Peroxin-7
{{Short description|Family of transport proteins}}
{{protein
|Name=peroxisomal biogenesis factor 7
|caption=
|image=
|width=
|HGNCid=8860
|Symbol=PEX7
|AltSymbols=
|EntrezGene=5191
|OMIM=601757
|RefSeq=NM_000288
|UniProt=O00628
|PDB=
|ECnumber=
|Chromosome=6
|Arm=q
|Band=21
|LocusSupplementaryData=-q22.2
}}
Peroxin-7 is a receptor associated with Refsum's disease and rhizomelic chondrodysplasia punctata type 1.
See also
External links
- [https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=refsum GeneReviews/NCBI/NIH/UW entry on Refsum Disease]
- [https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=rcdp GeneReviews/NIH/NCBI/UW entry on Rhizomelic Chondrodysplasia Punctata Type 1]
- {{MeshName|PEX7+protein,+human}}
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