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 August 23, 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
  • CDGIf
  • Lec35
  • PQLC5
  • SL15
  • SLC66A5
  • MPDU1-CDG
  • CDG-If
  • Congenital disorder of glycosylation, type If
Homo sapiens
MPI
  • MPI-CDG
  • CDG-Ib
  • Congenital disorder of glycosylation, type Ib
  • Mannosephosphate isomerase deficiency
  • Protein-losing enteropathy-hepatic fibrosis syndrome
  • Saguenay-Lac Saint-Jean syndrome
Homo sapiens
gg030
  • Macular corneal dystrophy
  • Macular corneal dystrophy Type I
  • Macular corneal dystrophy Type II
Homo sapiens
  • ASB
411
  • Maroteaux-Lamy syndrome, severe form
Homo sapiens
gg050
  • Mental retardation, autosomal recessive 12
  • MRT12
Homo sapiens
  • ERMan1
  • ERManI
  • MANA-ER
  • MRT15
  • Mental retardation, autosomal recessive 15
  • MRT15
Homo sapiens
  • ASA
410
  • Metachromatic leukodystrophy
Homo sapiens
  • GALNAC6S
  • GAS
  • GalN6S
  • Morquio syndrome A
  • Galactosamine-6-sulphatase deficiency
  • MPS IVA
  • Morquio's syndrome, classic form
  • Mucopolysaccharidosis type IVA
Homo sapiens
  • KIAA1208
  • MGC4170
  • Mucolipidosis II (alpha/beta)
  • I-cell disease
  • ML-II
  • N-Acetylglucosamine-1-phosphotransferase deficiency
Homo sapiens
IDS
  • ID2S
  • Mucopolysaccharidosis II
  • Hunter syndrome
  • MPS II
Homo sapiens
Displaying entries 51 - 60 of 70006 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