- 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 |
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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