GlycoGene Database (GGDB)

GGDB is a database which includes genes associated with glycan synthesis such as glycosyltransferase, sugar nucleotide synthases, sugar-nucleotide transporters, and sulfotransferases.

Database Last Updated
GlycoGene Database (GGDB) January 26, 2018
GGDB ID GGDB Symbol Families Pathway Class Labels Designations Organism
B4GAT1
  • N-Acetylglucosaminyltransferase
  • Glycosaminoglycan, keratan sulfate
  • glycolipid, lacto/neolacto series
  • UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 1
Homo sapiens
CGT
  • Galactosyltransferase
  • sphingolipid
  • UDP-Galactose ceramide galactosyl transferase
Homo sapiens
CHST3
  • Sulfotransferases
  • Glycosaminoglycan, chondroitin sulfate
  • chondroitin 6-sulfotransferase
Homo sapiens
SLC35A3
  • Nucleotide Sugar Transporter
  • SLC/transporter
  • UDP-N-acetylglucosamine transporter
Homo sapiens
HS2ST1
  • Sulfotransferases
  • Glycosaminoglycan, heparan sulfate
  • heparan sulfate 2-O-sulfotransferase
Homo sapiens
SLC35A2
  • Nucleotide Sugar Transporter
  • SLC/transporter
  • UDP-galactose transporter
Homo sapiens
CSGALNACT1
  • N-Acetylgalactosaminyltransferase
  • Glycosaminoglycan, chondroitin sulfate
  • chondroitin sulfate N-acetylgalactosaminyltransferase 1, glucuronosyl-N-acetylgalactosaminyl-proteoglycan 4-beta-N-acetylgalactosaminyltransferase
Homo sapiens
NDST1
  • Sulfotransferases
  • Glycosaminoglycan, heparan sulfate
  • N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
Homo sapiens
GALNT4
  • UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase
  • O-glycan, mucin-type
  • UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase 4
Homo sapiens
LARGE
  • Glucuronyltransferase
  • Xylosyltransferase
  • O-glycan, not mucin-type
  • acetylglucosaminyltransferase-like protein
Homo sapiens
Displaying entries 1 - 10 of 222 in total

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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