- 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 |
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/6N Tac |
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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