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Phenotypes Associated with This Genotype
Genotype
MGI:3759780
Allelic
Composition
Il2tm1Hor/Il2tm1Hor
Tg(DO11.10)10Dlo/?
Genetic
Background
C.Cg-Il2tm1Hor Tg(DO11.10)10Dlo
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Il2tm1Hor mutation (5 available); any Il2 mutation (32 available)
Tg(DO11.10)10Dlo mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• the mean survival time is 4 months, which is significantly shorter than the average life expectancy of BALB/C mic
• however, the mean survival time is much longer than Il2 null mice on a BALB/c background that do not carry the TCR transgene

immune system
• when transferred into athymic mice, CD4 T cells continue to proliferate for up to three weeks in response to antigen
• CD 4 T cells from these transfer experiments also express high levels of activation markers
• However, when transferred with wild-type CD4-postive CD25-positive T cells, the mutant CD4 T cells stop proliferating between one to two weeks after antigen encounter
• when transferred into athymic mice, there are 10-100 fold higher numbers of activated T cells three weeks after antigen
• the abnormal proliferation of CD4 T cells upon transfer into athymic mice is reduced by the addition of wild-type CD4-postive CD25-positive T cells
• this suggests there is a defect in the regulatory T cell population in these mice

hematopoietic system
• when transferred into athymic mice, CD4 T cells continue to proliferate for up to three weeks in response to antigen
• CD 4 T cells from these transfer experiments also express high levels of activation markers
• However, when transferred with wild-type CD4-postive CD25-positive T cells, the mutant CD4 T cells stop proliferating between one to two weeks after antigen encounter
• when transferred into athymic mice, there are 10-100 fold higher numbers of activated T cells three weeks after antigen
• the abnormal proliferation of CD4 T cells upon transfer into athymic mice is reduced by the addition of wild-type CD4-postive CD25-positive T cells
• this suggests there is a defect in the regulatory T cell population in these mice

cellular
• when transferred into athymic mice, CD4 T cells continue to proliferate for up to three weeks in response to antigen
• CD 4 T cells from these transfer experiments also express high levels of activation markers
• However, when transferred with wild-type CD4-postive CD25-positive T cells, the mutant CD4 T cells stop proliferating between one to two weeks after antigen encounter


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
01/06/2026
MGI 6.24
The Jackson Laboratory