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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fli1tm1Dkw
targeted mutation 1, Dennis K Watson
MGI:2386167
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Fli1tm1Dkw/Fli1tm1Dkw either: B6.Cg-Fli1tm1Dkw or (involves: CD-1) or (involves: 129S6/SvEvTac * C57BL/6) MGI:3056158
cx2
Fli1tm1Dkw/Fli1+
Mpltm1Wsa/Mpltm1Wsa
involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 MGI:3805477


Genotype
MGI:3056158
hm1
Allelic
Composition
Fli1tm1Dkw/Fli1tm1Dkw
Genetic
Background
either: B6.Cg-Fli1tm1Dkw or (involves: CD-1) or (involves: 129S6/SvEvTac * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fli1tm1Dkw mutation (1 available); any Fli1 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygous mutant embryos exhibit no overt defects until E11.0 but die by E12.5

cardiovascular system
• at E11.0, fetal blood also hemorrhages into the cephalic ventricles
• at E11.0, all homozygotes are severely hematorrhachitic: they hemorrhage from the dorsal aorta into the lumen of the neural tube
• at E11.0, all homozygotes show an impaired columnar neuroepithelium, a reduced adjacent extracellular matrix, and a hematoma at the site of hemorrhage

embryo
• at E11.0, homozygotes dissected free of the yolk sac are visibly smaller than wild-type
• at E11.0, all homozygotes show a complete absence of red cells in the yolk sac vasculature

growth/size/body
• at E11.0, homozygotes dissected free of the yolk sac are visibly smaller than wild-type

hematopoietic system
• cultures of progenitors from mutant yolk sacs show reduced levels of CFU-mix: neutrophils, macrophages, mast cells, and erythroid cells, but not megakaryocytes, are present
• at E11.0, mutant fetal liver cells display defects in hematopoietic colony formation, including a severe reduction in the number of pronormoblasts and basophilic normoblasts
• at E11.0, the predominant cells present in mutant fetal livers are orthochromatic and polychromatophilic normoblasts; some of these display megaloblastoid changes
• cells from the aorta-gonad-mesonephros region (AGM) of E10.0 homozygotes show a significant reduction in the number of megakaryocytes relative to wild-type
• AGM cells from E10.0 homozygotes show a significant reduction in the % of pronormoblasts and basophilic normoblasts and contain predominantly orthochromatic and polychromatophilic normoblasts

liver/biliary system
• at E11.0, the developing livers of homozygotes are smaller than those of wild-type
• at E11.0, the developing livers of homozygotes appear to be pale

nervous system
• at E11.0, fetal blood also hemorrhages into the cephalic ventricles
• at E11.0, all homozygotes are severely hematorrhachitic: they hemorrhage from the dorsal aorta into the lumen of the neural tube
• at E11.0, all homozygotes show an impaired columnar neuroepithelium, a reduced adjacent extracellular matrix, and a hematoma at the site of hemorrhage




Genotype
MGI:3805477
cx2
Allelic
Composition
Fli1tm1Dkw/Fli1+
Mpltm1Wsa/Mpltm1Wsa
Genetic
Background
involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fli1tm1Dkw mutation (1 available); any Fli1 mutation (26 available)
Mpltm1Wsa mutation (1 available); any Mpl mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
N
• mice do not show leukopenia or anemia
• platelet counts are lower than single Mpl-deficient littermates at 7 weeks of age





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