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Heritable Phenotypic Marker : plt paucity of lymph node T cells

Primary Identifier	MGI:3664332	Organism	mouse, laboratory
Chromosome	4	Mgi Type	heritable phenotypic marker

description

FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Used to study Sjogren's syndrome.
PHENOTYPE: In homozygous mutant mice, naive T cells fail to localize in the lymph nodes or in the lymphoid regions of the spleen. [provided by MGI curators]

synonyms:
paucity of lymph node T cells,
plt

earliestPublication:
Nakano H, et al. (1993) 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 23(10):2434-9

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

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Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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