CHST11: Carbohydrate Sulfotransferase 11

Key enzyme in chondroitin sulfate biosynthesis and its role in development and disease

Gene Information Card

Symbol CHST11
Full Name Carbohydrate Sulfotransferase 11
Gene Type Protein coding
Chromosomal Location 12q23.3
NCBI Gene ID 50515 ncbi.nlm.nih.gov/gene/50515
Ensembl ID ENSG00000171310
UniProt ID Q9NPF2
OMIM ID 610191
HGNC ID 19223
Aliases C4ST1, C4ST-1, HSA269257

Description

CHST11 encodes a member of the sulfotransferase family that catalyzes the transfer of sulfate to position 4 of N-acetylgalactosamine residues in chondroitin sulfate. This enzyme is critical for the biosynthesis of chondroitin sulfate, a major component of the extracellular matrix involved in cell signaling, development, and tissue homeostasis. CHST11 is expressed in various tissues and is implicated in skeletal development, cancer progression, and inflammatory responses.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Breast cancer Altered chondroitin sulfate sulfation patterns may promote tumor growth and metastasis COSMIC; PMID: 23542377
Osteoarthritis Dysregulation of chondroitin sulfate sulfation in cartilage contributes to joint degeneration NCBI Gene; PMID: 20037587
Skeletal dysplasia Mutations in CHST11 disrupt chondroitin sulfate biosynthesis, affecting bone development OMIM #610191; PMID: 20037587

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 12.5 Medium
Heart 8.3 Low
Liver 4.1 Low
Lung 15.2 Medium
Kidney 9.7 Low
Skeletal muscle 6.8 Low
Placenta 18.9 Medium
Testis 22.1 High
Cell Line Expression
Cell Line nTPM Notes
HeLa 14.5 Cervical cancer cell line
A549 11.2 Lung cancer cell line
MCF7 9.8 Breast cancer cell line
HEK293 16.3 Embryonic kidney cell line
K562 7.4 Leukemia cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.100C>T (p.Arg34Trp) Missense <0.01% Reduced enzyme activity; associated with skeletal dysplasia
c.487G>A (p.Gly163Arg) Missense <0.01% Loss of function; reported in OMIM
c.763_764insA Frameshift <0.01% Truncated protein; likely loss of function
Mutation functional classification

Loss of Function (LOF)

Missense and frameshift mutations reduce or abolish sulfotransferase activity, impairing chondroitin sulfate biosynthesis.

Gain of Function (GOF)

No gain-of-function mutations reported in CHST11.

Dominant Negative (DN)

No dominant-negative mutations reported in CHST11.

Pathways

Chondroitin sulfate/dermatan sulfate biosynthesis (Reactome: R-HSA-1793185)
Glycosaminoglycan metabolism (KEGG: hsa00532)
Sulfation of glycosaminoglycans (Reactome: R-HSA-1638091)

Protein Summary

CHST11 (C4ST1) is a 411-amino acid type II transmembrane protein localized to the Golgi apparatus. It catalyzes the transfer of sulfate from 3'-phosphoadenosine 5'-phosphosulfate (PAPS) to position 4 of N-acetylgalactosamine residues in chondroitin sulfate. This sulfation step is essential for the formation of chondroitin sulfate chains, which modulate cell adhesion, migration, and signaling. The protein contains a sulfotransferase domain and is expressed in multiple tissues, with highest levels in testis and placenta.

Related Products

Product name Cat.No. Species Gene ID
CHST11 Knockout HEK293 Cell Line EDJ-KQ10766 Human 50515 Details Get a Quote
CHST11 Knockout A-549 Cell Line EDJ-KQ38375 Human 50515 Details Get a Quote
CHST11 Knockout HCT 116 Cell Line EDJ-KQ38376 Human 50515 Details Get a Quote
CHST11 Knockout HeLa Cell Line EDJ-KQ38377 Human 50515 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
Contact Us
*
*
*
*
How did you hear about us: