Gene Ontology annotation through association of InterPro records with GO terms

Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity

Annotation inferences using phylogenetic trees

Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt

Combined Automated Annotation using Multiple IEA Methods

Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik.

Defining the membrane proteome of NK cells.

ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients.

Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein

Addition of the first mannose to the N-glycan precursor by ALG1

Defective ALG1 does not transfer the first Man to the N-glycan precursor

UniProtKB Q9BT22 (ALG1_HUMAN) curated record

Topological and enzymatic analysis of human Alg2 mannosyltransferase reveals its role in lipid-linked oligosaccharide biosynthetic pathway.

Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik.

Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I.

[Prokaryotic expression of human Alg1 protein and analysis of the transmembrane domain properties].