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Protein Coding Gene : Tsc22d3 TSC22 domain family, member 3

Primary Identifier  MGI:1196284 Organism  mouse, laboratory
Chromosome  X NCBI Gene Number  14605
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Acts upstream of or within negative regulation of activation-induced cell death of T cells and response to osmotic stress. Located in nucleus. Is expressed in several structures, including early conceptus; genitourinary system; nervous system; sensory organ; and viscerocranium. Orthologous to human TSC22D3 (TSC22 domain family member 3).
PHENOTYPE: Hemizygous null males show mild deficits in sodium handling, weight reduction, hyperinsulinemia, resistance to liver steatosis, and sterility associated with azoospermia, testis dysplasia, Leydig cell hyperplasia, male germ cell apoptosis, arrested meiosis, and high FSH and testosterone levels. [provided by MGI curators]
  • synonyms:
  • glucocorticoid-induced leucine zipper,
  • Gilz,
  • Tsc22d3,
  • delta sleep inducing peptide, immunoreactor,
  • TSC22 domain family, member 3,
  • Dsip1

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

0 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

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.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

0 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For