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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gt(ROSA)26Sortm11(Lmp1)Rsky
targeted mutation 11, Klaus Rajewsky
MGI:5314030
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+ involves: C57BL/6 MGI:5314101
cn2
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+
Tcrbtm1Mom/Tcrb+
Tcrdtm1Mom/Tcrdtm1Mom
Cd19tm1(cre)Cgn/Cd19+
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 MGI:5314091
cn3
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+
Tcrbtm1Mom/Tcrbtm1Mom
Tcrdtm1Mom/Tcrdtm1Mom
Cd19tm1(cre)Cgn/Cd19+
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 MGI:5314096
cn4
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+
Klrk1tm1Dhr/Klrk1tm1Dhr
Cd19tm1(cre)Cgn/Cd19+
involves: 129P2/OlaHsd * C57BL/6 MGI:5314087
cn5
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+
Cd19tm1(cre)Cgn/Cd19+
involves: 129P2/OlaHsd * C57BL/6 MGI:5314104
cn6
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+
Cd19tm1(cre/ERT2)Rsky/Cd19+
involves: 129P2/OlaHsd * C57BL/6J MGI:5614487


Genotype
MGI:5314101
cn1
Allelic
Composition
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm11(Lmp1)Rsky mutation (0 available); any Gt(ROSA)26Sor mutation (993 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• B cells treated with TAT-cre proliferate in culture unlike wild-type cells
• B cells treated with TAT-cre exhibit increased cell size compared with wild-type cells

hematopoietic system
• B cells treated with TAT-cre proliferate in culture unlike wild-type cells
• B cells treated with TAT-cre exhibit increased cell size compared with wild-type cells

cellular
• B cells treated with TAT-cre proliferate in culture unlike wild-type cells




Genotype
MGI:5314091
cn2
Allelic
Composition
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+
Tcrbtm1Mom/Tcrb+
Tcrdtm1Mom/Tcrdtm1Mom
Cd19tm1(cre)Cgn/Cd19+
Genetic
Background
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cd19tm1(cre)Cgn mutation (11 available); any Cd19 mutation (60 available)
Gt(ROSA)26Sortm11(Lmp1)Rsky mutation (0 available); any Gt(ROSA)26Sor mutation (993 available)
Tcrbtm1Mom mutation (12 available); any Tcrb mutation (97 available)
Tcrdtm1Mom mutation (13 available); any Tcrd mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

immune system

hematopoietic system

growth/size/body




Genotype
MGI:5314096
cn3
Allelic
Composition
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+
Tcrbtm1Mom/Tcrbtm1Mom
Tcrdtm1Mom/Tcrdtm1Mom
Cd19tm1(cre)Cgn/Cd19+
Genetic
Background
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cd19tm1(cre)Cgn mutation (11 available); any Cd19 mutation (60 available)
Gt(ROSA)26Sortm11(Lmp1)Rsky mutation (0 available); any Gt(ROSA)26Sor mutation (993 available)
Tcrbtm1Mom mutation (12 available); any Tcrb mutation (97 available)
Tcrdtm1Mom mutation (13 available); any Tcrd mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

immune system

liver/biliary system
• occasionally

neoplasm
• most tumors resemble diffuse large B cell lymphomas (in 6 of 9 mice)

hematopoietic system

growth/size/body
• occasionally




Genotype
MGI:5314087
cn4
Allelic
Composition
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+
Klrk1tm1Dhr/Klrk1tm1Dhr
Cd19tm1(cre)Cgn/Cd19+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cd19tm1(cre)Cgn mutation (11 available); any Cd19 mutation (60 available)
Gt(ROSA)26Sortm11(Lmp1)Rsky mutation (0 available); any Gt(ROSA)26Sor mutation (993 available)
Klrk1tm1Dhr mutation (3 available); any Klrk1 mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
N
• mice are protected from Lmp1-driven lymphomagenesis




Genotype
MGI:5314104
cn5
Allelic
Composition
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+
Cd19tm1(cre)Cgn/Cd19+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cd19tm1(cre)Cgn mutation (11 available); any Cd19 mutation (60 available)
Gt(ROSA)26Sortm11(Lmp1)Rsky mutation (0 available); any Gt(ROSA)26Sor mutation (993 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 2 weeks after treatment with a cocktail of depleting antibodies (anti-CD4, anti-CD8 and anti-Thy1)

immune system
• 2 weeks after treatment with a cocktail of depleting antibodies (anti-CD4, anti-CD8 and anti-Thy1)
• impaired in the bone marrow
• at 6 to 12 weeks in the bone marrow
• at 6 to 12 weeks in the spleen and bone marrow
• absent CD19+Fas+ B cells at 8 to 11 weeks in the spleen
• at 6 to 12 weeks in the bone marrow
• at 6 to 12 weeks in the bone marrow
• at P8, mice exhibit an increase in CD19+ B cells in the spleen compared with control mice
• at P8, but not P3, in the spleen
• of activated T cells in the bone marrow at 6 to 12 weeks
• at P8, but not P3, in the spleen
• of activated T cells in the bone marrow at 6 to 12 weeks
• after 2 weeks, mice treated with a cocktail of depleting antibodies (anti-CD4, anti-CD8 and anti-Thy1) exhibit splenomegaly and become terminally ill unlike control mice
• after 2 weeks, mice treated with a cocktail of depleting antibodies (anti-CD4, anti-CD8 and anti-Thy1) exhibit rapid expansion of Lmp1+ B cell blasts largely confined to peripheral lymphoid organs and the bone marrow with some infiltration into the liver and rarely into lungs and kidneys compared with control mice
• however, mice treated with one depleting antibodies (anti-CD4, anti-CD8, anti-Thy1 or anti-CD4 and anti-CD8) do not exhibit expansion of B cells
• in an in vitro tumor killing assay, CD4+ T cells exhibit reduced tumor killing compared with control cells
• however, CD4+ T cells exhibit normal prevention of tumor outgrowth in vivo and elimination of nontransformed L,p1+ B cells upon transfer
• the CD8+ compartment of the bone marrow of mice treated with a cocktail of depleting antibodies (anti-CD4, anti-CD8 and anti-Thy1) exhibit a 2-fold increase in cells expressing IFN-gamma, TNF-alpha, IL4 and IL17
• in vivo, CD8+ T cells exhibit reduced prevention of tumor outgrowth compared with control cells
• however, CD8+ T cell exhibit normal tumor killing in vitro and elimination of nontransformed L,p1+ B cells upon transfer
• minor in T cells co-cultured with tumor or B cells
• minor in T cells co-cultured with tumor or B cells

