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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Flt3ltm1Imx
targeted mutation 1, Immunex Corporation
MGI:2158499
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Flt3ltm1Imx/Flt3ltm1Imx C57BL/6-Flt3ltm1Imx MGI:3656072
hm2
Flt3ltm1Imx/Flt3ltm1Imx involves: C57BL/6 MGI:5444882


Genotype
MGI:3656072
hm1
Allelic
Composition
Flt3ltm1Imx/Flt3ltm1Imx
Genetic
Background
C57BL/6-Flt3ltm1Imx
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Flt3ltm1Imx mutation (1 available); any Flt3l mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• other immune globulins and cell surface IgM are all normal
• reduced numbers of immature myeloid cells in bone marrow
• 75-90% reduction in B cell precursor cells, both frequency and absolute numbers (J:62536)
• preferentially reduced in number (J:79569)
• neutrophiles increased by about 20%
• WBC reduced 45% in peripheral blood
• lymphoid related dendritic cells are reduced in the spleen, thymus, and lymph nodes (J:62536)
• reduced in numbers in parenchymal organs such as the heart but not in skin (J:89868)
• less extensive dendrites on all dendritic cells (J:89868)
• proportion of lymphocytes reduced significantly by about 76%
• pro-T cells are reduced up to 72% in the thymus whereas more mature pre-T cells are present in more normal numbers
• slight but significant reduction in peripheral B cell numbers
• preferentially reduced in number
• numbers of natural killer cells in the spleen are dramatically reduced
• myeloid related dendritic cells reduced in spleen, thymus, and lymph nodes (J:62536)
• reduced in numbers in parenchymal organs such as the heart but not in skin (J:89868)
• less extensive dendrites on all dendritic cells (J:89868)
• reduced by 30%
• both T and B cell numbers are reduced but the ratio of T to B cells is unchanged
• organ architecture remains normal
• reduced by 35%
• both T and B cell numbers are reduced but the ratio of T to B cells is unchanged
• organ architecture remains normal
• allographs of hearts to BALB/c recipients show prolonged survival but not skin grafts

hematopoietic system
• reduced absolute number of myeloid lineage precursors in bone marrow
• reduced numbers of immature myeloid cells in bone marrow
• cellularity reduced by 27%
• earliest common lymphoid cell precursors in bone marrow are reduced 10 fold
• multipotent precursors reduced by 39% in bone marrow
• 75-90% reduction in B cell precursor cells, both frequency and absolute numbers (J:62536)
• preferentially reduced in number (J:79569)
• neutrophiles increased by about 20%
• WBC reduced 45% in peripheral blood
• lymphoid related dendritic cells are reduced in the spleen, thymus, and lymph nodes (J:62536)
• reduced in numbers in parenchymal organs such as the heart but not in skin (J:89868)
• less extensive dendrites on all dendritic cells (J:89868)
• proportion of lymphocytes reduced significantly by about 76%
• pro-T cells are reduced up to 72% in the thymus whereas more mature pre-T cells are present in more normal numbers
• slight but significant reduction in peripheral B cell numbers
• preferentially reduced in number
• numbers of natural killer cells in the spleen are dramatically reduced
• myeloid related dendritic cells reduced in spleen, thymus, and lymph nodes (J:62536)
• reduced in numbers in parenchymal organs such as the heart but not in skin (J:89868)
• less extensive dendrites on all dendritic cells (J:89868)
• reduced by 30%
• both T and B cell numbers are reduced but the ratio of T to B cells is unchanged
• organ architecture remains normal
• other immune globulins and cell surface IgM are all normal




