# ALG6, alpha-1,3-glucosyltransferase

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21173423](https://www.wikidata.org/wiki/Q21173423)  
**Source**: https://4ort.xyz/entity/alg6-alpha-1-3-glucosyltransferase


## References

1. UniProt
2. Q20641742
3. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9Y672)
4. [A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9Y672)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9Y672&geneProductId=UniProtKB:Q9Y672)
6. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9Y672)
7. [Defining the membrane proteome of NK cells](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9Y672&geneProductId=UniProtKB:Q9Y672)
8. [Defining the membrane proteome of NK cells](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9Y672)
9. [Analysis of multiple mutations in the hALG6 gene in a patient with congenital disorder of glycosylation Ic](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9Y672&geneProductId=UniProtKB:Q9Y672)
10. [Analysis of multiple mutations in the hALG6 gene in a patient with congenital disorder of glycosylation Ic](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9Y672)
11. ensembl Release 93