- enlarged spleen / MGI
- enlarged lymph nodes / MGI
- decreased body weight / MGI
- dehydration / MGI
- hunched posture / MGI
- anemia / MGI
- abnormal seizure response to electrical stimulation / MGI
- edema / MGI
- increased inflammatory response / MGI
- kidney inflammation / MGI
- liver inflammation / MGI
- lung inflammation / MGI
- vasculitis / MGI
- pancreas inflammation / MGI
- salivary gland inflammation / MGI
- premature death / MGI
- abnormal hypersensitivity reaction / MGI
- no abnormal phenotype detected / MGI
- maximal tonic hindlimb extension seizures / MGI
- abnormal mast cell physiology / MGI
- increased immunoglobulin level / MGI
- increased IgG level / MGI
- increased IgM level / MGI
- increased IgA level / MGI
- glomerulonephritis / MGI
- increased urine protein level / MGI
- increased susceptibility to induced arthritis / MGI
- tonic-clonic seizures / MGI
- increased anti-double stranded DNA antibody level / MGI
- increased anti-chromatin antibody level / MGI
- decreased susceptibility to parasitic infection / MGI
- skeleton phenotype / MGI
- increased susceptibility to type I hypersensitivity reaction / MGI
- increased germinal center B cell number / MGI
- increased IgG1 level / MGI
- increased IgG2a level / MGI
- increased IgG2b level / MGI
- increased IgG3 level / MGI
- decreased B cell apoptosis / MGI
- mortality/aging / MGI
- renal glomerular protein deposits / MGI
NOD.B6-(D1Mit15-D1Mit359)/GhjCnrm
Status | Available to order |
EMMA ID | EM:01396 |
Citation information | RRID:IMSR_EM:01396 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 | NOD.B6-(D1Mit15-D1Mit359)/GhjCnrm |
Alternative name | NOD.B6-C1D(L2) |
Strain type | Spontaneous |
Allele/Transgene symbol | Nktcn1C57BL/6J, Fcgr2b |
Gene/Transgene symbol | Nktcn1, Fcgr2b |
Information from provider
Provider | Henri-Jean Garchon |
Provider affiliation | ER70 CNRS et Unite 125 Inserm |
Genetic information | NOD congenic strain with the distal chromosome 1 from C57BL/6 (line 2). |
Phenotypic information | This line bears the main QTL controlling serum levels of IgG1 and IgG2b in NOD mice. The main candidate is the Fcgr2 gene that codes for the low affinity type 2 receptor for IgG, whose expression is decreased by 90% in macrophages. This same interval also controls the severity of experimental arthritis, the number and the function of natural killer T cells, IgE serum levels, and an increased resistance to endotoxin shock. |
Breeding history | 20 generations of backcrosses followed by sister-brother matings. Selection of subcongenics by additional backcrosses. |
References | None available |
Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
MGI phenotypes (gene matching)
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