# Protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21133271](https://www.wikidata.org/wiki/Q21133271)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/POMGNT1)  
**Source**: https://4ort.xyz/entity/protein-o-linked-mannose-n-acetylglucosaminyltransferase-1-beta-1-2--q21133271


## References

1. UniProt
2. Q20641742
3. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8WZA1)
4. [Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of alpha-dystroglycan](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8WZA1)
5. [A proteome-scale map of the human interactome network](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8WZA1)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8WZA1&geneProductId=UniProtKB:Q8WZA1)
7. [Cloning and expression of a novel UDP-GlcNAc:alpha-D-mannoside beta1,2-N-acetylglucosaminyltransferase homologous to UDP-GlcNAc:alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase I](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8WZA1&geneProductId=UniProtKB:Q8WZA1)
8. [Mutations in POMGNT1 cause non-syndromic retinitis pigmentosa](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8WZA1)
9. [Homozygosity Mapping and Whole-Genome Sequencing Links a Missense Mutation in POMGNT1 to Autosomal Recessive Retinitis Pigmentosa](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8WZA1)
10. [Carbohydrate-binding domain of the POMGnT1 stem region modulates O-mannosylation sites of α-dystroglycan](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8WZA1)
11. [Cloning and expression of a novel UDP-GlcNAc:alpha-D-mannoside beta1,2-N-acetylglucosaminyltransferase homologous to UDP-GlcNAc:alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase I](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8WZA1)
12. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8WZA1)
13. [Carbohydrate-binding domain of the POMGnT1 stem region modulates O-mannosylation sites of α-dystroglycan](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8WZA1&geneProductId=UniProtKB:Q8WZA1)
14. [Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of alpha-dystroglycan](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8WZA1&geneProductId=UniProtKB:Q8WZA1)
15. [Homozygosity Mapping and Whole-Genome Sequencing Links a Missense Mutation in POMGNT1 to Autosomal Recessive Retinitis Pigmentosa](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8WZA1&geneProductId=UniProtKB:Q8WZA1)
16. [Mutations in POMGNT1 cause non-syndromic retinitis pigmentosa](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8WZA1&geneProductId=UniProtKB:Q8WZA1)
17. [Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8WZA1&geneProductId=UniProtKB:Q8WZA1)
18. [Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8WZA1)
19. Ensembl Release 99