hematopoietic system
• after 2 weeks, mice treated with a cocktail of depleting antibodies (anti-CD4, anti-CD8 and anti-Thy1) exhibit rapid expansion of Lmp1+ B cell blasts largely confined to peripheral lymphoid organs and the bone marrow with some infiltration into the liver and rarely into lungs and kidneys compared with control mice
• however, mice treated with one depleting antibodies (anti-CD4, anti-CD8, anti-Thy1 or anti-CD4 and anti-CD8) do not exhibit expansion of B cells
• 2 weeks after treatment with a cocktail of depleting antibodies (anti-CD4, anti-CD8 and anti-Thy1)
• impaired in the bone marrow
• at 6 to 12 weeks in the bone marrow
• at 6 to 12 weeks in the spleen and bone marrow
• absent CD19+Fas+ B cells at 8 to 11 weeks in the spleen
• at 6 to 12 weeks in the bone marrow
• at 6 to 12 weeks in the bone marrow
• at P8, mice exhibit an increase in CD19+ B cells in the spleen compared with control mice
• at P8, but not P3, in the spleen
• of activated T cells in the bone marrow at 6 to 12 weeks
• at P8, but not P3, in the spleen
• of activated T cells in the bone marrow at 6 to 12 weeks
• in an in vitro tumor killing assay, CD4+ T cells exhibit reduced tumor killing compared with control cells
• however, CD4+ T cells exhibit normal prevention of tumor outgrowth in vivo and elimination of nontransformed L,p1+ B cells upon transfer
• the CD8+ compartment of the bone marrow of mice treated with a cocktail of depleting antibodies (anti-CD4, anti-CD8 and anti-Thy1) exhibit a 2-fold increase in cells expressing IFN-gamma, TNF-alpha, IL4 and IL17
• in vivo, CD8+ T cells exhibit reduced prevention of tumor outgrowth compared with control cells
• however, CD8+ T cell exhibit normal tumor killing in vitro and elimination of nontransformed L,p1+ B cells upon transfer

growth/size/body
• 2 weeks after treatment with a cocktail of depleting antibodies (anti-CD4, anti-CD8 and anti-Thy1)

cellular
• after 2 weeks, mice treated with a cocktail of depleting antibodies (anti-CD4, anti-CD8 and anti-Thy1) exhibit rapid expansion of Lmp1+ B cell blasts largely confined to peripheral lymphoid organs and the bone marrow with some infiltration into the liver and rarely into lungs and kidneys compared with control mice
• however, mice treated with one depleting antibodies (anti-CD4, anti-CD8, anti-Thy1 or anti-CD4 and anti-CD8) do not exhibit expansion of B cells




Genotype
MGI:5614487
cn6
Allelic
Composition
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+
Cd19tm1(cre/ERT2)Rsky/Cd19+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cd19tm1(cre/ERT2)Rsky mutation (1 available); any Cd19 mutation (60 available)
Gt(ROSA)26Sortm11(Lmp1)Rsky mutation (0 available); any Gt(ROSA)26Sor mutation (993 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• with B cell blasts outnumbering normal splenic B cells 20-fold in tamoxifen-treated mice
• CD19+ B cells in tamoxifen-treated mice
• B cell blasts outnumbering normal splenic B cells 20-fold in tamoxifen-treated mice
• however, cell counts return to baseline after 2 weeks and a second application of tamoxifen does not result in another wave of B cell expansion
• massive expansion in tamoxifen-treated mice
• massive expansion in tamoxifen-treated mice
• in tamoxifen-treated mice
• however, T cell numbers decrease 8 days after tamoxifen application
• vigorous degranulation when T cells from tamoxifen-treated mice are exposed to LMP1-transduced B cells in vitro

hematopoietic system
• with B cell blasts outnumbering normal splenic B cells 20-fold in tamoxifen-treated mice
• CD19+ B cells in tamoxifen-treated mice
• B cell blasts outnumbering normal splenic B cells 20-fold in tamoxifen-treated mice
• however, cell counts return to baseline after 2 weeks and a second application of tamoxifen does not result in another wave of B cell expansion
• massive expansion in tamoxifen-treated mice
• massive expansion in tamoxifen-treated mice
• in tamoxifen-treated mice
• however, T cell numbers decrease 8 days after tamoxifen application
• vigorous degranulation when T cells from tamoxifen-treated mice are exposed to LMP1-transduced B cells in vitro

growth/size/body
• with B cell blasts outnumbering normal splenic B cells 20-fold in tamoxifen-treated mice





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory