- 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
C57BL/6N-Malt1tm1b(EUCOMM)Hmgu/H
| Status | Under development - register interest |
| EMMA ID | EM:16809 |
| Citation information | RRID:IMSR_EM:16809 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 | C57BL/6N-Malt1tm1b(EUCOMM)Hmgu/H |
| Alternative name | C57BL/6N-Malt1 |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Malt1tm1b(EUCOMM)Hmgu |
| Gene/Transgene symbol | Malt1 |
Information from provider
| Provider | MRC, Medical Research Council |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | This mouse line originates from ESC clone HEPD0618_3_A10. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele . For further details on the construction of this clone see the page at the IMPC portal |
| Phenotypic information | Homozygous:These mice are part of the International Mouse Phenotyping Consortium (IMPC) and will be phenotyped through a standardised phenotyping pipeline. Details of the pipeline and data, when available, can be viewed at www.mousephenotype.orgHeterozygous:These mice are part of the International Mouse Phenotyping Consortium (IMPC) and will be phenotyped through a standardised phenotyping pipeline. Details of the pipeline and data, when available, can be viewed at www.mousephenotype.org |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | not known |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
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)
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).
