- 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
- increased length of allograft survival / MGI
B6.Cg-Ccr1tm1Gao Ccr5tm1Blck/Biat
Status | Available to order |
EMMA ID | EM:11147 |
International strain name | B6.Cg-Ccr1tm1Gao Ccr5tm1Blck/Biat |
Alternative name | 15-B |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Ccr1tm1Gao, Ccr5tm1Blck |
Gene/Transgene symbol | Ccr1, Ccr5 |
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 receptors Ccr1 and Ccr5 have been inactivated by homologous recombination in ES cells and the resulting single knock-out mice have been crossed to generate the Ccr1/Ccr5 double knock-out mice. The Ccr1/Ccr5 double-deficient mice have been backcrossed to the C57BL/6NCrl genetic background. They contain a lacZ reporter gene at the inactivated Ccr5 locus. |
Phenotypic information | Homozygous:Homozygous animals appear healthy and fertile and if unchallenged show no obvious phenotype. So far only tested in a kidney transplantation experiment. Surprisingly, weaker phenotypic effects than both single knock-outs as if the 2 deficiencies would partially neutralize each other.Heterozygous:Unknown, but most likely wildtype phenotype. |
Breeding history | N14+F3 |
References |
|
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) |
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
- altered response to myocardial infarction / MGI
- abnormal locomotor behavior / MGI
- abnormal spatial learning / MGI
- abnormal cardiovascular system physiology / MGI
- decreased inflammatory response / MGI
- decreased susceptibility to viral infection / MGI
- increased susceptibility to bacterial infection / MGI
- abnormal CD4-positive, alpha beta T cell morphology / MGI
- abnormal leukocyte physiology / MGI
- abnormal conditioned taste aversion behavior / MGI
- abnormal cytokine secretion / MGI
- liver failure / MGI
- increased alcohol consumption / MGI
- abnormal leukocyte adhesion / MGI
- nervous system phenotype / MGI
- abnormal nervous system physiology / MGI
- abnormal glial cell physiology / MGI
- impaired macrophage chemotaxis / MGI
- increased length of allograft survival / MGI
- abnormal CD8-positive, alpha beta T cell morphology / MGI
- decreased T cell proliferation / MGI
- decreased susceptibility to injury / MGI
- cardiovascular system phenotype / MGI
- behavior/neurological phenotype / MGI
- reproductive system phenotype / MGI
- increased susceptibility to fungal infection / MGI
- abnormal heart size / MGI
- corneal vascularization / MGI
- increased susceptibility to type IV hypersensitivity reaction / MGI
- increased NK T cell number / MGI
- abnormal NK T cell physiology / MGI
- decreased NK cell number / MGI
- abnormal Kupffer cell morphology / MGI
- abnormal long term spatial reference memory / MGI
- increased IgG1 level / MGI
- decreased susceptibility to induced colitis / MGI
- increased interferon-gamma secretion / MGI
- decreased interleukin-1 beta secretion / MGI
- increased interleukin-4 secretion / MGI
- decreased interleukin-6 secretion / MGI
- abnormal cytokine level / MGI
- decreased susceptibility to endotoxin shock / MGI
- increased physiological sensitivity to xenobiotic / MGI
- abnormal astrocyte physiology / MGI
- abnormal Ito cell morphology / MGI
- abnormal cellular extravasation / MGI
- abnormal hepatocyte physiology / MGI
- decreased right ventricle systolic pressure / MGI
- mortality/aging / MGI
- increased fluid intake / MGI
- decreased microglial cell activation / 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
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).