Homo sapiens Gene: CHST11
Summary
InnateDB Gene IDBG-54479.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CHST11
Gene Name carbohydrate (chondroitin 4) sulfotransferase 11
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000171310
Encoded Proteins
carbohydrate (chondroitin 4) sulfotransferase 11
carbohydrate (chondroitin 4) sulfotransferase 11
carbohydrate (chondroitin 4) sulfotransferase 11
carbohydrate (chondroitin 4) sulfotransferase 11
carbohydrate (chondroitin 4) sulfotransferase 11
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene belongs to the sulfotransferase 2 family. It is localized to the golgi membrane, and catalyzes the transfer of sulfate to position 4 of the N-acetylgalactosamine (GalNAc) residue of chondroitin. Chondroitin sulfate constitutes the predominant proteoglycan present in cartilage, and is distributed on the surfaces of many cells and extracellular matrices. A chromosomal translocation involving this gene and IgH, t(12;14)(q23;q32), has been reported in a patient with B-cell chronic lymphocytic leukemia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 12:104455295-104762014
Strand Forward strand
Band q23.3
Transcripts
ENST00000303694 ENSP00000305725
ENST00000550711
ENST00000547956 ENSP00000449093
ENST00000549260 ENSP00000450004
ENST00000546689 ENSP00000448678
ENST00000549016 ENSP00000449095
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 0
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0001537 N-acetylgalactosamine 4-O-sulfotransferase activity
GO:0008146 sulfotransferase activity
GO:0047756 chondroitin 4-sulfotransferase activity
GO:0050659 N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase activity
Biological Process
GO:0002063 chondrocyte development
GO:0005975 carbohydrate metabolic process
GO:0007585 respiratory gaseous exchange
GO:0009791 post-embryonic development
GO:0016051 carbohydrate biosynthetic process
GO:0030203 glycosaminoglycan metabolic process
GO:0030204 chondroitin sulfate metabolic process
GO:0030206 chondroitin sulfate biosynthetic process
GO:0030326 embryonic limb morphogenesis
GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway
GO:0033037 polysaccharide localization
GO:0036342 post-anal tail morphogenesis
GO:0042127 regulation of cell proliferation
GO:0042733 embryonic digit morphogenesis
GO:0043066 negative regulation of apoptotic process
GO:0044281 small molecule metabolic process
GO:0048589 developmental growth
GO:0048703 embryonic viscerocranium morphogenesis
GO:0048704 embryonic skeletal system morphogenesis
GO:0051216 cartilage development
Cellular Component
GO:0000139 Golgi membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Chondroitin sulfate biosynthesis pathway
Mucopolysaccharidoses pathway
Myoclonic epilepsy of Lafora pathway
Defective B4GALT7 causes EDS, progeroid type pathway
Defective CHST6 causes MCDC1 pathway
MPS VI - Maroteaux-Lamy syndrome pathway
Defective PAPSS2 causes SEMD-PA pathway
Metabolism of carbohydrates pathway
MPS IIID - Sanfilippo syndrome D pathway
Defective SLC26A2 causes chondrodysplasias pathway
MPS IX - Natowicz syndrome pathway
Defective EXT1 causes exostoses 1, TRPS2 and CHDS pathway
Defective CHST14 causes EDS, musculocontractural type pathway
MPS IV - Morquio syndrome B pathway
Defective B3GAT3 causes JDSSDHD pathway
Defective CHST3 causes SEDCJD pathway
MPS IV - Morquio syndrome A pathway
Defective EXT2 causes exostoses 2 pathway
Diseases associated with glycosaminoglycan metabolism pathway
MPS II - Hunter syndrome pathway
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) pathway
Glycosaminoglycan metabolism pathway
Diseases of glycosylation pathway
Chondroitin sulfate/dermatan sulfate metabolism pathway
MPS VII - Sly syndrome pathway
Defective CHSY1 causes TPBS pathway
Metabolism pathway
MPS I - Hurler syndrome pathway
MPS IIIA - Sanfilippo syndrome A pathway
MPS IIIC - Sanfilippo syndrome C pathway
Disease pathway
Glycogen storage diseases pathway
MPS IIIB - Sanfilippo syndrome B pathway
KEGG
Glycosaminoglycan biosynthesis pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.17569 Hs.717994
RefSeq NM_001173982 NM_018413
HUGO
OMIM
CCDS CCDS55878 CCDS9099
HPRD 13055
IMGT
EMBL
GenPept
RNA Seq Atlas