Carbohydrate sulfotransferase 6

Summary
UniProt ID
Q9GZX3
Gene Symbol
CHST6
Gene ID
4166
Organism
Homo sapiens (human)
GlyGen
Q9GZX3
The Human Metabolome Database
HMDBP02328
RaftProt
Q9GZX3
Re-Glyco
Q9GZX3
Annotation
Keyword
Carbohydrate metabolism Corneal dystrophy Disease variant Glycoprotein Golgi apparatus Proteomics identification Reference proteome Signal-anchor Transferase Transmembrane helix
Gene Ontology (GO)
GO Hierarchy
Sequence
MWLPRVSSTAVTALLLAQTFLLLFLVSRPGPSSPAGGEARVHVLVLSSWRSGSSFVGQLFNQHPDVFYLMEPAWHVWTTLSQGSAATLHMAVRDLVRSVFLCDMDVFDAYLPWRRNLSDLFQWAVSRALCSPPACSAFPRGAISSEAVCKPLCARQSFTLAREACRSYSHVVLKEVRFFNLQVLYPLLSDPALNLRIVHLVRDPRAVLRSREQTAKALARDNGIVLGTNGTWVEADPGLRVVREVCRSHVRIAEAATLKPPPFLRGRYRLVRFEDLAREPLAEIRALYAFTGLSLTPQLEAWIHNITHGSGPGARREAFKTSSRNALNVSQAWRHALPFAKIRRVQELCAGALQLLGYRPVYSEDEQRNLALDLVLPRGLNGFTWASSTASHPRN
Glycosylation Sites
Displaying all 4 entries
Position Description PubMed ID GlyTouCan ID Source
116
  • N-linked (GlcNAc...) asparagine
229
  • N-linked (GlcNAc...) asparagine
305
  • N-linked (GlcNAc...) asparagine
328
  • N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 2 entries
Pathway Name Organism
Defective CHST6 causes MCDC1 Homo sapiens
Keratan sulfate biosynthesis Homo sapiens
Disease
Displaying 1 entry
DO ID Disease Name Source
DOID:2565 macular corneal dystrophy

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026