- 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 |
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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