- process of degenerative change / IMPC
- decreased circulating glucose level / IMPC
- hyperactivity / IMPC
- decreased hemoglobin content / IMPC
- impaired pupillary reflex / IMPC
- decreased sacral vertebrae number / IMPC
- decreased mean corpuscular hemoglobin / IMPC
- increased lumbar vertebrae number / IMPC
- decreased circulating iron level / IMPC
- increased blood uric acid level / IMPC
- vertebral fusion / IMPC
- corneal opacity / IMPC
- cataract / IMPC
- decreased hematocrit / IMPC
- preweaning lethality, complete penetrance / IMPC
- decreased mean corpuscular volume / IMPC
- abnormal cornea morphology / IMPC
C57BL/6NTac-Asxl1tm1e(EUCOMM)Wtsi/Cnrm
Status | Available to order |
EMMA ID | EM:03996 |
International strain name | C57BL/6NTac-Asxl1tm1e(EUCOMM)Wtsi/Cnrm |
Alternative name | EPD0080_1_B11 |
Strain type | Targeted Mutant Strains : Targeted Non-conditional |
Allele/Transgene symbol | Asxl1tm1e(EUCOMM)Wtsi |
Gene/Transgene symbol | Asxl1 |
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 | CNR, Consiglio Nazionale delle Ricerche |
Provider affiliation | EMMA-Monterotondo Campus International Development, CNR, Consiglio Nazionale delle Ricerche |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0080_1_B11. For further details on the construction of this clone see the page at the IMPC portal. The targeted allele has lost the 3' loxP site. These mutations cannot be converted into conditional alleles. Click here for more information on EUCOMM final vectors. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Animals used for archiving | heterozygous C57BL/6NTac, wild-type C57BL/6NTac |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Systemic mastocytosis with associated hematologic neoplasm / Orphanet_98849
- Aggressive systemic mastocytosis / Orphanet_98850
- Bohring-Opitz syndrome / Orphanet_97297
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- cleft palate / MGI
- increased leukocyte cell number / MGI
- increased monocyte cell number / MGI
- decreased leukocyte cell number / MGI
- decreased neutrophil cell number / MGI
- extramedullary hematopoiesis / MGI
- increased bone marrow cell number / MGI
- decreased bone marrow cell number / MGI
- increased cell proliferation / MGI
- abnormal craniofacial morphology / MGI
- mandible hypoplasia / MGI
- abnormal liver morphology / MGI
- enlarged liver / MGI
- abnormal spleen morphology / MGI
- enlarged spleen / MGI
- small spleen / MGI
- spleen hyperplasia / MGI
- abnormal thymus morphology / MGI
- abnormal immune system cell morphology / MGI
- decreased body weight / MGI
- decreased body size / MGI
- anophthalmia / MGI
- microphthalmia / MGI
- abnormal cornea morphology / MGI
- corneal opacity / MGI
- anemia / MGI
- abnormal myelopoiesis / MGI
- impaired hematopoiesis / MGI
- increased malignant tumor incidence / MGI
- increased leukemia incidence / MGI
- increased sarcoma incidence / MGI
- premature death / MGI
- abnormal spleen white pulp morphology / MGI
- abnormal bone marrow cell morphology/development / MGI
- abnormal lymphopoiesis / MGI
- abnormal megakaryocyte morphology / MGI
- abnormal blood cell morphology/development / MGI
- abnormal neutrophil physiology / MGI
- opacity of vitreous body / MGI
- abnormal immune system organ morphology / MGI
- decreased hemoglobin content / MGI
- vertebral transformation / MGI
- abnormal hyoid bone morphology / MGI
- thrombocytopenia / MGI
- spleen atrophy / MGI
- vertebral fusion / MGI
- decreased lumbar vertebrae number / MGI
- increased hematopoietic stem cell number / MGI
- decreased hematopoietic stem cell number / MGI
- decreased spleen weight / MGI
- decreased lymphocyte cell number / MGI
- decreased B cell number / MGI
- decreased T cell number / MGI
- abnormal neutrophil morphology / MGI
- increased double-negative T cell number / MGI
- polychromatophilia / MGI
- abnormal skeleton morphology / MGI
- decreased circulating glucose level / MGI
- decreased mean corpuscular hemoglobin / MGI
- increased apoptosis / MGI
- abnormal common myeloid progenitor cell morphology / MGI
- decreased CD4-positive, alpha beta T cell number / MGI
- increased single-positive T cell number / MGI
- decreased pre-B cell number / MGI
- abnormal leukocyte morphology / MGI
- decreased spleen red pulp amount / MGI
- increased blood uric acid level / MGI
- decreased erythroid progenitor cell number / MGI
- eye opacity / MGI
- increased sacral vertebrae number / MGI
- increased number of Howell-Jolly bodies / MGI
- myeloid hyperplasia / MGI
- abnormal hematopoietic stem cell physiology / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- lethality throughout fetal growth and development, incomplete penetrance / MGI
- lethality, complete penetrance / MGI
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