- enlarged spleen / MGI
- abnormal Peyer's patch morphology / MGI
- decreased thymocyte number / MGI
- scaly skin / MGI
- dermatitis / MGI
- weight loss / MGI
- thymus hypoplasia / MGI
- conjunctivitis / MGI
- liver inflammation / MGI
- lung inflammation / MGI
- abnormal T cell differentiation / MGI
- no abnormal phenotype detected / MGI
- abnormal dendritic cell physiology / MGI
- abnormal gut-associated lymphoid tissue morphology / MGI
- no phenotypic analysis / MGI
- lymph node inflammation / MGI
- abnormal regulatory T cell morphology / MGI
- increased regulatory T cell number / MGI
- decreased regulatory T cell number / MGI
- increased T cell number / MGI
- decreased T cell number / MGI
- decreased double-positive T cell number / MGI
- cachexia / MGI
- bradykinesia / MGI
- abnormal mesenteric lymph node morphology / MGI
- increased susceptibility to autoimmune disorder / MGI
- immune system phenotype / MGI
- abnormal CD4-positive, alpha-beta T cell physiology / MGI
- increased susceptibility to type IV hypersensitivity reaction / MGI
- increased T cell apoptosis / MGI
- increased dendritic cell number / MGI
- abnormal intraepithelial T cell morphology / MGI
- increased sensitivity to induced morbidity/mortality / MGI
- mortality/aging / MGI
B6.Cg-Foxp3tm1.1Mal/Orl
Status | Available to order |
EMMA ID | EM:01945 |
Citation information | RRID:IMSR_EM:01945 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.Cg-Foxp3tm1.1Mal/Orl |
Alternative name | B6-FoxP3tm1mal, FoxP3 EGFP |
Strain type | Targeted Mutant Strains : Knock-in |
Allele/Transgene symbol | Foxp3.1tm1Mal |
Gene/Transgene symbol | Foxp3 |
Information from provider
Provider | Bernard Malissen |
Provider affiliation | Centre D |
Genetic information | An IRES-EGFP cassette was introduced in the 3'-UTR region of Foxp3 gene, exon11. The autodeleter neomycin-cre recombinase cassette was used. |
Phenotypic information | EGFP labels all regulatory T cells. Very specific labeling, all EGFP+ cells are FOXP3+. |
References |
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Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome / Orphanet_37042
MGI phenotypes (gene matching)
Literature references
- Th2 lymphoproliferative disorder of LatY136F mutant mice unfolds independently of TCR-MHC engagement and is insensitive to the action of Foxp3+ regulatory T cells.;Wang Ying, Kissenpfennig Adrien, Mingueneau Michael, Richelme Sylvie, Perrin Pierre, Chevrier Stéphane, Genton Céline, Lucas Bruno, DiSanto James P, Acha-Orbea Hans, Malissen Bernard, Malissen Marie, ;2008;Journal of immunology (Baltimore, Md. : 1950);180;1565-75; 18209052
- Foxp3+ Regulatory and Conventional CD4+ T Cells Display Similarly High Frequencies of Alloantigen-Reactive Cells.;Lalfer Mélanie, Chappert Pascal, Carpentier Maxime, Urbain Dominique, Davoust Jean M, Gross David-Alexandre, ;2019;Frontiers in immunology;10;521; 30941146
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