- decreased hematocrit / MGI
- abnormal erythropoiesis / MGI
- small liver / MGI
- pale liver / MGI
- enlarged spleen / MGI
- anemia / MGI
- impaired hematopoiesis / MGI
- abnormal erythrocyte morphology / MGI
- anisocytosis / MGI
- poikilocytosis / MGI
- decreased hemoglobin content / MGI
- decreased erythrocyte cell number / MGI
- abnormal erythrocyte osmotic lysis / MGI
- pallor / MGI
- abnormal embryonic erythrocyte morphology / MGI
- abnormal proximal convoluted tubule morphology / MGI
- increased spleen weight / MGI
- erythroblastosis / MGI
- polychromatophilia / MGI
- hematopoietic system phenotype / MGI
- decreased mean corpuscular hemoglobin / MGI
- increased liver iron level / MGI
- increased spleen iron level / MGI
- increased nucleated erythrocyte cell number / MGI
- increased kidney iron level / MGI
- postnatal lethality, incomplete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
C57BL/6N-Klf1em1(IMPC)Wtsi/WtsiIeg
Status | Available to order |
EMMA ID | EM:13779 |
Citation information | RRID:IMSR_EM:13779 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/6N-Klf1em1(IMPC)Wtsi/WtsiIeg |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Klf1em1(IMPC)Wtsi |
Gene/Transgene symbol | Klf1 |
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome / Orphanet_46532
- Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome / Orphanet_251380
- Congenital dyserythropoietic anemia type IV / Orphanet_293825
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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