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
EXTL3
  • N-Acetylglucosaminyltransferase
  • Glycosaminoglycan, heparan sulfate
  • heparan sulfate GlcA/GlcNAc transferase like 3
Homo sapiens
B3GNT8
  • N-Acetylglucosaminyltransferase
  • N-glycan
  • UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8
Homo sapiens
OGT
  • N-Acetylglucosaminyltransferase
  • O-glycan, not mucin-type
  • O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase)
Homo sapiens
PIGC
  • N-Acetylglucosaminyltransferase
  • GPI-anchor
  • GlcNAc-T complex; 2 transcipt variants(NM_153747.1, NM_002642.3)
Homo sapiens
GCNT1
  • N-Acetylglucosaminyltransferase
  • O-glycan, mucin-type
  • glucosaminyl (N-acetyl) transferase 1, core 2 (beta-1,6-N-acetylglucosaminyltransferase)
Homo sapiens
MGAT4B
  • N-Acetylglucosaminyltransferase
  • N-glycan
  • mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme B
Homo sapiens
PIGY
  • N-Acetylglucosaminyltransferase
  • GPI-anchor
  • GlcNAc-T complex
Homo sapiens
MGAT5
  • N-Acetylglucosaminyltransferase
  • N-glycan
  • mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase
Homo sapiens
PIGP
  • N-Acetylglucosaminyltransferase
  • GPI-anchor
  • GlcNAc-T complex; 2 transcript variants (NM_153681.2, NM_153682.2)
Homo sapiens
PIGA
  • N-Acetylglucosaminyltransferase
  • GPI-anchor
  • GlcNAc-T complex; 2 transcript variants (NM_002641.3, NM_020473.3)
Homo sapiens
Displaying entries 111 - 120 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