carbohydrate sulfotransferase 6

Summary
Gene Symbol
  • CHST6
Organism
Homo sapiens (human)
NCBI Gene
4166
GGDB ID
HGNC
6938
mRNA
map
  • 16q22
Protein
OMIM
KEGG Gene ID
hsa:4166
PubChem
4166
Alliance of Genome Resources
Annotation
Keyword
  • Carbohydrate metabolism
  • Corneal dystrophy
  • Disease variant
  • Glycoprotein
  • Golgi apparatus
  • Reference proteome
  • Signal-anchor
  • Transferase
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
Q9GZX3
  • Corneal N-acetylglucosamine-6-O-sulfotransferase
  • Galactose/N-acetylglucosamine/N-acetylglucosamine 6-O-sulfotransferase 4-beta
  • N-acetylglucosamine 6-O-sulfotransferase 5
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
sulfotransferase
Functional Category
  • G: Carbohydrate transport and metabolism
  • M: Cell wall/membrane/envelope biogenesis
  • O: Posttranslational modification, protein turnover, chaperones
GlycoGene Database (GGDB)
GGDB ID
gg030
Gene Symbol
  • CHST6
Orthologous Gene
Displaying all 2 entries
Species Protein mRNA
Rattus norvegicus XP_226482 XM_226482
Mus musculus NP_064334 NM_019950
KEGG BRITE Database
Orthology
K09671
Name
carbohydrate 6-sulfotransferase 6 [EC:2.8.2.-]
References
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:2565 macular corneal dystrophy
The Human Phenotype Ontology
Displaying entries 11 - 15 of 15 in total
HPO ID HPO Term
HP:0007759 Opacification of the corneal stroma
HP:0007856 Punctate opacification of the cornea
HP:0012155 Decreased corneal sensation
HP:0100689 Decreased corneal thickness
HP:0200026 Ocular pain
Displaying all 2 entries
Disease ID Disease Name
OMIM:217800
  • macular corneal dystrophy
ORPHA:98969
  • 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: December 9, 2024