Caenorhabditis elegans
PRX-13
CELE_F32A5.6, F32A5.6
prx-13 is orthologous to the human gene PEX13 (OMIM:601789), which when mutated leads to Zellweger syndrome or neonatal adrenoleukodystrophy.
GO Process (2)
GO Function (0)
GO Component (0)
Gene Ontology Biological Process
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39528
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- Interactors 31
- Interactions 31
- Network