- abnormal immune system morphology / MGI
- decreased T cell number / MGI
- immune system phenotype / MGI
- abnormal leukocyte cell number / MGI
- abnormal lacrimal gland morphology / MGI
- abnormal immune system physiology / MGI
- abnormal T cell activation / MGI
- increased inflammatory response / MGI
- salivary gland inflammation / MGI
- abnormal gland morphology / MGI
- abnormal lymph node T cell domain morphology / MGI
- abnormal spleen red pulp morphology / MGI
- abnormal spleen white pulp morphology / MGI
- abnormal thymus cortex morphology / MGI
- abnormal immune system organ morphology / MGI
- abnormal leukocyte migration / MGI
- abnormal parotid gland morphology / MGI
- abnormal submandibular gland morphology / MGI
- increased length of allograft survival / MGI
- increased T cell number / MGI
- decreased T cell number / MGI
- increased susceptibility to autoimmune disorder / MGI
- immune system phenotype / MGI
- increased memory T cell number / MGI
- decreased single-positive T cell number / MGI
- lymph node hypoplasia / MGI
- small Peyer's patches / MGI
- abnormal peripheral lymph node morphology / MGI
- abnormal physiological response to xenobiotic / MGI
- submandibular gland inflammation / MGI
- lacrimal gland inflammation / MGI
- parotid gland inflammation / MGI
- small thymus medulla / MGI
C.DDD1-plt/Orl
| Status | Available to order |
| EMMA ID | EM:02575 |
| Citation information | RRID:IMSR_EM:02575 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 | C.DDD1-plt/Orl |
| Alternative name | BALB/c-plt/plt |
| Strain type | Spontaneous |
| Allele/Transgene symbol | Ccl19, Ccl21a, plt |
| Gene/Transgene symbol | Ccl19, Ccl21a, plt |
Information from provider
| Provider | Hideki Nakano |
| Provider affiliation | National Institute of Environmental Health Science |
| Additional owner | Vanessa Larrigaldie maintains this strain. |
| Genetic information | CCL19 and CCL21a (also called CCL21-ser) genes are deleted. |
| Phenotypic information | Migration of CCR7+ leukocytes including T cells and dendritic cells from blood or peripheral tissues to lymphoid organs is severely impaired in plt/plt mice. |
| Breeding history | DDD/1-plt/plt was backcrossed to BALB/c for 10 generations. |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | yes |
Information from EMMA
| Archiving centre | CNRS-TAAM – Typing and Archiving of Animal Models, Orléans, France |
| Animals used for archiving | homozygous BALB/c males |
Disease and phenotype information
MGI phenotypes (gene matching)
Literature references
- Gene duplications at the chemokine locus on mouse chromosome 4: multiple strain-specific haplotypes and the deletion of secondary lymphoid-organ chemokine and EBI-1 ligand chemokine genes in the plt mutation.;Nakano H, Gunn M D, ;2001;Journal of immunology (Baltimore, Md. : 1950);166;361-9; 11123313
- A novel mutant gene involved in T-lymphocyte-specific homing into peripheral lymphoid organs on mouse chromosome 4.;Nakano H, Mori S, Yonekawa H, Nariuchi H, Matsuzawa A, Kakiuchi T, ;1998;Blood;91;2886-95; 9531599
- Mice lacking expression of secondary lymphoid organ chemokine have defects in lymphocyte homing and dendritic cell localization.;Gunn M D, Kyuwa S, Tam C, Kakiuchi T, Matsuzawa A, Williams L T, Nakano H, ;1999;The Journal of experimental medicine;189;451-60; 9927507
- Genetic defect in T lymphocyte-specific homing into peripheral lymph nodes.;Nakano H, Tamura T, Yoshimoto T, Yagita H, Miyasaka M, Butcher E C, Nariuchi H, Kakiuchi T, Matsuzawa A, ;1997;European journal of immunology;27;215-21; 9022021
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).
