plt
Spontaneous Allele Detail

Summary

• 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

Mutation origin

• Strain of Origin: DDD/1

Mutation description

• Allele Type: Spontaneous
• Mutation: Intergenic deletion
• plt involves 2 genes/genome features (Ccl19, Ccl21a) View all
• Mutation details: This 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

Disease models

Expression

In Structures Affected by this Mutation:

14 anatomical structure(s)

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

References

• 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: 79 reference(s)