ALG2

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Results for "ALG2": 1 gene, 7 gene sets

Name
ALG2 Gene ALG2, alpha-1,3/1,6-mannosyltransferase This gene encodes a member of the glycosyltransferase 1 family. The encoded protein acts as an alpha 1,3 mannosyltransferase, mannosylating Man(2)GlcNAc(2)-dolichol diphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to form Man(3)GlcNAc(2)-dolichol diphosphate. Defects in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ii). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]
alg2 Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term alg2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
ALG2 Gene Set From Pathway Commons Protein-Protein Interactions interacting proteins for ALG2 from the Pathway Commons Protein-Protein Interactions dataset.
ALG2 Gene Set From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the ALG2 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.
Defective ALG2 causes ALG2-CDG (CDG-1i) Gene Set From Reactome Pathways 2014 proteins participating in the Defective ALG2 causes ALG2-CDG (CDG-1i) pathway from the Reactome Pathways dataset.
Alpha-1,3/1,6-mannosyltransferase ALG2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Alpha-1,3/1,6-mannosyltransferase ALG2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Defective ALG2 causes CDG-1i Gene Set From Reactome Pathways 2024 proteins participating in the Defective ALG2 causes CDG-1i pathway from the Reactome Pathways 2024 dataset.
ALG2-congenital disorder of glycosylation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ALG2-congenital disorder of glycosylation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.