- increased granulocyte number / MGI
- abnormal spleen morphology / MGI
- spleen hypoplasia / MGI
- decreased body size / MGI
- arrested B cell differentiation / MGI
- decreased IgM level / MGI
- thymus hypoplasia / MGI
- arrested T cell differentiation / MGI
- increased susceptibility to infection / MGI
- abnormal effector T cell morphology / MGI
- increased natural killer cell mediated cytotoxicity / MGI
- decreased double-positive T cell number / MGI
- increased macrophage cell number / MGI
- decreased CD4-positive, alpha beta T cell number / MGI
- decreased CD8-positive, alpha-beta T cell number / MGI
- lymph node hypoplasia / MGI
- absent mature B cells / MGI
- abnormal T cell receptor V(D)J recombination / MGI
- abnormal immunoglobulin V(D)J recombination / MGI
- decreased thymocyte number / MGI
- lung inflammation / MGI
- increased susceptibility to bacterial infection / MGI
- abnormal macrophage physiology / MGI
- colitis / MGI
- abnormal T-helper 1 physiology / MGI
- abnormal response to transplant / MGI
- abnormal interferon secretion / MGI
- abnormal chemokine secretion / MGI
- decreased susceptibility to bacterial infection induced morbidity/mortality / MGI
- abnormal intestinal mucosa morphology / MGI
- abnormal B cell morphology / MGI
- decreased susceptibility to parasitic infection / MGI
- decreased double-negative T cell number / MGI
- increased double-negative T cell number / MGI
- decreased susceptibility to type IV hypersensitivity reaction / MGI
- abnormal stomach mucosa morphology / MGI
- abnormal intestinal epithelium morphology / MGI
- abnormal B cell number / MGI
- decreased pre-B cell number / MGI
- decreased mature B cell number / MGI
- increased immature B cell number / MGI
- decreased immature B cell number / MGI
- abnormal gamma-delta T cell differentiation / MGI
B6.Cg-Ptprca Rag2tm1Fwa Tg(Tcra-V19-J33)#Lantz Tg(Tcrb-V6)#Lantz/Orl
| Status | Available to order |
| EMMA ID | EM:04508 |
| Citation information | RRID:IMSR_EM:04508 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-Ptprca Rag2tm1Fwa Tg(Tcra-V19-J33)#Lantz Tg(Tcrb-V6)#Lantz/Orl |
| Alternative name | iVa19/Vb6 RAG ko/ko CD45.1 |
| Strain type | Transgenic Strains |
| Allele/Transgene symbol | Tg(Tcra-V19-J33)#Lantz, Tg(Tcrb-V6)#Lantz, Rag2tm1Fwa, Ptprca |
| Gene/Transgene symbol | Tg(Tcra-V19-J33)#Lantz, Tg(Tcrb-V6)#Lantz, Rag2, Ptprc |
Information from provider
| Provider | Olivier Lantz |
| Provider affiliation | immunology, Institut Curie |
| Genetic information | The VJ alpha (Va19-Ja33) and beta (Vb6) of mucosal-associated invariant T (MAIT) cell hybridoma have been inserted into the shuttle vector described by Patten et al. (J Immunol. 1993;150(6):2281-94). The Va19-Ja33 transgene was introduced into B6 x DBA/2 eggs before being backcrossed 10 times to C57BL/6J. The Vb6 transgene was injected into C57BL/6 eggs and the founder line was crossed to Va19 transgenic on a B6 Rag2 knock-out, Ptprca (CD45.1) background. |
| Phenotypic information | The strain expresses a monoclonal population of mucosal-associated invariant T (MAIT) cells. |
| Breeding history | The strain is a double transgenic (independently injected and thus not linked), Rag2 knock-out and Ptprca (CD45.1) congenic. It is immunodeficient and requires homozygous breeding. |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | yes |
| Immunocompromised | yes |
Information from EMMA
| Archiving centre | CNRS-TAAM – Typing and Archiving of Animal Models, Orléans, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- T-B+ severe combined immunodeficiency due to CD45 deficiency / Orphanet_169157
- Severe combined immunodeficiency due to complete RAG1/2 deficiency / Orphanet_331206
- Omenn syndrome / Orphanet_39041
- Combined immunodeficiency with granulomatosis / Orphanet_157949
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal long bone metaphysis morphology / MGI
- abnormal leukocyte cell number / MGI
