MOGS

Gene Name		mannosyl-oligosaccharide glucosidase
Image		No pdb structure
Gene Ontology Annotations	Cellular Component	Endoplasmic Reticulum Endoplasmic Reticulum Membrane Membrane Integral Component Of Membrane Extracellular Vesicular Exosome
	Molecular Function	Mannosyl-oligosaccharide Glucosidase Activity Glucosidase Activity
	Biological Process	Protein Folding Protein N-linked Glycosylation Oligosaccharide Metabolic Process Protein N-linked Glycosylation Via Asparagine Post-translational Protein Modification Cellular Protein Metabolic Process
Pathways		Defective ALG2 causes ALG2-CDG (CDG-1i) Diseases of glycosylation Post-translational protein modification Defective ALG3 causes ALG3-CDG (CDG-1d) Defective DPAGT1 causes DPAGT1-CDG (CDG-1j) and CMSTA2 Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS) Defective ALG1 causes ALG1-CDG (CDG-1k) Defective MGAT2 causes MGAT2-CDG (CDG-2a) Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) Defective RFT1 causes RFT1-CDG (CDG-1n) Defective MOGS causes MOGS-CDG (CDG-2b) Defective ALG6 causes ALG6-CDG (CDG-1c) Asparagine N-linked glycosylation Defective ALG8 causes ALG8-CDG (CDG-1h) Defective ALG9 causes ALG9-CDG (CDG-1l) Defective MAN1B1 causes MRT15 Defective MPDU1 causes MPDU1-CDG (CDG-1f) Defective ALG12 causes ALG12-CDG (CDG-1g) N-glycan trimming in the ER and Calnexin/Calreticulin cycle Diseases associated with N-glycosylation of proteins Defective ALG11 causes ALG11-CDG (CDG-1p)
Drugs
Diseases
GWAS
Protein-protein Interactions		1 interactors: CHGB
Entrez ID		7841
HPRD ID		03214
Ensembl ID		ENSG00000115275
Uniprot IDs		Q13724 Q58F09
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?		antiviral april broad compromises diathesis endoplasmic england entry enveloped genetically glucosidase glucosidases glycan hypogammaglobulinemia infectious issue journal manifested mannosyl oligosaccharide paradox phenomenon reticulum sadat spectrum unambiguously validates valuable viruses