI:3603014
Allelic
Composition
Myctm1Lbox/Myctm1Lbox
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myctm1Lbox mutation (0 available); any Myc mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Histopathological analysis of lymphomas in Myctm1Lbox/Myctm1Lbox and Myctm1Lbox/Myc+ mice

mortality/aging
• mean age of death is about 314 days

immune system
• increased apoptosis of B cells from young homozygotes is seen in culture without activating stimuli; however, B cells from lymphomas remain viable in culture for longer periods of time compared to wild-type cells
• antigen-stimulated B cell proliferation is increased about 2-fold compared to wild-type mice and the number of B cells in S and G2/M phase is increased to 47% compared to 24% of wild-type B cells
• around 10 months of age, a profound enlargement of the spleen is seen
• around 10 months of age, a 5-12 fold increase in spleen weight is seen
• in young (6 weeks-3months) mutants, the percentage of B cells in the spleen is increased with a 7-10 fold increase in the B220+IgM+IgDlow cell population and a slight increase in the B220+IgM+ cell population is seen in the bone marrow
• in young (6 weeks-3months) mutants, the percentage of T cells in the spleen is decreased; however T cell development in the thymus is normal and the ratio of CD4 and CD8 cells is similar to wild-type
• around 10 months of age profound enlargement of the lymph nodes is seen

neoplasm
• B cell derived lymphomas with diffuse infiltration in the spleen and lymph nodes, varying degrees of infiltration into the lung, kidney, and intestine, and a 'starry sky' appearance characteristic of Burkitt's lymphoma are seen

hematopoietic system
• increased apoptosis of B cells from young homozygotes is seen in culture without activating stimuli; however, B cells from lymphomas remain viable in culture for longer periods of time compared to wild-type cells
• antigen-stimulated B cell proliferation is increased about 2-fold compared to wild-type mice and the number of B cells in S and G2/M phase is increased to 47% compared to 24% of wild-type B cells
• around 10 months of age, a profound enlargement of the spleen is seen
• around 10 months of age, a 5-12 fold increase in spleen weight is seen
• in young (6 weeks-3months) mutants, the percentage of B cells in the spleen is increased with a 7-10 fold increase in the B220+IgM+IgDlow cell population and a slight increase in the B220+IgM+ cell population is seen in the bone marrow
• in young (6 weeks-3months) mutants, the percentage of T cells in the spleen is decreased; however T cell development in the thymus is normal and the ratio of CD4 and CD8 cells is similar to wild-type

cellular
• increased apoptosis of B cells from young homozygotes is seen in culture without activating stimuli; however, B cells from lymphomas remain viable in culture for longer periods of time compared to wild-type cells
• antigen-stimulated B cell proliferation is increased about 2-fold compared to wild-type mice and the number of B cells in S and G2/M phase is increased to 47% compared to 24% of wild-type B cells

growth/size/body
• around 10 months of age, a profound enlargement of the spleen is seen
• around 10 months of age, a 5-12 fold increase in spleen weight is seen

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Burkitt lymphoma DOID:8584 OMIM:113970
J:97900


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
12/10/2024
MGI 6.24
The Jackson Laboratory