MAN2A2

Gene Name		mannosidase, alpha, class 2A, member 2
Image		No pdb structure
Gene Ontology Annotations	Cellular Component	Golgi Membrane Integral Component Of Membrane
	Molecular Function	Mannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase Activity Zinc Ion Binding Hydrolase Activity, Hydrolyzing N-glycosyl Compounds Carbohydrate Binding
	Biological Process	Mannose Metabolic Process Protein N-linked Glycosylation Via Asparagine Post-translational Protein Modification Cellular Protein Metabolic Process
Pathways		Diseases of glycosylation Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS) Transport to the Golgi and subsequent modification Defective ALG1 causes ALG1-CDG (CDG-1k) Defective MGAT2 causes MGAT2-CDG (CDG-2a) Defective MOGS causes MOGS-CDG (CDG-2b) N-glycan antennae elongation in the medial/trans-Golgi Defective ALG9 causes ALG9-CDG (CDG-1l) Defective MAN1B1 causes MRT15 Defective ALG11 causes ALG11-CDG (CDG-1p) Defective ALG2 causes ALG2-CDG (CDG-1i) Defective ALG3 causes ALG3-CDG (CDG-1d) Post-translational protein modification Defective DPAGT1 causes DPAGT1-CDG (CDG-1j) and CMSTA2 Reactions specific to the complex N-glycan synthesis pathway Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) Defective RFT1 causes RFT1-CDG (CDG-1n) Defective ALG6 causes ALG6-CDG (CDG-1c) Asparagine N-linked glycosylation Defective ALG8 causes ALG8-CDG (CDG-1h) Defective MPDU1 causes MPDU1-CDG (CDG-1f) Defective ALG12 causes ALG12-CDG (CDG-1g) Diseases associated with N-glycosylation of proteins
Drugs
Diseases
GWAS		Attention deficit hyperactivity disorder ( 18839057)
Protein-protein Interactions		5 interactors: CHD3 GIT1 IKBKAP LUC7L2 VIM
Entrez ID		4122
HPRD ID		02994
Ensembl ID		ENSG00000196547
Uniprot IDs		P49641 Q9P1E4
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?