- increased body weight / IMPC
- abnormal lens morphology / IMPC
- cataract / IMPC
- abnormal urination / IMPC
- decreased circulating triglyceride level / IMPC
- abnormal bone mineralization / IMPC
- thrombocytopenia / IMPC
- increased lean body mass / IMPC
- abnormal vertebral arch morphology / IMPC
- vertebral fusion / IMPC
- abnormal behavior / IMPC
- decreased T cell number / IMPC
- decreased circulating cholesterol level / IMPC
- increased total body fat amount / IMPC
- increased grip strength / IMPC
- increased bone mineral content / IMPC
- preweaning lethality, complete penetrance / IMPC
C57BL/6NTac-Xbp1tm1a(EUCOMM)Wtsi/IcsOrl
Status | Available to order |
EMMA ID | EM:07516 |
International strain name | C57BL/6NTac-Xbp1tm1a(EUCOMM)Wtsi/IcsOrl |
Alternative name | EPD0038_2_E10 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Xbp1tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Xbp1 |
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 | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0038_2_E10. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac, wild-type C57BL/6NTac |
Stage of embryos | 8-cell |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- decreased circulating triglyceride level / IMPC
- abnormal behavior / IMPC
- decreased T cell number / IMPC
- thrombocytopenia / IMPC
- increased grip strength / IMPC
- increased mean corpuscular volume / IMPC
- preweaning lethality, complete penetrance / IMPC
- increased total body fat amount / IMPC
- increased mean corpuscular hemoglobin / IMPC
- persistence of hyaloid vascular system / IMPC
- decreased leukocyte cell number / IMPC
- cataract / IMPC
- decreased large unstained cell number / IMPC
- decreased red blood cell distribution width / IMPC
- decreased circulating cholesterol level / IMPC
- increased lean body mass / IMPC
- abnormal lens morphology / IMPC
- vertebral fusion / IMPC
- decreased lymphocyte cell number / IMPC
- increased bone mineral content / IMPC
- abnormal bone mineralization / IMPC
- increased body weight / IMPC
- abnormal vertebral arch morphology / IMPC
- abnormal urination / IMPC
MGI phenotypes (gene matching)
- abnormal heart development / MGI
- thin ventricular wall / MGI
- enlarged pericardium / MGI
- absent trabeculae carneae / MGI
- decreased cell proliferation / MGI
- abnormal liver development / MGI
- liver hypoplasia / MGI
- small liver / MGI
- wavy neural tube / MGI
- anemia / MGI
- impaired hematopoiesis / MGI
- abnormal blood vessel morphology / MGI
- decreased embryo size / MGI
- anoxia / MGI
- pallor / MGI
- increased hepatocyte apoptosis / MGI
- embryonic growth retardation / MGI
- decreased hepatocyte proliferation / MGI
- abnormal extraembryonic tissue physiology / MGI
- myocardial necrosis / MGI
- decreased embryo weight / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- embryo tissue necrosis / MGI
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