SCUBA

MGAT5 — Alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase

MGAT5 belongs to a gene co-expression module in 5 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

MGAT5's module in each cell type

Cell typeModuleShares the module with
FibroblastsECM Glycan Remodeling
ECM remodeling
ATP1B1, CHST11, COL8A2, LIMCH1, MGAT4A, MMP11, MYO7A, NCALD +3 moreView in SCUBA
Lymphatic endothelialActin-based Migration
Cytoskeletal
AUTS2, GAS7, NHSL1, PAN3, PCCA, PPP6R3, TRIO, ZFPM2View in SCUBA
MacrophagesEndosomal Rab Trafficking
Vesicular traficking
ABL1, ANKS1A, ARB2A, CAMK1D, CPEB3, DENND4C, DISC1, FBXL17 +15 moreView in SCUBA
Mucosal-associated invariant T cellCytoskeletal Migration
migration & adhesion
CHST11, HDAC9, NCAM1, NCOA2, PITPNC1, RASA2, SSH2
NeutrophilsGeneral Homeostatic Regulation
Housekeeping
ARID2, EXOC4, FBXL17, LARP4B, MCU, RAD51B, RASA1

About the gene

SynonymsGNT-V, MGAT5A
Chromosome2: 134119983-134454621
Predicted locationMembrane
Essential geneNo
Protein classEnzymes, Metabolic proteins, Predicted membrane proteins
Molecular functionGlycosyltransferase, Transferase

Function

Catalyzes the addition of N-acetylglucosamine (GlcNAc) in beta 1-6 linkage to the alpha-linked mannose of biantennary N-linked oligosaccharides. Catalyzes an important step in the biosynthesis of branched, complex-type N-glycans, such as those found on EGFR, TGFR (TGF-beta receptor) and CDH2. Via its role in the biosynthesis of complex N-glycans, plays an important role in the activation of cellular signaling pathways, reorganization of the actin cytoskeleton, cell-cell adhesion and cell migration. MGAT5-dependent EGFR N-glycosylation enhances the interaction between EGFR and LGALS3 and thereby prevents rapid EGFR endocytosis and prolongs EGFR signaling. Required for efficient interaction between TGFB1 and its receptor. Enhances activation of intracellular signaling pathways by several types of growth factors, including FGF2, PDGF, IGF, TGFB1 and EGF. MGAT5-dependent CDH2 N-glycosylation inhibits CDH2-mediated homotypic cell-cell adhesion and contributes to the regulation of downstream signaling pathways. Promotes cell migration. Contributes to the regulation of the inflammatory response. MGAT5-dependent TCR N- glycosylation enhances the interaction between TCR and LGALS3, limits agonist-induced TCR clustering, and thereby dampens TCR-mediated responses to antigens. Required for normal leukocyte evasation and accumulation at sites of inflammation (By similarity). Inhibits attachment of monocytes to the vascular endothelium and subsequent monocyte diapedesis. [Secreted alpha-1,6-mannosylglycoprotein 6-beta-N- acetylglucosaminyltransferase A]: Promotes proliferation of umbilical vein endothelial cells and angiogenesis, at least in part by promoting the release of the growth factor FGF2 from the extracellular matrix

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.