C57BL/6NCrl-Gfi1bem1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:15145 |
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
IMPC phenotypes (gene matching)
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
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