# Peroxisomal biogenesis factor 10

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21125810](https://www.wikidata.org/wiki/Q21125810)  
**Source**: https://4ort.xyz/entity/peroxisomal-biogenesis-factor-10-q21125810


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/O60683)
3. Q20641742
4. [Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients](http://www.ebi.ac.uk/QuickGO/annotations?protein=O60683&geneProductId=UniProtKB:O60683)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=O60683&geneProductId=UniProtKB:O60683)
6. [PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import](http://www.ebi.ac.uk/QuickGO/annotations?protein=O60683&geneProductId=UniProtKB:O60683)
7. [Molecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10p](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60683)
8. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60683)
9. [Peroxisome synthesis in the absence of preexisting peroxisomes](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60683)
10. [Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B](http://www.ebi.ac.uk/QuickGO/annotations?protein=O60683&geneProductId=UniProtKB:O60683)
11. [PEX14 is required for microtubule-based peroxisome motility in human cells](http://www.ebi.ac.uk/QuickGO/annotations?protein=O60683&geneProductId=UniProtKB:O60683)
12. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60683)
13. [Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60683)
14. [Identification of PEX10, the Gene Defective in Complementation Group 7 of the Peroxisome-Biogenesis Disorders](http://www.ebi.ac.uk/QuickGO/annotations?protein=O60683&geneProductId=UniProtKB:O60683)
15. [Identification of PEX10, the Gene Defective in Complementation Group 7 of the Peroxisome-Biogenesis Disorders](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60683)
16. Ensembl Release 99
17. Transporter Classification database