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Spontaneous Allele Detail
Symbol: plt
Name: paucity of lymph node T cells; paucity of lymph node T-cells
MGI ID: MGI:1857881
Gene: plt  Location: unknown  Genetic Position: Chr4, Syntenic
Alliance: plt page
Strain of Origin:  DDD/1
Allele Type:    Spontaneous
Mutation:    Intergenic deletion
  plt involves 2 genes/genome features (Ccl19, Ccl21a) View all
Mutation detailsThis mutation is a deletion region on chromosome 4 which includes the Ccl19 and Ccl21a genes (see also revised nomenclature for the Ccl21 family of genes). (J:58157, J:65808, J:66381, J:93716)
Inheritance:    Recessive
View phenotypes and curated references for all genotypes (concatenated display).
Disease models
In Structures Affected by this Mutation: 14 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 4 strains available      Cell Lines: 0 lines available
Carrying any plt Mutation:  4 strains or lines available
Original:  J:15290 Nakano H, et al., Nonspecific augmentation of lymph node T cells and I-E-independent selective deletion of V beta 14+ T cells by Mtv-2 in the DDD mouse. Eur J Immunol. 1993 Oct;23(10):2434-9
All:  78 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory