- decreased monocyte cell number / IMPC
- abnormal vibrissa morphology / IMPC
- improved glucose tolerance / IMPC
- increased circulating creatinine level / IMPC
- increased circulating amylase level / IMPC
- decreased circulating fructosamine level / IMPC
- increased bone mineral content / IMPC
- decreased KLRG1-positive NK cell number / IMPC
C57BL/6N-Atm1Brd Ifnar1tm2a(EUCOMM)Wtsi/WtsiOulu
Status | Available to order |
EMMA ID | EM:10181 |
International strain name | C57BL/6N-Atm1Brd Ifnar1tm2a(EUCOMM)Wtsi/WtsiOulu |
Alternative name | MEPD01000_2_C03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Ifnar1tm2a(EUCOMM)Wtsi |
Gene/Transgene symbol | Ifnar1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from EUCOMM ES clone MEPD01000_2_C03. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | University of Oulu, Oulu, Finland |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- improved glucose tolerance / IMPC
- decreased circulating fructosamine level / IMPC
- decreased monocyte cell number / IMPC
- decreased KLRG1-positive NK cell number / IMPC
- increased circulating creatinine level / IMPC
- abnormal vibrissa morphology / IMPC
- increased bone mineral content / IMPC
- increased circulating amylase level / IMPC
MGI phenotypes (gene matching)
- decreased bone mineral density / MGI
- increased leukocyte cell number / MGI
- altered susceptibility to infection / MGI
- abnormal inflammatory response / MGI
- increased incidence of induced tumors / MGI
- abnormal dendritic cell physiology / MGI
- increased susceptibility to viral infection / MGI
- abnormal macrophage physiology / MGI
- abnormal immunoglobulin level / MGI
- abnormal cytokine secretion / MGI
- no phenotypic analysis / MGI
- increased tumor growth/size / MGI
- abnormal CD8-positive, alpha-beta T cell physiology / MGI
- increased incidence of tumors by chemical induction / MGI
- abnormal osteoclast morphology / MGI
- abnormal response to infection / MGI
- impaired natural killer cell mediated cytotoxicity / MGI
- immune system phenotype / MGI
- corneal vascularization / MGI
- abnormal enzyme/coenzyme activity / MGI
- decreased NK cell number / MGI
- abnormal interferon-gamma secretion / MGI
- decreased tumor necrosis factor secretion / MGI
- decreased interferon-alpha secretion / MGI
- decreased interferon-beta secretion / MGI
- increased circulating interleukin-12 level / MGI
- decreased interleukin-6 secretion / MGI
- increased susceptibility to bacterial infection induced morbidity/mortality / MGI
- increased susceptibility to viral infection induced morbidity/mortality / MGI
- abnormal NK cell physiology / MGI
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