- increased neutrophil cell number / MGI
- decreased leukocyte cell number / MGI
- extramedullary hematopoiesis / MGI
- abnormal erythropoiesis / MGI
- enlarged spleen / MGI
- spleen hyperplasia / MGI
- enlarged lymph nodes / MGI
- decreased thymocyte number / MGI
- abnormal immune system cell morphology / MGI
- abnormal myelination / MGI
- abnormal oligodendrocyte morphology / MGI
- abnormal osteoclast physiology / MGI
- abnormal digestion / MGI
- abnormal immune system physiology / MGI
- abnormal humoral immune response / MGI
- thymus hypoplasia / MGI
- arrested T cell differentiation / MGI
- abnormal T cell activation / MGI
- liver inflammation / MGI
- lung inflammation / MGI
- premature death / MGI
- abnormal T cell differentiation / MGI
- no abnormal phenotype detected / MGI
- abnormal bone marrow cell morphology/development / MGI
- abnormal lymphopoiesis / MGI
- abnormal double-positive T cell morphology / MGI
- increased susceptibility to viral infection / MGI
- abnormal T cell physiology / MGI
- abnormal B cell number / MGI
- increased IgA level / MGI
- abnormal immune system organ morphology / MGI
- glomerulonephritis / MGI
- increased urine protein level / MGI
- abnormal cytokine secretion / MGI
- no phenotypic analysis / MGI
- kidney failure / MGI
- oliguria / MGI
- abnormal thymocyte activation / MGI
- abnormal T cell subpopulation ratio / MGI
- increased anti-double stranded DNA antibody level / MGI
- abnormal T cell selection / MGI
- abnormal positive T cell selection / MGI
- increased B-1 B cell number / MGI
- abnormal osteoclast morphology / MGI
- increased B cell number / MGI
- increased T cell number / MGI
- decreased B cell number / MGI
- decreased T cell number / MGI
- abnormal response to infection / MGI
- diarrhea / MGI
- decreased cytotoxic T cell cytolysis / MGI
- increased double-negative T cell number / MGI
- decreased double-positive T cell number / MGI
- decreased B cell proliferation / MGI
- decreased T cell proliferation / MGI
- increased susceptibility to autoimmune disorder / MGI
- immune system phenotype / MGI
- hematopoietic system phenotype / MGI
- decreased susceptibility to type I hypersensitivity reaction / MGI
- CNS inflammation / MGI
- increased T cell apoptosis / MGI
- abnormal T cell morphology / MGI
- increased NK cell number / MGI
- abnormal memory T cell number / MGI
- increased memory T cell number / MGI
- decreased memory T cell number / MGI
- absent T cells / MGI
- decreased CD4-positive, alpha beta T cell number / MGI
- abnormal CD4-positive T cell differentiation / MGI
- decreased CD8-positive, alpha-beta T cell number / MGI
- abnormal CD8-positive, alpha-beta T cell differentiation / MGI
- increased single-positive T cell number / MGI
- decreased single-positive T cell number / MGI
- increased plasma cell number / MGI
- lymph node hyperplasia / MGI
- abnormal granulocyte differentiation / MGI
- increased dendritic cell number / MGI
- decreased B-1a cell number / MGI
- increased B-1b cell number / MGI
- decreased B-1b cell number / MGI
- decreased follicular B cell number / MGI
- increased transitional stage B cell number / MGI
- abnormal follicular B cell physiology / MGI
- decreased B-2 B cell number / MGI
- decreased mature B cell number / MGI
- abnormal B cell activation / MGI
- abnormal leukocyte morphology / MGI
- decreased gamma-delta intraepithelial T cell number / MGI
- abnormal CD4-positive, alpha-beta intraepithelial T cell morphology / MGI
- increased spleen red pulp amount / MGI
- increased spleen white pulp amount / MGI
- increased IgG2a level / MGI
- increased plasmacytoid dendritic cell number / MGI
- abnormal chemokine secretion / MGI
- decreased memory B cell number / MGI
- decreased mast cell degranulation / MGI
- abnormal intraepithelial T cell morphology / MGI
- abnormal intraepithelial T cell number / MGI
- decreased oligodendrocyte number / MGI
- increased DN3 thymocyte number / MGI
