- decreased hematocrit / MGI
- abnormal vascular development / MGI
- small liver / MGI
- pale liver / MGI
- enlarged spleen / MGI
- spleen hyperplasia / MGI
- decreased thymocyte number / MGI
- anemia / MGI
- impaired hematopoiesis / MGI
- decreased embryo size / MGI
- pale yolk sac / MGI
- abnormal humoral immune response / MGI
- intracranial hemorrhage / MGI
- intraventricular hemorrhage / MGI
- increased leukemia incidence / MGI
- abnormal B cell differentiation / MGI
- abnormal megakaryocyte progenitor cell morphology / MGI
- abnormal proerythroblast morphology / MGI
- abnormal megakaryocyte morphology / MGI
- abnormal class switch recombination / MGI
- decreased B cell number / MGI
- decreased B cell proliferation / MGI
- spinal hemorrhage / MGI
- decreased follicular B cell number / MGI
- increased marginal zone B cell number / MGI
- increased transitional stage B cell number / MGI
- decreased megakaryocyte cell number / MGI
- decreased IgG1 level / MGI
- decreased IgG3 level / MGI
- abnormal splenic cell ratio / MGI
- abnormal brain meninges morphology / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
B6;129-Fli1tm1Morl/Orl
| Status | Available to order |
| EMMA ID | EM:05991 |
| Citation information | RRID:IMSR_EM:05991 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
| International strain name | B6;129-Fli1tm1Morl/Orl |
| Alternative name | Fli1-fl/fl |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Fli1tm1Morl |
| Gene/Transgene symbol | Fli1 |
Information from provider
| Provider | Francois Morle |
| Provider affiliation | CGPhyMC , CNRS UMR5534 |
| Genetic information | This strain carries two loxP sequences flanking the whole coding region of Fli1 gene exon 9 that have been inserted in intron 8 and 3' UTR respectively. The FRT flanked neo gene cassette initially inserted in 3' UTR and used to select homologous recombinant ES cells clones has been removed by transient FLP expression before generating the transgenic founder of this strain. This strain allows conditional Cre-mediated deletion of Fli1 gene exon 9 encoding the whole DNA-binding and C-terminal regions of Fli1 transcription factor. |
| Phenotypic information | Contrasting with lethality of Fli1 -/- genotype, homozygous Fli1 flox/flox mice are viable and fertile and display no obvious phenotype. Cre recombinase induction in homozygous Fli1 flox/flox Mx1-cre+ or heterozygous Fli1 flox/- Mx1-cre+ mice leads to multiple commitment decisions and proliferation/differentiation alterations in adult hematopoiesis. |
| Breeding history | LoxP insertions at Fli1 locus were generated in 129P2 ES cells. Cells were injected in C57BL/6J blastocysts and backcrossed on C57BL/6J. |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | CNRS-TAAM – Typing and Archiving of Animal Models, Orléans, France |
| Animals used for archiving | homozygous C57BL/6J males, wild-type C57BL/6J females |
| Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Isolated delta-storage pool disease / Orphanet_248340
MGI phenotypes (gene matching)
Literature references
- Inducible Fli-1 gene deletion in adult mice modifies several myeloid lineage commitment decisions and accelerates proliferation arrest and terminal erythrocytic differentiation.;Starck Joëlle, Weiss-Gayet Michèle, Gonnet Colette, Guyot Boris, Vicat Jean-Michel, Morlé François, ;2010;Blood;116;4795-805; 20733157
Information on how we integrate external resources can be found here
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