- abnormal skin morphology / IMPC
- increased large unstained cell number / IMPC
- increased grip strength / IMPC
- increased basophil cell number / IMPC
- increased neutrophil cell number / IMPC
- increased eosinophil cell number / IMPC
- increased NK cell number / IMPC
- abnormal cholesterol homeostasis / IMPC
- decreased circulating calcium level / IMPC
- increased lymphocyte cell number / IMPC
- increased effector memory CD8-positive, alpha-beta T cell number / IMPC
- increased circulating aspartate transaminase level / IMPC
- enlarged heart / IMPC
- increased leukocyte cell number / IMPC
- decreased monocyte cell number / IMPC
- abnormal heart morphology / IMPC
- decreased neutrophil cell number / IMPC
C57BL/6N-Tnfrsf1atm2c(EUCOMM)Wtsi/
| Status | Under development - register interest |
| EMMA ID | EM:16818 |
| Citation information | RRID:IMSR_EM:16818 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-Tnfrsf1atm2c(EUCOMM)Wtsi/ |
| Alternative name | C57BL/6N-Tnfrsf1a |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Tnfrsf1atm2c(EUCOMM)Wtsi |
| Gene/Transgene symbol | Tnfrsf1a |
Information from provider
| Provider | MRC, Medical Research Council |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | This line originates from ESC clone EPD0971_5_E01, after breeding with a Flp recombinase deleter line to convert the original targeted allele tm1a (knock-out first allele) into a conditional allele tm1c. 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 | yes |
| Homozygous viable | not known |
| Homozygous matings required | no |
| 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
- Tumor necrosis factor receptor 1 associated periodic syndrome / Orphanet_32960
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- increased bone mineral density / MGI
- abnormal Peyer's patch morphology / MGI
- abnormal sleep pattern / MGI
- abnormal immune system physiology / MGI
- decreased IgG level / MGI
- liver inflammation / MGI
- lung inflammation / MGI
- decreased inflammatory response / MGI
- increased skin papilloma incidence / MGI
- decreased tumor incidence / MGI
- abnormal respiratory mechanics / MGI
- abnormal airway responsiveness / MGI
- abnormal lymph node B cell domain morphology / MGI
- abnormal spleen germinal center morphology / MGI
- abnormal Peyer's patch follicle morphology / MGI
- decreased susceptibility to bacterial infection / MGI
- increased susceptibility to bacterial infection / MGI
- abnormal macrophage physiology / MGI
- granulomatous inflammation / MGI
- impaired skin barrier function / MGI
- abnormal glutamate-mediated receptor currents / MGI
- decreased circulating alanine transaminase level / MGI
- abnormal cytokine secretion / MGI
- no phenotypic analysis / MGI
- abnormal nervous system physiology / MGI
- abnormal response/metabolism to endogenous compounds / MGI
- increased susceptibility to experimental autoimmune encephalomyelitis / MGI
- decreased susceptibility to experimental autoimmune encephalomyelitis / MGI
- decreased susceptibility to autoimmune diabetes / MGI
- increased susceptibility to parasitic infection / MGI
- increased susceptibility to type I hypersensitivity reaction / MGI
- decreased Peyer's patch number / MGI
- abnormal follicular dendritic cell morphology / MGI
- absent follicular dendritic cells / MGI
- decreased IgG1 level / MGI
- increased circulating tumor necrosis factor level / MGI
- decreased circulating interleukin-6 level / MGI
- decreased circulating interleukin-1 beta level / MGI
- increased interleukin-6 secretion / MGI
- decreased interleukin-6 secretion / MGI
- abnormal chemokine secretion / MGI
- decreased susceptibility to endotoxin shock / MGI
- increased susceptibility to endotoxin shock / MGI
- decreased physiological sensitivity to xenobiotic / MGI
- increased sensitivity to induced cell death / MGI
- increased sensitivity to induced morbidity/mortality / MGI
- decreased sensitivity to induced morbidity/mortality / MGI
- decreased sensitivity to xenobiotic induced morbidity/mortality / MGI
- increased susceptibility to bacterial infection induced morbidity/mortality / MGI
- abnormal neuron proliferation / MGI
- abnormal oval cell physiology / MGI
- tumor regression / MGI
- impaired adaptive thermogenesis / MGI
- decreased susceptibility to dopaminergic neuron neurotoxicity / MGI
- decreased microglial cell number / MGI
- impaired humoral immune response / MGI
- impaired central nervous system regeneration / MGI
Information on how we integrate external resources can be found here
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