Genotype
MGI:5444882
hm2
Allelic
Composition
Flt3ltm1Imx/Flt3ltm1Imx
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Flt3ltm1Imx mutation (1 available); any Flt3l mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• CD11bhi dendritic cells do not migrate to mediastinal lymph nodes following LPS instillation

immune system
• CD11bhi dendritic cells do not migrate to mediastinal lymph nodes following LPS instillation
• diphtheria toxin-treated mice exhibit increased numbers of splenic Ly6G+ neutrophils compared with controls
• diphtheria toxin-treated mice exhibit complete ablation of all CD11chiMHCII+ dendritic cells regardless of pre-dendritic cell or monocyte origin
• reduced Lin-CD11chi classical dendritic cells in diphtheria-treated T. gondii-infected bone marrow chimeras
• mice lack CD103+ dendritic cells in the lungs in steady state conditions and following OVA/LPS instillation
• lungs contain a slightly reduced number of CD11bhi dendritic cells as compared to wild-type
• CD11bhi dendritic cells are comprised mostly of the CD14hi subset with few CD14med/lo cells
• mediastinal lymph nodes lack CD11bhi dendritic cells following LPS instillation
• in diphtheria toxin-treated mice
• in diphtheria toxin-treated mice
• in the splenic red pulp of diphtheria toxin treated bone marrow chimeras
• F4/80+ red pulp macrophage are absent in diphtheria toxin-treated mice
• CD169+ marginal zone macrophages are almost absent in the spleen of diphtheria toxin-treated mice
• lymph node subscapular sinus macrophages are reduced in diphtheria toxin-treated mice
• however, F4/80+ medullar macrophages in the skin lymph nodes are unaffected in diphtheria toxin-treated mice
• in diphtheria toxin-treated mice
• reduced IFNgamma+ CD3+CD4+ T cells in diphtheria toxin-treated bone marrow chimeras immunized with either alpha-DEC-205-GAGp24 or alpha-Treml4-GAGp24, or infected with T. gondii
• diphtheria toxin-treated bone marrow chimeras exhibit fail to exhibit an antitumor memory response unlike control mice and Zbtb46tm1(HBEGF)Mnz heterozygotes
• TH2, but not TH1, induction by dendritic cells is impaired
• diphtheria toxin-treated mice infected with T. gondii exhibit decreased IFNgamma+ CD3+CD4+ T cells and increased parasitic burden compared with controls and Zbtb46tm1(HBEGF)Mnz heterozygotes

hematopoietic system
• CD11bhi dendritic cells do not migrate to mediastinal lymph nodes following LPS instillation
• diphtheria toxin-treated mice exhibit increased numbers of splenic Ly6G+ neutrophils compared with controls
• diphtheria toxin-treated mice exhibit complete ablation of all CD11chiMHCII+ dendritic cells regardless of pre-dendritic cell or monocyte origin
• reduced Lin-CD11chi classical dendritic cells in diphtheria-treated T. gondii-infected bone marrow chimeras
• mice lack CD103+ dendritic cells in the lungs in steady state conditions and following OVA/LPS instillation
• lungs contain a slightly reduced number of CD11bhi dendritic cells as compared to wild-type
• CD11bhi dendritic cells are comprised mostly of the CD14hi subset with few CD14med/lo cells
• mediastinal lymph nodes lack CD11bhi dendritic cells following LPS instillation
• in diphtheria toxin-treated mice
• in diphtheria toxin-treated mice
• in the splenic red pulp of diphtheria toxin treated bone marrow chimeras
• F4/80+ red pulp macrophage are absent in diphtheria toxin-treated mice
• CD169+ marginal zone macrophages are almost absent in the spleen of diphtheria toxin-treated mice
• lymph node subscapular sinus macrophages are reduced in diphtheria toxin-treated mice
• however, F4/80+ medullar macrophages in the skin lymph nodes are unaffected in diphtheria toxin-treated mice
• in diphtheria toxin-treated mice
• reduced IFNgamma+ CD3+CD4+ T cells in diphtheria toxin-treated bone marrow chimeras immunized with either alpha-DEC-205-GAGp24 or alpha-Treml4-GAGp24, or infected with T. gondii
• diphtheria toxin-treated bone marrow chimeras exhibit fail to exhibit an antitumor memory response unlike control mice and Zbtb46tm1(HBEGF)Mnz heterozygotes





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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory