# Glucosidase, beta, acid

> mammalian protein found in Mus musculus

**Wikidata**: [Q14878772](https://www.wikidata.org/wiki/Q14878772)  
**Source**: https://4ort.xyz/entity/glucosidase-beta-acid


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/P17439)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=P17439&geneProductId=UniProtKB:P17439)
5. [Mitochondria and quality control defects in a mouse model of Gaucher disease--links to Parkinson's disease](http://www.ebi.ac.uk/QuickGO/annotations?protein=P17439&geneProductId=UniProtKB:P17439)
6. [Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies](http://www.ebi.ac.uk/QuickGO/annotations?protein=P17439&geneProductId=UniProtKB:P17439)
7. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P17439)
8. [LIMP-2 is a receptor for lysosomal mannose-6-phosphate-independent targeting of beta-glucocerebrosidase](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P17439)
9. [Mice lacking mannose 6-phosphate uncovering enzyme activity have a milder phenotype than mice deficient for N-acetylglucosamine-1-phosphotransferase activity](http://www.ebi.ac.uk/QuickGO/annotations?protein=P17439&geneProductId=UniProtKB:P17439)
10. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?protein=P17439&geneProductId=UniProtKB:P17439)
11. [Mice lacking mannose 6-phosphate uncovering enzyme activity have a milder phenotype than mice deficient for N-acetylglucosamine-1-phosphotransferase activity](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P17439)
12. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P17439)
13. [Mitochondria and quality control defects in a mouse model of Gaucher disease--links to Parkinson's disease](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P17439)
14. [Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P17439)
15. [Cholesterol glucosylation is catalyzed by transglucosylation reaction of β-glucosidase 1.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P17439)
16. [Cholesterol glucosylation is catalyzed by transglucosylation reaction of β-glucosidase 1.](http://www.ebi.ac.uk/QuickGO/annotations?protein=P17439&geneProductId=UniProtKB:P17439)
17. [Progranulin Recruits HSP70 to β-Glucocerebrosidase and Is Therapeutic Against Gaucher Disease](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P17439)
18. [LIMP-2 is a receptor for lysosomal mannose-6-phosphate-independent targeting of beta-glucocerebrosidase](http://www.ebi.ac.uk/QuickGO/annotations?protein=P17439&geneProductId=UniProtKB:P17439)
19. [Autophagic lysosome reformation dysfunction in glucocerebrosidase deficient cells: relevance to Parkinson disease](http://www.ebi.ac.uk/QuickGO/annotations?protein=P17439&geneProductId=UniProtKB:P17439)
20. [Autophagic lysosome reformation dysfunction in glucocerebrosidase deficient cells: relevance to Parkinson disease](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P17439)
21. ensembl Release 106