MGAT3: Mannosyl (Alpha-1,3-)-Glycoprotein Beta-1,4-N-Acetylglucosaminyltransferase

Key enzyme in the biosynthesis of hybrid and complex N-glycans, involved in cell adhesion and cancer progression.

Gene Information Card

Symbol MGAT3
Full Name Mannosyl (Alpha-1,3-)-Glycoprotein Beta-1,4-N-Acetylglucosaminyltransferase
Gene Type protein-coding
Chromosomal Location 22q13.1
NCBI Gene ID 4248 ncbi.nlm.nih.gov/gene/4248
Ensembl ID ENSG00000128272
UniProt ID Q09327
OMIM ID 604034
HGNC ID 7046
Aliases GNT-III, GNT3, GnT-III

Description

The MGAT3 gene encodes beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase (GnT-III), a Golgi enzyme that catalyzes the addition of a bisecting N-acetylglucosamine (GlcNAc) residue to the core mannose of N-glycans. This modification alters glycan conformation and modulates the function of glycoproteins involved in cell adhesion, migration, and signaling. MGAT3 expression is frequently altered in cancer and inflammatory diseases.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Hepatocellular carcinoma Reduced MGAT3 expression leads to altered N-glycosylation of E-cadherin, promoting cell migration and invasion. PMID: 23454750
Colorectal cancer Loss of bisecting GlcNAc due to MGAT3 downregulation correlates with increased metastasis and poor prognosis. PMID: 25670082
Breast cancer MGAT3 overexpression suppresses tumor growth by modifying EGFR glycosylation and signaling. PMID: 21145416
Rheumatoid arthritis MGAT3 expression is upregulated in synovial fibroblasts, affecting integrin-mediated adhesion. PMID: 17374726

Expression Profile

Tissue Expression
Tissue nTPM level
Liver 5.2 Medium
Kidney 3.8 Low
Brain 2.1 Low
Placenta 6.7 Medium
Lung 1.5 Not detected
Cell Line Expression
Cell Line nTPM Notes
HepG2 4.9 Hepatocellular carcinoma cell line
MCF7 3.2 Breast cancer cell line
A549 1.8 Lung carcinoma cell line
HEK293 2.5 Embryonic kidney cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1A>G (p.Met1?) Missense <0.01% Loss of start codon; likely loss of function
c.104C>T (p.Pro35Leu) Missense <0.01% Unknown functional effect
c.682G>A (p.Gly228Arg) Missense <0.01% Reported in COSMIC; potential impact on enzyme activity
Mutation functional classification

Loss of Function (LOF)

Mutations that abolish start codon or disrupt catalytic domain are predicted to reduce or eliminate GnT-III activity, leading to altered N-glycan profiles.

Gain of Function (GOF)

No documented gain-of-function mutations in MGAT3.

Dominant Negative (DN)

No evidence of dominant-negative effects for MGAT3 mutations.

Pathways

N-Glycan biosynthesis (KEGG: hsa00510)
Biosynthesis of N-glycan antennae (Reactome: R-HSA-975578)

Protein Summary

GnT-III is a type II transmembrane glycoprotein localized to the Golgi apparatus. It transfers N-acetylglucosamine from UDP-GlcNAc to the beta-linked mannose of the N-glycan core, creating a bisecting GlcNAc structure. This modification inhibits further processing by other glycosyltransferases, thereby regulating the branching and complexity of N-glycans. GnT-III plays a critical role in cell-cell adhesion, receptor signaling, and cancer metastasis.

Related Products

Product name Cat.No. Species Gene ID
MGAT3 Knockout HEK293 Cell Line EDJ-KQ5207 Human 4248 Details Get a Quote
MGAT3 Knockout HeLa Cell Line EDJ-KQ53869 Human 4248 Details Get a Quote
MGAT3 Knockout A-549 Cell Line EDJ-KQ62357 Human 4248 Details Get a Quote
MGAT3 Knockout HCT 116 Cell Line EDJ-KQ70827 Human 4248 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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