- decreased DN4 thymocyte number / MGI
- abnormal NK cell physiology / MGI
- mortality/aging / MGI
- decreased CD4-positive, alpha-beta memory T cell number / MGI
- decreased CD8-positive, alpha-beta memory T cell number / MGI
- lethality at weaning, incomplete penetrance / MGI
- increased alpha-beta T cell number / MGI
- decreased CD8-positive, naive alpha-beta T cell number / MGI
- decreased monocyte cell number / MGI
- increased granulocyte number / MGI
- decreased bone marrow cell number / MGI
- alopecia / MGI
- abnormal digestive system morphology / MGI
- abnormal intestinal epithelium morphology / MGI
- abnormal intestinal mucosa morphology / MGI
- abnormal spleen morphology / MGI
- small spleen / MGI
- spleen hypoplasia / MGI
- abnormal Peyer's patch morphology / MGI
- abnormal thymus morphology / MGI
- decreased thymocyte number / MGI
- abnormal immune system cell morphology / MGI
- decreased body size / MGI
- abnormal humoral immune response / MGI
- arrested B cell differentiation / MGI
- decreased IgG level / MGI
- decreased IgM level / MGI
- decreased IgA level / MGI
- thymus hypoplasia / MGI
- arrested T cell differentiation / MGI
- lung inflammation / MGI
- neoplasm / MGI
- abnormal B cell differentiation / MGI
- no abnormal phenotype detected / MGI
- small lymph nodes / MGI
- abnormal lymph node morphology / MGI
- abnormal lymphopoiesis / MGI
- abnormal pre-B cell morphology / MGI
- increased susceptibility to infection / MGI
- abnormal double-negative T cell morphology / MGI
- abnormal double-positive T cell morphology / MGI
- increased susceptibility to bacterial infection / MGI
- abnormal effector T cell morphology / MGI
- abnormal macrophage physiology / MGI
- abnormal B cell number / MGI
- abnormal B cell physiology / MGI
- abnormal immune system organ morphology / MGI
- colitis / MGI
- absent Peyer's patches / MGI
- increased natural killer cell mediated cytotoxicity / MGI
- erythroderma / MGI
- abnormal lymphocyte physiology / MGI
- abnormal B cell morphology / MGI
- decreased lymphocyte cell number / MGI
- decreased B cell number / MGI
- decreased T cell number / MGI
- decreased susceptibility to parasitic infection / MGI
- decreased double-negative T cell number / MGI
- increased double-negative T cell number / MGI
- decreased double-positive T cell number / MGI
- decreased T cell proliferation / MGI
- cachexia / MGI
- increased macrophage cell number / MGI
- abnormal T-helper 1 physiology / MGI
- decreased susceptibility to type IV hypersensitivity reaction / MGI
- abnormal response to transplant / MGI
- abnormal T cell morphology / MGI
- decreased NK T cell number / MGI
- decreased CD4-positive, alpha beta T cell number / MGI
- decreased CD8-positive, alpha-beta T cell number / MGI
- lymph node hypoplasia / MGI
- decreased pre-B cell number / MGI
- decreased mature B cell number / MGI
- absent mature B cells / MGI
- increased immature B cell number / MGI
- decreased immature B cell number / MGI
- abnormal gamma-delta T cell differentiation / MGI
- decreased spleen white pulp amount / MGI
- abnormal interferon secretion / MGI
- abnormal chemokine secretion / MGI
- abnormal T cell receptor V(D)J recombination / MGI
- abnormal immunoglobulin V(D)J recombination / MGI
- absent Hassall's corpuscle / MGI
- small inguinal lymph nodes / MGI
- decreased susceptibility to bacterial infection induced morbidity/mortality / MGI
- increased DN3 thymocyte number / MGI
- abnormal stomach mucosa morphology / MGI
- small cervical lymph nodes / MGI
Literature references
- Stepwise development of MAIT cells in mouse and human.;Martin Emmanuel, Treiner Emmanuel, Duban Livine, Guerri Lucia, Laude Hélène, Toly Cécile, Premel Virginie, Devys Anne, Moura Ivan C, Tilloy Florence, Cherif Stéphane, Vera Gabriella, Latour Sylvain, Soudais Claire, Lantz Olivier, ;2009;PLoS biology;7;e54; 19278296
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