Gene

prx-6

Species
Caenorhabditis elegans
Symbol
prx-6
Name
PeRoXisome assembly factor 6
Synonyms
  • CELE_F39G3.7
  • F39G3.7
Biotype
protein coding gene
Automated Description
Predicted to enable ATP hydrolysis activity. Involved in nematode larval development. Predicted to be located in cytoplasm and membrane. Predicted to be active in cytosol and peroxisomal membrane. Is expressed in hypodermis and intestine. 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).
WB Description
Predicted to enable ATP hydrolysis activity. Involved in nematode larval development. Predicted to be located in cytosol and peroxisomal membrane. Human ortholog(s) of this gene implicated in Heimler syndrome 2 and peroxisome biogenesis disorder 4A. Is an ortholog of human PEX6 (peroxisomal biogenesis factor 6).
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
None

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
WBcel235
Viewer Help
4.7155M4.7160M4.7165M4.7170M4.7175M4.7180M4.7185M4.7190M4.7195M4.7200M

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