About   Help   FAQ
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





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
12/10/2024
MGI 6.24
The Jackson Laboratory