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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Actbtm4(cre/ERT2)Npa
targeted mutation 4, Novartis Pharma AG
MGI:5514361
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Actbtm4(cre/ERT2)Npa/Actb+
Sgpl1tm1.1Npa/Sgpl1tm1.1Npa
involves: BALB/cJ * C57BL/6 MGI:5515215


Genotype
MGI:5515215
cn1
Allelic
Composition
Actbtm4(cre/ERT2)Npa/Actb+
Sgpl1tm1.1Npa/Sgpl1tm1.1Npa
Genetic
Background
involves: BALB/cJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Actbtm4(cre/ERT2)Npa mutation (0 available); any Actb mutation (51 available)
Sgpl1tm1.1Npa mutation (0 available); any Sgpl1 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• with tamoxifen treatment mice show normal survival up to 6 months of observation

growth/size/body
N
• after tamoxifen treatment mice show normal weight gain up to 6 months of observation

hematopoietic system
• thymocytes are enriched in mature single-positive T cells
• with tamoxifen treatment total numbers are decreased significantly, with no significant change in germinal center B cells
• with tamoxifen treatment total numbers are decreased significantly, with no significant change in germinal center B cells
• with tamoxifen treatment numbers of CD4+Foxp3+ T cells are reduced 3-4 fold in spleen and increased more than 4-fold in lymph nodes with tamoxifen treatment
• mice treated with tamoxifen daily for 5 days have decreases in CD4- and CD8-positive T cells by up to 85% two weeks later, lasting for at least 6 months; CD19-positive B cell numbers are unchanged
• at 8 weeks after tamoxifen treatment, splenic populations of CD4- and CD8-positive T cells are sharply reduced
• at 8 weeks after tamoxifen treatment splenic cellularity sharply decreased with significant reductions in CD- and CD8-positive T cells and subpopulations of B cells

immune system
• thymocytes are enriched in mature single-positive T cells
• with tamoxifen treatment total numbers are decreased significantly, with no significant change in germinal center B cells
• with tamoxifen treatment total numbers are decreased significantly, with no significant change in germinal center B cells
• with tamoxifen treatment numbers of CD4+Foxp3+ T cells are reduced 3-4 fold in spleen and increased more than 4-fold in lymph nodes with tamoxifen treatment
• mice treated with tamoxifen daily for 5 days have decreases in CD4- and CD8-positive T cells by up to 85% two weeks later, lasting for at least 6 months; CD19-positive B cell numbers are unchanged
• at 8 weeks after tamoxifen treatment, splenic populations of CD4- and CD8-positive T cells are sharply reduced
• at 8 weeks after tamoxifen treatment splenic cellularity sharply decreased with significant reductions in CD- and CD8-positive T cells and subpopulations of B cells
• with tamoxifen treatment lymph node cell numbers are significantly increased with an increase in CD4- and CD8-positive T cells and total B cell numbers (except germinal center B cells
• tamoxifen treated mice are protected from delayed-type hypersensitivity reaction induced by localized challenge with sheep red blood cells
• tamoxifen treated mice are almost completely protected from MOG-induced EAE

homeostasis/metabolism
• 2 weeks after induction of cre, levels of S1P (Sgpl1 substrate) are increased 4-fold (heart) to 100-fold (spleen/lymph nodes) with no significant increase in the brain or spinal cord; blood concentrations are elevate only 1.6-fold
• ceramide (S1P precursor) is not significantly elevated with Sph (S1P precursor) increased 16-fold
• increase of sphingolipid metabolites is much less pronounce than in constitutive Sgpl1 knockouts

endocrine/exocrine glands
• thymocytes are enriched in mature single-positive T cells





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory