GlyCosmos Glycogenes

Integrated list of glycan-related genes, including glycosyltransferases, hydrolases, etc.

Database Last Updated
FlyGlycoDB September 1, 2018
Glyco-Disease Genes Database (GDGDB) January 25, 2017
GlycoGene Database (GGDB) January 26, 2018
KEGG BRITE July 19, 2022
LIPID MAPSGene/Proteome Database June 24, 2019
Plant GARDEN May 28, 2020
UniProt July 12, 2022
Gene Symbol Alias Symbols Gene ID KEGG GGDB FlyGlycoDB LIPID MAPS Disease Name Species
  • GDT1
  • SLC64A1
  • TMPT27
  • TPARL
  • TMEM165-CDG
  • CDG-IIk
  • Congenital Disorder of Glycosylation, Type IIk
Homo sapiens
  • COD2
  • KIAA1134
  • COG6-CDG
  • CDG-IIL
  • Congenital Disorder of Glycosylation, Type IIL
Homo sapiens
  • KIAA1208
  • MGC4170
  • Mucolipidosis II (alpha/beta)
  • I-cell disease
  • ML-II
  • N-Acetylglucosamine-1-phosphotransferase deficiency
Homo sapiens
  • FLJ13352
  • SRD5A2L
  • SRD5A2L1
  • SRD5A3-CDG
  • CDG-Iq
  • Congenital Disorder of Glycosylation, Type Iq
  • Ocular colobomas, ichthyosis, brain malformations and endocrine abnormalities
Homo sapiens
  • DOR1
  • FLJ22315
  • COG8-CDG
  • CDG-IIh
  • COG8 deficiency
  • Congenital disorder of glycosylation, type IIh
Homo sapiens
  • CDG1N
  • RFT1-CDG
  • CDG-In
  • Congenital disorder of glycosylation, type In
  • RFT1 (flippase) deficiency
Homo sapiens
  • COG7-CDG
  • CDG-IIe
  • Congenital disorder of glycosylation, type IIe
Homo sapiens
  • FLJ32731
  • HGNAT
  • Sanfilippo syndrome C
  • MPS IIIC
  • Mucopolysaccharidosis type IIIC
Homo sapiens
  • FGE
  • UNQ3037
  • Multiple sulfatase deficiency
  • MSD
  • Multiple sulfatase deficiency disease
Homo sapiens
Displaying entries 47691 - 47699 of 47699 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