- increased circulating insulin level / IMPC
- decreased lean body mass / IMPC
- increased mean corpuscular hemoglobin / IMPC
- increased blood urea nitrogen level / IMPC
- increased mean corpuscular hemoglobin concentration / IMPC
- absent pinna reflex / IMPC
- increased total body fat amount / IMPC
- increased red blood cell distribution width / IMPC
C57BL/6N-Kmt2etm1.2(IMPC)Wtsi/WtsiOrl
Status | Available to order |
EMMA ID | EM:14411 |
International strain name | C57BL/6N-Kmt2etm1.2(IMPC)Wtsi/WtsiOrl |
Alternative name | BEPD0111_B03 |
Strain type | |
Allele/Transgene symbol | Kmt2etm1.2(IMPC)Wtsi |
Gene/Transgene symbol | Kmt2e |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from undef ES clone BEPD0111_B03. For further details on the construction of this clone see the page at the IMPC portal. ES cells were generated using the CRISPR/Cas9 technology. The details of the applied experimental procedures involving CRISPR/Cas9 technology are not available. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Non-specific syndromic intellectual disability / Orphanet_528084
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- decreased lean body mass / IMPC
- increased total body fat amount / IMPC
- absent pinna reflex / IMPC
- increased circulating insulin level / IMPC
- increased mean corpuscular hemoglobin / IMPC
- increased red blood cell distribution width / IMPC
- increased blood urea nitrogen level / IMPC
- increased mean corpuscular hemoglobin concentration / IMPC
MGI phenotypes (gene matching)
- decreased hematocrit / MGI
- increased neutrophil cell number / MGI
- decreased leukocyte cell number / MGI
- small spleen / MGI
- spleen hypoplasia / MGI
- small thymus / MGI
- decreased thymocyte number / MGI
- decreased body weight / MGI
- decreased body size / MGI
- increased mortality induced by gamma-irradiation / MGI
- postnatal growth retardation / MGI
- thymus hypoplasia / MGI
- reduced female fertility / MGI
- male infertility / MGI
- abnormal definitive hematopoiesis / MGI
- small lymph nodes / MGI
- abnormal bone marrow cell morphology/development / MGI
- abnormal lymphopoiesis / MGI
- increased susceptibility to bacterial infection / MGI
- abnormal myeloblast morphology/development / MGI
- abnormal neutrophil differentiation / MGI
- abnormal neutrophil physiology / MGI
- low mean erythrocyte cell number / MGI
- globozoospermia / MGI
- decreased hemoglobin content / MGI
- decreased erythrocyte cell number / MGI
- no phenotypic analysis / MGI
- thrombocytopenia / MGI
- decreased macrophage cell number / MGI
- abnormal hematopoietic stem cell morphology / MGI
- increased hematopoietic stem cell number / MGI
- decreased hematopoietic stem cell number / MGI
- decreased B cell number / MGI
- decreased T cell number / MGI
- decreased double-negative T cell number / MGI
- decreased double-positive T cell number / MGI
- blepharitis / MGI
- immune system phenotype / MGI
- hematopoietic system phenotype / MGI
- decreased NK T cell number / MGI
- decreased NK cell number / MGI
- abnormal granulocyte differentiation / MGI
- decreased pro-B cell number / MGI
- decreased pre-B cell number / MGI
- decreased common myeloid progenitor cell number / MGI
- increased hemoglobin concentration distribution width / MGI
- decreased total body fat amount / MGI
- postnatal lethality, complete penetrance / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- lethality during fetal growth through weaning, incomplete penetrance / MGI
- dilated seminal vesicles / MGI
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