MOGS

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Results for "MOGS": 1 gene, 5 gene sets

Name
MOGS Gene mannosyl-oligosaccharide glucosidase This gene encodes the first enzyme in the N-linked oligosaccharide processing pathway. The enzyme cleaves the distal alpha-1,2-linked glucose residue from the Glc(3)-Man(9)-GlcNAc(2) oligosaccharide precursor. This protein is located in the lumen of the endoplasmic reticulum. Defects in this gene are a cause of type IIb congenital disorder of glycosylation (CDGIIb). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]
MOGS Gene Set From Pathway Commons Protein-Protein Interactions interacting proteins for MOGS from the Pathway Commons Protein-Protein Interactions dataset.
MOGS Gene Set From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the MOGS gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.
Defective MOGS causes MOGS-CDG (CDG-2b) Gene Set From Reactome Pathways 2014 proteins participating in the Defective MOGS causes MOGS-CDG (CDG-2b) pathway from the Reactome Pathways dataset.
Defective MOGS causes CDG-2b Gene Set From Reactome Pathways 2024 proteins participating in the Defective MOGS causes CDG-2b pathway from the Reactome Pathways 2024 dataset.
MOGS-congenital disorder of glycosylation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MOGS-congenital disorder of glycosylation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.