# peroxisomal biogenesis factor 7

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21122478](https://www.wikidata.org/wiki/Q21122478)  
**Source**: https://4ort.xyz/entity/peroxisomal-biogenesis-factor-7-q21122478


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/O00628)
3. Q20641742
4. [Functional studies on human Pex7p: subcellular localization and interaction with proteins containing a peroxisome-targeting signal type 2 and other peroxins](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00628&geneProductId=UniProtKB:O00628)
5. [Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00628&geneProductId=UniProtKB:O00628)
6. [Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00628&geneProductId=UniProtKB:O00628)
7. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00628&geneProductId=UniProtKB:O00628)
8. [Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00628&geneProductId=UniProtKB:O00628)
9. [Identification and characterization of the human orthologue of yeast Pex14p](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00628&geneProductId=UniProtKB:O00628)
10. [Identification of PEX7 as the second gene involved in Refsum disease](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00628&geneProductId=UniProtKB:O00628)
11. Ensembl Release 99
12. UMLS 2023
13. Transporter Classification database