GlyCosmos Glycogenes

Integrated list of glycan-related genes, including glycosyltransferases, hydrolases, etc. Gene Symbol Aliases include gene descriptions and names of orthologs.

Database Last Updated
FlyGlycoDB March 25, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
GlycoGene Database (GGDB) January 26, 2018
KEGG BRITE September 20, 2023
LIPID MAPSGene/Proteome Database June 24, 2019
Plant GARDEN May 28, 2020
UniProt August 23, 2023
Human Phenotype Ontology July 12, 2023
Gene Symbol Gene Symbol Aliases Gene ID Disease Name ▼ Species
  • CESD
  • LAL
  • Wolman disease
  • lysosomal acid lipase
  • sterol esterase
  • Wolman disease
  • C1GALT2
  • COSMC
  • Tn polyagglutination syndrome, somatic (SOMATIC MUTATION)
  • CSS1
  • KIAA0990
  • Temtamy preaxial brachydactyly syndrome
  • GM2 gangliosidosis
  • Tay Sachs disease
  • beta-hexosaminidase subunit alpha
  • Tay-Sachs disease
  • Tay-Sachs disease, infantile form
  • Tay-Sachs disease, late-onset forms
  • MGC13453
  • MRT7
  • MagT2
  • Magnesium uptake/transporter TUSC3
  • N33
  • OST3A
  • SLC58A2
  • oligosaccharyltransferase 3 homolog A (S. cerevisiae)
  • TUSC3-CDG
  • GDT1
  • SLC64A1
  • TMPT27
  • TPA regulated locus
  • TPARL
  • TMEM165-CDG
  • C6ST
  • C6ST1
  • chondroitin 6 sulfotransferase 1
  • Spondyloepiphyseal dysplasia with congenital joint dislocations
  • ATPSK2
  • PAPS synthase 2
  • adenosine 5'-phosphosulfate kinase
  • bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 2
  • Spondyloepimetaphyseal dysplasia, pakistani type
  • sialidase-1
  • Sialidosis
  • Sialidosis type I
  • Sialidosis type II
  • Sialidosis type II, congenital form
  • Sialidosis type II, infantile form
  • Sialidosis type II, juvenile form
  • D22S674
  • alpha-galactosidase B
  • Schindler disease, type I
  • Schindler disease, type II
Displaying entries 1 - 10 of 394512 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