Peroxin-7

Family of transport proteins
peroxisomal biogenesis factor 7
Identifiers
SymbolPEX7
NCBI gene5191
HGNC8860
OMIM601757
RefSeqNM_000288
UniProtO00628
Other data
LocusChr. 6 q21-q22.2
Search for
StructuresSwiss-model
DomainsInterPro

Peroxin-7 is a receptor associated with Refsum's disease and rhizomelic chondrodysplasia punctata type 1.

See also

  • Peroxin
  • GeneReviews/NCBI/NIH/UW entry on Refsum Disease
  • GeneReviews/NIH/NCBI/UW entry on Rhizomelic Chondrodysplasia Punctata Type 1
  • PEX7+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)


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