ST3GAL2: ST3 Beta-Galactoside Alpha-2,3-Sialyltransferase 2

A key enzyme in sialic acid transfer, involved in glycoprotein and glycolipid biosynthesis, with implications in cancer and immune function.

Gene Information Card

Symbol ST3GAL2
Full Name ST3 beta-galactoside alpha-2,3-sialyltransferase 2
Gene Type protein-coding
Chromosomal Location 16q22.1
NCBI Gene ID 6483 ncbi.nlm.nih.gov/gene/6483
Ensembl ID ENSG00000140987
UniProt ID Q16842
OMIM ID 604034
HGNC ID 10863
Aliases SIAT4B, ST3GalII, ST3GALII

Description

ST3GAL2 encodes a Golgi membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates via an alpha-2,3 linkage. This enzyme is involved in the biosynthesis of sialylated glycoproteins and glycolipids, which are critical for cell-cell interactions, immune recognition, and tumor progression. The gene is expressed in multiple tissues, with highest levels in brain, placenta, and testis.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Colorectal Cancer Altered sialylation of cell surface glycans promotes metastasis and immune evasion. ST3GAL2 overexpression is associated with poor prognosis. PMID: 25605274, COSMIC
Breast Cancer Increased ST3GAL2 expression correlates with tumor grade and lymph node metastasis. PMID: 23542377
Gastric Cancer Upregulation of ST3GAL2 enhances cell migration and invasion via altered glycosylation. PMID: 27323861
Hepatocellular Carcinoma ST3GAL2-mediated sialylation of beta1-integrin promotes cell adhesion and migration. PMID: 28411363

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 12.5 High
Placenta 10.2 High
Testis 9.8 High
Lung 6.1 Medium
Colon 5.3 Medium
Breast 4.7 Medium
Liver 2.1 Low
Cell Line Expression
Cell Line nTPM Notes
HEK293 8.4 High expression in embryonic kidney cells
HeLa 6.2 Moderate expression in cervical cancer cells
MCF7 5.9 Moderate expression in breast cancer cells
HCT116 7.1 High expression in colorectal cancer cells
A549 4.3 Low-moderate expression in lung cancer cells
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.104G>A (p.Arg35His) Missense <0.01% Unknown functional impact; rare population variant
c.511C>T (p.Arg171Trp) Missense <0.01% Predicted damaging by SIFT; potential loss of activity
c.832G>A (p.Gly278Ser) Missense <0.01% Located in catalytic domain; may reduce enzyme activity
Mutation functional classification

Loss of Function (LOF)

Rare missense variants (e.g., p.Arg171Trp, p.Gly278Ser) are predicted to reduce sialyltransferase activity, potentially altering glycan profiles.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported in literature or databases.

Dominant Negative (DN)

No evidence for dominant-negative effects; ST3GAL2 functions as a monomer.

Pathways

Glycosphingolipid biosynthesis - lacto and neolacto series (KEGG: hsa00601)
N-Glycan biosynthesis (KEGG: hsa00510)
Sialic acid metabolism (Reactome: R-HSA-4085001)

Protein Summary

ST3GAL2 is a type II transmembrane protein localized to the Golgi apparatus. It catalyzes the transfer of sialic acid to terminal galactose residues on glycoproteins and glycolipids, forming alpha-2,3 linkages. The protein contains a short N-terminal cytoplasmic tail, a transmembrane domain, and a large C-terminal catalytic domain facing the Golgi lumen. Its activity is essential for the synthesis of sialyl Lewis antigens and other sialylated structures involved in cell adhesion and signaling.

Related Products

Product name Cat.No. Species Gene ID
ST3GAL2 Knockout HEK293 Cell Line EDJ-KQ5751 Human 6483 Details Get a Quote
ST3GAL2 Knockout A-549 Cell Line EDJ-KQ29163 Human 6483 Details Get a Quote
ST3GAL2 Knockout HCT 116 Cell Line EDJ-KQ29164 Human 6483 Details Get a Quote
ST3GAL2 Knockout HeLa Cell Line EDJ-KQ29165 Human 6483 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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