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Protein Coding Gene : Prdx5 peroxiredoxin 5

Primary Identifier  MGI:1859821 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  54683
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables thioredoxin-dependent peroxiredoxin activity. Predicted to be involved in several processes, including NADPH oxidation; cell redox homeostasis; and regulation of apoptotic process. Located in mitochondrion. Is expressed in several structures, including central nervous system; genitourinary system; retina; salivary gland; and spleen. Orthologous to human PRDX5 (peroxiredoxin 5).
PHENOTYPE: Mice homozygous for a null allele show increased susceptibility to high fat diet-induced obesity and hepatic steatosis. Mice homozygous for a different null allele show elevated nitric oxide production and oxidative stress in bone-marrow-derived dendritic cells. [provided by MGI curators]
  • synonyms:
  • PrxV,
  • peroxisomal membrane protein 20,
  • AOEB166,
  • peroxiredoxin V,
  • MGI:1349456,
  • PMP20,
  • Prdx6,
  • peroxiredoxin 5,
  • Pmp20,
  • Prdx5,
  • AOPP

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

9 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

 

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0 Driver For