About   Help   FAQ
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 (11 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 (11 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





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/23/2024
MGI 6.23
The Jackson Laboratory