- 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
B6.DDD1-plt/Orl
Status | Available to order |
EMMA ID | EM:02423 |
Citation information | RRID:IMSR_EM:02423 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.DDD1-plt/Orl |
Alternative name | paucity of lymph node T cells (plt) |
Strain type | Spontaneous |
Allele/Transgene symbol | plt |
Gene/Transgene symbol | plt |
Information from provider
Provider | Hideki Nakano |
Provider affiliation | National Institute of Environmental Health Science |
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 mice were backcrossed to C57BL/6 mice for 10 generations in Toho University, Japan; plt mice on C57BL/6 background have been maintained by inbreeding. |
References |
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Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Disease and phenotype information
MGI allele-associated human disease models
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
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