Gene

Pex6

Species
Drosophila melanogaster
Symbol
Pex6
Name
Peroxin 6
Synonyms
  • CG11919
  • CG30019
Biotype
protein coding gene
Automated Description
Predicted to enable ATP hydrolysis activity; protein transporter activity; and ubiquitin-modified protein reader activity. Involved in peroxisome organization. Located in peroxisome. Is expressed in embryonic cortex and yolk. 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).
FB Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR23077
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
Other Sources

Disease Associations

Cases where the expected disease association was NOT found
Cell color indicative of annotation volume

Transgenic Alleles

Models

Sequence Feature Viewer

Genome location
Assembly version
R6
Viewer Help
10.8800M10.8805M10.8810M10.8815M10.8820M10.8825M10.8830M

Sequence Details

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Expression

Primary Sources
Other Sources
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

Genetic Interactions