Peroxin-7 is a receptor associated with Refsum's disease and rhizomelic chondrodysplasia punctata type 1.
| peroxisomal biogenesis factor 7 | |||||||
|---|---|---|---|---|---|---|---|
| Identifiers | |||||||
| Symbol | PEX7 | ||||||
| NCBI gene | 5191 | ||||||
| HGNC | 8860 | ||||||
| OMIM | 601757 | ||||||
| RefSeq | NM_000288 | ||||||
| UniProt | O00628 | ||||||
| Other data | |||||||
| Locus | Chr. 6 q21-q22.2 | ||||||
| |||||||
See also
editExternal links
edit- 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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