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Protein Coding Gene : Pex6 peroxisomal biogenesis factor 6
Primary Identifier  MGI:2385054 Organism  mouse, laboratory
Chromosome  17 NCBI Gene Number  224824
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable several functions, including ATP binding activity; ATP hydrolysis activity; and ubiquitin-modified protein reader activity. Predicted to be involved in establishment of protein localization to peroxisome; protein stabilization; and protein unfolding. Located in photoreceptor cell cilium. Is expressed in brain; embryo; liver; and metanephros. Human ortholog(s) of this gene implicated in Heimler syndrome 2; Peroxisome biogenesis disorder 4B; and peroxisome biogenesis disorder 4A. Orthologous to human PEX6 (peroxisomal biogenesis factor 6).
  • synonyms:
  • MGI:2146801,
  • peroxisomal biogenesis factor 6,
  • RIKEN cDNA D130055I09 gene,
  • D130055I09Rik,
  • Pex6,
  • expressed sequence AI132582,
  • MGI:2445130,
  • AI132582,
  • MGC:6455
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Features --> Cross References

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

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

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Features --> Overlapping features

Proteins

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Interactions

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Gene --> Protein-Protein Interactions

Expression

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Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

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