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
B4GALNT2
  • N-Acetylgalactosaminyltransferase
  • N-glycan
  • O-glycan, mucin-type
  • glycolipid, ganglio series
  • beta 1,4 N-acetylgalactosaminyltransferase 2
Homo sapiens
ST8SIA4
  • Sialyltransferase
  • N-glycan
  • O-glycan, mucin-type
  • ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4
Homo sapiens
ST6GAL1
  • Sialyltransferase
  • N-glycan
  • O-glycan, not mucin-type
  • CMP-NeuAc:galactoside alpha-2,6-sialyltransferase
Homo sapiens
ST6GAL2
  • Sialyltransferase
  • N-glycan
  • O-glycan, not mucin-type
  • CMP-NeuAc:galactoside alpha-2,6-sialyltransferase
Homo sapiens
MGAT5B
  • N-Acetylglucosaminyltransferase
  • N-glycan
  • O-glycan, not mucin-type
  • mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B
Homo sapiens
ST8SIA3
  • Sialyltransferase
  • N-glycan
  • glycolipid, ganglio series
  • ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3
Homo sapiens
ALG8
  • Glucosyltransferase
  • N-glycan
  • Dol-P-Glucose:GlcMan9GlcNAc2-PP-dolichol alpha-1,3-glucosyltransferase
Homo sapiens
ALG3
  • Mannosyltransferases
  • N-glycan
  • Dol-P-Mannose:Man5GlcNAc2-PP-dolichol alpha-1,3-mannosyltransferase
Homo sapiens
ALG14
  • N-Acetylglucosaminyltransferase
  • N-glycan
  • asparagine-linked glycosylation 14 homolog (yeast)
Homo sapiens
MGAT1
  • N-Acetylglucosaminyltransferase
  • N-glycan
  • mannosyl (alpha-1,3-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
Homo sapiens
Displaying entries 81 - 90 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