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PEX10

peroxisomal biogenesis factor 10

PEX10 is a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms.

Gene Name:	peroxisomal biogenesis factor 10
Synonyms:	PEX10, NALD, PBD6A, PBD6B, Peroxin 10, Peroxisome assembly protein 10, Peroxin-10, RING finger protein 69, RNF69
Target Sequences:	NM_002617 NP_002608.1 O60683

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For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).

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