Peroxin-7
Family of transport proteins
peroxisomal biogenesis factor 7 | |||||||
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Identifiers | |||||||
Symbol | PEX7 | ||||||
NCBI gene | 5191 | ||||||
HGNC | 8860 | ||||||
OMIM | 601757 | ||||||
RefSeq | NM_000288 | ||||||
UniProt | O00628 | ||||||
Other data | |||||||
Locus | Chr. 6 q21-q22.2 | ||||||
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Peroxin-7 is a receptor associated with Refsum's disease and rhizomelic chondrodysplasia punctata type 1.
See also
- Peroxin
External links
- 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)
- v
- t
- e