- 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 |
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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