- abnormal immune system morphology / MGI
- decreased IgG level / MGI
- decreased IgM level / MGI
- abnormal B cell differentiation / MGI
- abnormal T cell differentiation / MGI
- abnormal spleen marginal zone morphology / MGI
- abnormal dendritic cell physiology / MGI
- abnormal double-negative T cell morphology / MGI
- decreased immunoglobulin level / MGI
- abnormal T cell proliferation / MGI
- decreased T cell proliferation / MGI
- absent B-1a cells / MGI
- decreased interleukin-2 secretion / MGI
- impaired humoral immune response / MGI
B6.129P2-Malt1tm1Mak/Cnbc
Status | Available to order |
EMMA ID | EM:06391 |
Citation information | RRID:IMSR_EM:06391 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 | B6.129P2-Malt1tm1Mak/Cnbc |
Alternative name | Malt1 |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Malt1tm1Mak |
Gene/Transgene symbol | Malt1 |
Information from provider
Provider | Tak W Mak |
Provider affiliation | Mak Lab, Campbell Family Breast Cancer reseach Institute |
Genetic information | Deletion of exon 8 with the neo targeting vector in antisense. |
Phenotypic information | Malt1 is essential for T cell activation, proliferation, and IL-2 production in response to TCR ligation and strictly required for signal-specific NF-kappaB activation induced by the TCR, but not TNF-alpha or IL-1 signaling. |
Breeding history | Backcrossed 10 times to C57BL/6. |
References |
|
Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | yes |
Information from EMMA
Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Animals used for archiving | heterozygous C57BL/6J males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Combined immunodeficiency due to MALT1 deficiency / Orphanet_397964
MGI phenotypes (gene matching)
Literature references
- Differential requirement for Malt1 in T and B cell antigen receptor signaling.;Ruland Jürgen, Duncan Gordon S, Wakeham Andrew, Mak Tak W, ;2003;Immunity;19;749-58; 14614861
- The NF-κB regulator MALT1 determines the encephalitogenic potential of Th17 cells.;Brüstle Anne, Brenner Dirk, Knobbe Christiane B, Lang Philipp A, Virtanen Carl, Hershenfield Brian M, Reardon Colin, Lacher Sonja M, Ruland Jürgen, Ohashi Pamela S, Mak Tak W, ;2012;The Journal of clinical investigation;122;4698-709; 23114599
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