ALG3

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Results for "ALG3": 1 gene, 6 gene sets

Name
ALG3 Gene ALG3, alpha-1,3- mannosyltransferase This gene encodes a member of the ALG3 family. The encoded protein catalyses the addition of the first dol-P-Man derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]
ALG3 Gene Set From Pathway Commons Protein-Protein Interactions interacting proteins for ALG3 from the Pathway Commons Protein-Protein Interactions dataset.
ALG3 Gene Set From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the ALG3 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.
Defective ALG3 causes ALG3-CDG (CDG-1d) Gene Set From Reactome Pathways 2014 proteins participating in the Defective ALG3 causes ALG3-CDG (CDG-1d) pathway from the Reactome Pathways dataset.
Glycosyltransferase, ALG3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycosyltransferase, ALG3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Defective ALG3 causes CDG-1d Gene Set From Reactome Pathways 2024 proteins participating in the Defective ALG3 causes CDG-1d pathway from the Reactome Pathways 2024 dataset.
ALG3-congenital disorder of glycosylation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ALG3-congenital disorder of glycosylation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.