IMPC phenotypes (gene matching)
C57BL/6NCrl-Gfi1bem1(IMPC)Ccpcz/Ph
| Status | Under development - register interest |
| EMMA ID | EM:15145 |
| Citation information | RRID:IMSR_EM:15145 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 | C57BL/6NCrl-Gfi1bem1(IMPC)Ccpcz/Ph |
| Alternative name | |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Gfi1bem1(IMPC)Ccpcz |
| Gene/Transgene symbol | Gfi1b |
Information from provider
| Provider | Institute of Molecular Genetics |
| Provider affiliation | Department of Transgenic Models of Diseases, Institute of Molecular Genetics |
| Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
| Phenotypic information | Potential phenotyping data in the IMPC portal |
| References | None available |
Information from EMMA
| Archiving centre | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Gray platelet syndrome / Orphanet_721
- Autosomal dominant macrothrombocytopenia / Orphanet_140957
- Alpha delta granule deficiency / Orphanet_734
MGI phenotypes (gene matching)
- absent erythrocytes / MGI
- abnormal megakaryocyte differentiation / MGI
- abnormal erythropoiesis / MGI
- internal hemorrhage / MGI
- edema / MGI
- hemorrhage / MGI
- pallor / MGI
- abnormal embryonic erythropoiesis / MGI
- abnormal embryonic erythrocyte morphology / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI