- 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
STOCK Fli1tm1.1Morl/Orl
| Status | Available to order |
| EMMA ID | EM:05992 |
| Citation information | RRID:IMSR_EM:05992 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 | STOCK Fli1tm1.1Morl/Orl |
| Alternative name | Fli1-KO |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Fli1tm1.1Morl |
| Gene/Transgene symbol | Fli1 |
Information from provider
| Provider | Francois Morle |
| Provider affiliation | CGPhyMC , CNRS UMR5534 |
| Genetic information | This strain carries a single LoxP in place of the whole coding of Fli1 gene exon 9. This strain has been generated by crossing mice harboring Fli1-fl conditional allele with Sycp1Cre mice expressing Cre recombinase during male meiosis. |
| Phenotypic information | Heterozygotes Fli1/Fli1KO have no obvious phenotype. Although not directly tested homozygotes Fli1KO/Fli1KO are expected to die around E12 from hemorrhage and abnormal megakaryopoiesis due to loss of Fli1. |
| 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 | not known |
| Homozygous viable | no |
| 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 | heterozygous C57BL/6J males |
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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