- alopecia / MGI
- reddish skin / MGI
- dermatitis / MGI
- skin lesions / MGI
- thick epidermis / MGI
- epidermal hyperplasia / MGI
- mixed cellular infiltration to dermis / MGI
- abnormal immune system physiology / MGI
- abnormal dendritic cell physiology / MGI
- abnormal dendritic cell antigen presentation / MGI
- increased IgE level / MGI
- increased eosinophil cell number / MGI
- increased double-positive T cell number / MGI
- reproductive system phenotype / MGI
- increased circulating interleukin-18 level / MGI
- increased circulating interleukin-1 beta level / MGI
- increased interleukin-4 secretion / MGI
- increased interleukin-5 secretion / MGI
B6.129S-Ctse129S/SvHsd/H
| Status | Available to order |
| EMMA ID | EM:05213 |
| Citation information | RRID:IMSR_EM:05213 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 | B6.129S-Ctse129S/SvHsd/H |
| Alternative name | C57Bl_CTSEhigh |
| Strain type | Spontaneous |
| Allele/Transgene symbol | Ctse129S/SvHsd |
| Gene/Transgene symbol | Ctse |
Information from provider
| Provider | Benny Chain |
| Provider affiliation | CBU, UCL |
| Genetic information | Cathepsin E is expressed in both haemopoietic and non-haemopoietic tissue. We previously described a natural mutation in the cathepsin E promoter (see reference below) which confers a low expressor phenotype in haemopoietic tissue of C57BL strains. Since this strain is widely used for immunological studies, we have backcrossed the cathepsin E high allele from 129/Sv mice into the C57BL/6J background for eight generations. |
| Phenotypic information | Mice breed normally. No obvious phenotype has been described as yet but cathepsin E has been implicated in regulation of antigen processing, and other aspects of innate immunity. The mice are maintained on 129/Sv background as well as C57BL/6 because there is a natural polymorphism which makes C57BL/6 mice a low expressing strain. |
| Breeding history | 129/Sv mouse was backcrossed repeatedly onto the C57BL/6J background. At each generation cathepsin E high genotype was selected for next generation backcross. After 8 generations the mice are maintained by inbreeding of mice with the cathepsin E high allele on a C57BL/6J background. |
| References |
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| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
| Animals used for archiving | homozygous C57BL/6 males |
| Breeding at archiving centre | Males were sperm frozen upon arrival. No breeding was performed at the archiving centre. |
Disease and phenotype information
MGI phenotypes (gene matching)
Literature references
- The expression and function of cathepsin E in dendritic cells.;Chain Benjamin M, Free Paul, Medd Patrick, Swetman Claire, Tabor Alethea B, Terrazzini Nadia, ;2005;Journal of immunology (Baltimore, Md. : 1950);174;1791-800; 15699105
- Natural cathepsin E deficiency in the immune system of C57BL/6J mice.;Tulone Calogero, Tsang Jhen, Prokopowicz Zofia, Grosvenor Nicholas, Chain Benny, ;2007;Immunogenetics;59;927-35; 18000662
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