- altered response to myocardial infarction / MGI
- abnormal leukocyte adhesion / MGI
- abnormal cellular extravasation / MGI
- decreased mast cell number / MGI
- decreased susceptibility to type III hypersensitivity reaction / MGI
- abnormal Kupffer cell morphology / MGI
- impaired hematopoiesis / MGI
- abnormal neutrophil physiology / MGI
- granulomatous inflammation / MGI
- increased susceptibility to parasitic infection / MGI
- immune system phenotype / MGI
- increased susceptibility to fungal infection / MGI
B6.129S4-Ccr1tm1Gao/Biat
Status | Available to order |
EMMA ID | EM:11144 |
Citation information | RRID:IMSR_EM:11144 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 | B6.129S4-Ccr1tm1Gao/Biat |
Alternative name | 1-B |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Ccr1tm1Gao |
Gene/Transgene symbol | Ccr1 |
Information from provider
Provider | Bruno Luckow |
Provider affiliation | Nephrologisches Zentrum, Arbeitsgruppe Klinische Biochemie, Klinikum der Universitaet Muenchen, Medizinische Klinik und Poliklinik IV |
Genetic information | The chemokine receptor Ccr1 has been inactivated by homologous recombination. |
Phenotypic information | Homozygous:Homozygous animals appear healthy and fertile and show unchallenged no obvious phenotype. Upregulated in many infectious and inflammatory diseases. Important role in leukocyte chemotaxis and innate immunity. Ccr1-deficient mice show accelerated mortality in an Aspergillus fumigatus infection model and suppression of acute and chronic cardiac allograft rejection. Phenotypic effects in hematopoiesis, host defense and inflammation.Heterozygous:Unknown, but most likely wild-type phenotype |
Breeding history | Initially backcrossed for 6 generations to C57BL/6J and then for other 9 generations to C57BL/6NCrl genetic background. N15+F2 |
References |
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Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | not known |
Information from EMMA
Archiving centre | University of Veterinary Medicine, Vienna, Austria |
Animals used for archiving | homozygous Other (please specify below) males |
Disease and phenotype information
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- decreased mast cell number / MGI
- altered response to myocardial infarction / MGI
- impaired hematopoiesis / MGI
- lung inflammation / MGI
- decreased airway responsiveness / MGI
- decreased susceptibility to viral infection / MGI
- decreased susceptibility to bacterial infection / MGI
- abnormal macrophage physiology / MGI
- abnormal neutrophil physiology / MGI
- granulomatous inflammation / MGI
- glomerulonephritis / MGI
- increased urine protein level / MGI
- abnormal leukocyte adhesion / MGI
- increased length of allograft survival / MGI
- decreased susceptibility to experimental autoimmune encephalomyelitis / MGI
- increased susceptibility to parasitic infection / MGI
- glomerulosclerosis / MGI
- abnormal renal glomerulus morphology / MGI
- immune system phenotype / MGI
- increased susceptibility to fungal infection / MGI
- increased blood urea nitrogen level / MGI
- decreased susceptibility to type III hypersensitivity reaction / MGI
- increased susceptibility to type IV hypersensitivity reaction / MGI
- decreased CD4-positive, alpha beta T cell number / MGI
- decreased CD8-positive, alpha-beta T cell number / MGI
- abnormal Kupffer cell morphology / MGI
- increased IgG2a level / MGI
- increased tumor necrosis factor secretion / MGI
- decreased tumor necrosis factor secretion / MGI
- increased interferon-gamma secretion / MGI
- decreased circulating interferon-gamma level / MGI
- decreased interleukin-10 secretion / MGI
- increased interleukin-12 secretion / MGI
- decreased interleukin-13 secretion / MGI
- impaired neutrophil recruitment / MGI
- abnormal chemokine secretion / MGI
- cecum inflammation / MGI
- decreased susceptibility to bacterial infection induced morbidity/mortality / MGI
- abnormal cellular extravasation / MGI
- abnormal circulating chemokine level / MGI
- increased macrophage nitric oxide production / MGI
- glomerular crescent / MGI
Literature references
- Impaired host defense, hematopoiesis, granulomatous inflammation and type 1-type 2 cytokine balance in mice lacking CC chemokine receptor 1.;Gao J L, Wynn T A, Chang Y, Lee E J, Broxmeyer H E, Cooper S, Tiffany H L, Westphal H, Kwon-Chung J, Murphy P M, ;1997;The Journal of experimental medicine;185;1959-68; 9166425
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