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
  • GM2-AP
  • GM2AP
  • SAP-3
  • GM2-gangliosidosis, AB variant
  • GM2 activator deficiency
  • Tay-Sachs disease, AB variant
Homo sapiens
  • Galactosialidosis
  • Combined deficiency of sialidase AND beta galactosidase
Homo sapiens
  • Gaucher disease, type I
  • non-neuronopathic form
Homo sapiens
  • MPS1
  • MPSI
  • Hurler-Scheie syndrome
  • MPS1-HS
  • Mucopolysaccharidosis type IH/S
Homo sapiens
  • FLJ20477
gg223
  • Hyperphosphatasia with mental retardation syndrome 1
  • HPMRS1
Homo sapiens
  • Krabbe disease, late-onset form
Homo sapiens
  • KIAA0609
gg171
  • LARGE-CDG (cong. muscular dystrophy spectrum)
  • Congenital muscular dystrophy type 1D (CMD1D)
  • Muscular dystrophy, congenital, type 1D (MDC1D)
  • Muscular dystrophy-dystroglycanopathy (Congenital with mental retardation), type B, 6 (MDDGB6)
Homo sapiens
  • SCDO3
gg133
  • LFNG-CDG
  • SCDO3
  • Spondylocostal dysostosis 3, autosomal recessive
Homo sapiens
  • LH3
  • Lysyl hydroxylase 3 deficiency
  • Bone fragility with contractures, arterial rupture, and deafness
  • LH3 deficiency
Homo sapiens
  • GNT-II
gg126
  • MGAT2-CDG
  • CDG-IIa
  • Congenital disorder of glycosylation, type IIa
Homo sapiens
Displaying entries 41 - 50 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