CD1.129-Ccr6tm1Gma/Cnbc
| Status | Available to order |
| EMMA ID | EM:06068 |
| Citation information | RRID:IMSR_EM:06068 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 | CD1.129-Ccr6tm1Gma/Cnbc |
| Alternative name | CD1.129-Ccr6 tm1/Gma |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Ccr6tm1Gma |
| Gene/Transgene symbol | Ccr6 |
Information from provider
| Provider | Rosa Varona |
| Provider affiliation | Centro Nacional de Biotecnologia (CNB-CSIC) |
| Genetic information | A PGK-neomycin resistance cassette replaced most of the coding exon, leaving the sequences that encode the 25 carboxy terminal amino acids. Northern analysis of spleen and thymus did not detect mRNA in homozygous mutant mice. Mutant mice backcrossed to CD1 more than 9 generations. |
| Phenotypic information | Ccr6-deficient mice have underdeveloped Peyer's patches, impaired leukocyte homeostasis and altered contact hypersensitivity and delayed-type hypersensitivity responses. |
| Breeding history | The original mutant strain was backcrossed to CD1 genetic background more than 9 generations. |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | yes |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
| Animals used for archiving | homozygous CD-1 outbred stock (syn.: outbr. CD-1 or CD1, Swiss CD-1 or CD1, ICR(CD-1), etc.) males, wild-type CD-1 outbred stock (syn.: outbr. CD-1 or CD1, Swiss CD-1 or CD1, ICR(CD-1), etc.) females |
| Stage of embryos | 4/8-cell |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (allele matching)
- increased leukocyte cell number / MGI
- decreased leukocyte cell number / MGI
- abnormal Peyer's patch morphology / MGI
- decreased inflammatory response / MGI
- abnormal Peyer's patch follicle morphology / MGI
- abnormal CD4-positive, alpha-beta T cell physiology / MGI
- abnormal myeloid dendritic cell morphology / MGI
MGI phenotypes (gene matching)
- increased leukocyte cell number / MGI
- decreased leukocyte cell number / MGI
- abnormal Peyer's patch morphology / MGI
- abnormal choroid plexus morphology / MGI
- decreased IgA level / MGI
- increased activated T cell number / MGI
- decreased inflammatory response / MGI
- no abnormal phenotype detected / MGI
- abnormal dendritic cell physiology / MGI
- abnormal gut-associated lymphoid tissue morphology / MGI
- abnormal Peyer's patch follicle morphology / MGI
- abnormal Peyer's patch germinal center morphology / MGI
- abnormal Peyer's patch T cell area morphology / MGI
- decreased susceptibility to bacterial infection / MGI
- increased susceptibility to viral infection / MGI
- abnormal CD4-positive, alpha beta T cell morphology / MGI
- abnormal T cell physiology / MGI
- abnormal macrophage physiology / MGI
- abnormal B cell physiology / MGI
- decreased IgE level / MGI
- increased IgM level / MGI
- abnormal lymphocyte morphology / MGI
- decreased susceptibility to experimental autoimmune encephalomyelitis / MGI
- increased B-1 B cell number / MGI
- increased T cell number / MGI
- decreased B cell number / MGI
- increased double-positive T cell number / MGI
- increased T cell proliferation / MGI
- abnormal CD4-positive, alpha-beta T cell physiology / MGI
- decreased susceptibility to type I hypersensitivity reaction / MGI
- abnormal myeloid dendritic cell morphology / MGI
- decreased CD4-positive, alpha beta T cell number / MGI
- decreased CD8-positive, alpha-beta T cell number / MGI
- decreased Peyer's patch number / MGI
- abnormal follicular dendritic cell physiology / MGI
- abnormal follicular dendritic cell antigen presentation / MGI
- abnormal peritoneal macrophage morphology / MGI
- abnormal alpha-beta intraepithelial T cell morphology / MGI
- abnormal CD4-positive, alpha-beta intraepithelial T cell morphology / MGI
- abnormal CD8 positive, alpha-beta intraepithelial T cell morphology / MGI
- decreased IgG3 level / MGI
- decreased tumor necrosis factor secretion / MGI
- increased interferon-gamma secretion / MGI
- abnormal interleukin secretion / MGI
- decreased interleukin-10 secretion / MGI
- decreased interleukin-12 secretion / MGI
- decreased interleukin-4 secretion / MGI
- decreased interleukin-5 secretion / MGI
- impaired eosinophil recruitment / MGI
- abnormal intraepithelial T cell number / MGI
- decreased macrophage nitric oxide production / MGI
- decreased macrophage cytokine production / MGI
Literature references
- CCR6-deficient mice have impaired leukocyte homeostasis and altered contact hypersensitivity and delayed-type hypersensitivity responses.;Varona R, Villares R, Carramolino L, Goya I, Zaballos A, Gutiérrez J, Torres M, Martínez-A C, Márquez G, ;2001;The Journal of clinical investigation;107;R37-45; 11254677
- CCR6 has a non-redundant role in the development of inflammatory bowel disease.;Varona Rosa, Cadenas Vanesa, Flores Juana, Martínez-A Carlos, Márquez Gabriel, ;2003;European journal of immunology;33;2937-46; 14515278
- CCR6 regulates CD4+ T-cell-mediated acute graft-versus-host disease responses.;Varona Rosa, Cadenas Vanesa, Gómez Lucio, Martínez-A Carlos, Márquez Gabriel, ;2005;Blood;106;18-26; 15774622
- CCR6 regulates the function of alloreactive and regulatory CD4+ T cells during acute graft-versus-host disease.;Varona Rosa, Cadenas Vanesa, Lozano María, Moreno-Ortiz Maria Carmen, Kremer Leonor, Martínez-A Carlos, Márquez Gabriel, ;2006;Leukemia & lymphoma;47;1469-76; 16966255
- Protective immunity and delayed type hypersensitivity reaction are uncoupled in experimental Leishmania major infection of CCR6-negative mice.;Lechner Anja, Ritter Uwe, Varona Rosa, Marquez Gabriel, Bogdan Christian, Körner Heinrich, ;2007;Microbes and infection;9;291-9; 17317260
- CCR6 regulates EAE pathogenesis by controlling regulatory CD4+ T-cell recruitment to target tissues.;Villares Ricardo, Cadenas Vanessa, Lozano María, Almonacid Luis, Zaballos Angel, Martínez-A Carlos, Varona Rosa, ;2009;European journal of immunology;39;1671-81; 19499521
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).
