- 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
C57BL/6NTac-Xbp1tm1c(EUCOMM)Wtsi/IcsOrl
Status | Available to order |
EMMA ID | EM:13138 |
Citation information | RRID:IMSR_EM:13138 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/6NTac-Xbp1tm1c(EUCOMM)Wtsi/IcsOrl |
Alternative name | C57BL/6NTac-Xbp1 tm1c(EUCOMM)Wtsi/IcsOrl |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Xbp1tm1c(EUCOMM)Wtsi |
Gene/Transgene symbol | Xbp1 |
Information from provider
Provider | Cécile FREMOND |
Provider affiliation | CNRS-TAAM-CDTA-UPS44 |
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. The tm1a mice have been crossed with flp recombinase-expressing mice to obtain the tm1c allele. |
Phenotypic information | Homozygous:Homozygous mice have not been generatedHeterozygous:null |
Breeding history | Rederived tm1a mice have been crossed with flp recombinase-expressing mice to obtain the tm1c allele. |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac males |
Disease and phenotype information
IMPC phenotypes (gene matching)
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
Information on how we integrate external resources can be found here
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