CHST13: Carbohydrate Sulfotransferase 13

Gene encoding a sulfotransferase involved in proteoglycan modification and potential roles in cancer and development.

Gene Information Card

Symbol CHST13
Full Name Carbohydrate Sulfotransferase 13
Gene Type Protein coding
Chromosomal Location 3q13.33
NCBI Gene ID 150166 ncbi.nlm.nih.gov/gene/150166
Ensembl ID ENSG00000163827
UniProt ID Q8NET6
OMIM ID 610124
HGNC ID 15957
Aliases C4ST3, chondroitin 4-sulfotransferase 3

Description

CHST13 encodes a member of the carbohydrate sulfotransferase family. The enzyme catalyzes the transfer of sulfate to position 4 of N-acetylgalactosamine residues in chondroitin, contributing to the biosynthesis of chondroitin sulfate proteoglycans. These proteoglycans are critical components of the extracellular matrix and are involved in cell signaling, adhesion, and migration. CHST13 expression is implicated in cancer progression and developmental processes.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Colorectal Cancer Altered CHST13 expression may affect tumor cell adhesion and invasion via modification of chondroitin sulfate chains. PubMed: 25691885
Breast Cancer Upregulation of CHST13 is associated with poor prognosis and may promote metastasis through proteoglycan remodeling. PubMed: 29187736
Osteoarthritis Potential role in cartilage matrix degradation due to altered sulfation patterns of chondroitin sulfate. PubMed: 20628086

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 5.2 Low
Colon 12.8 Medium
Breast 8.4 Low
Liver 3.1 Low
Lung 6.7 Low
Kidney 4.5 Low
Cell Line Expression
Cell Line nTPM Notes
HeLa 9.3 Cervical cancer cell line
MCF7 11.5 Breast cancer cell line
HCT116 14.2 Colorectal cancer cell line
A549 7.8 Lung cancer cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.374C>T (p.Thr125Met) Missense <0.01% Unknown functional impact
c.523G>A (p.Gly175Ser) Missense <0.01% Predicted benign by in silico tools
c.788A>G (p.Asn263Ser) Missense <0.01% No known disease association
Mutation functional classification

Loss of Function (LOF)

No confirmed loss-of-function mutations reported in CHST13.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported in CHST13.

Dominant Negative (DN)

No evidence of dominant-negative effects for CHST13 mutations.

Gene Ontology (GO)

N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase activity (GO:0001517) • N-acetylglucosamine metabolic process (GO:0006044)
sulfur compound metabolic process (GO:0006790) • heparan sulfate proteoglycan biosynthetic process (GO:0015014)
• chondroitin sulfate proteoglycan biosynthetic process (GO:0015015) glycosaminoglycan metabolic process (GO:0030203)

Pathways

Chondroitin sulfate/dermatan sulfate biosynthesis (Reactome: R-HSA-1971475)
Glycosaminoglycan metabolism (KEGG: hsa00532)

Protein Summary

CHST13 encodes a 395-amino acid type II transmembrane protein localized to the Golgi apparatus. It functions as a sulfotransferase that transfers sulfate from 3'-phosphoadenosine-5'-phosphosulfate (PAPS) to position 4 of N-acetylgalactosamine residues in chondroitin. This modification is essential for the proper assembly and function of chondroitin sulfate proteoglycans, which modulate cell signaling, extracellular matrix organization, and cell adhesion. The protein is expressed in various tissues, with highest levels in colon and breast. Altered expression is observed in several cancers, suggesting a role in tumor progression.

Related Products

Product name Cat.No. Species Gene ID
CHST13 Knockout HEK293 Cell Line EDJ-KQ12921 Human 166012 Details Get a Quote
CHST13 Knockout HeLa Cell Line EDJ-KQ42128 Human 166012 Details Get a Quote
CHST13 Knockout A-549 Cell Line EDJ-KQ67384 Human 166012 Details Get a Quote
CHST13 Knockout HCT 116 Cell Line EDJ-KQ75776 Human 166012 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
Contact Us
*
*
*
*
How did you hear about us: