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
  • CESD
  • LAL
  • Wolman disease
  • Acid lipase deficiency
  • Lysosomal acid lipase deficiency
Homo sapiens
  • C1GALT2
  • COSMC
gg076
  • Tn polyagglutination syndrome, somatic (SOMATIC MUTATION)
  • Galactosyltransferase Deficiency
  • Tn syndrome (SOMATIC MUTATION)
Homo sapiens
  • CSS1
  • KIAA0990
gg163
  • Temtamy preaxial brachydactyly syndrome
  • TPBS
Homo sapiens
  • Tay-Sachs disease, late-onset forms
  • Juvenile/Chronic/Adult-onset
Homo sapiens
  • MGC13453
  • MRT7
  • MagT2
  • N33
  • OST3A
  • SLC58A2
  • TUSC3-CDG
  • Mental retardation, autosomal recessive 22
  • Mental retardation, autosomal recessive 7 (MRT7)
  • Oligosaccharyltransferase TUSC3 subunit defect
Homo sapiens
  • GDT1
  • SLC64A1
  • TMPT27
  • TPARL
  • TMEM165-CDG
  • CDG-IIk
  • Congenital Disorder of Glycosylation, Type IIk
Homo sapiens
  • C6ST
  • C6ST1
gg025
  • Spondyloepiphyseal dysplasia with congenital joint dislocations
  • Spondyloepiphyseal dysplasia, Omani type
Homo sapiens
  • ATPSK2
  • Spondyloepimetaphyseal dysplasia, pakistani type
  • Brachyolmia 4 with mild epiphyseal and metaphyseal changes
  • SEMD, pakistani type
Homo sapiens
  • Sialidosis type I
  • Cherry-red spot myoclonus syndrome
  • Normosomatic sialidosis
Homo sapiens
  • D22S674
  • Schindler disease, type I
  • infantile type
Homo sapiens
Displaying entries 1 - 10 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