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
  • LAMAN
  • Alpha-mannosidosis, type I (early-onset)
Homo sapiens
AGA
  • ASRG
175
  • Aspartylglucosaminuria
Homo sapiens
  • DTDST
  • Autosomal recessive multiple epiphyseal dysplasia
  • Epiphyseal dysplasia, multiple, 4 (EDM4)
Homo sapiens
  • B3GTL
  • B3Glc-T
gg184
  • B3GALTL-CDG
  • Krause-Kivlin syndrome
  • Peters anomaly with short limb dwarfism
  • Peters-plus syndrome
Homo sapiens
  • beta4Gal-T1
gg077
  • B4GALT1-CDG
  • CDG-IId
  • Congenital disorder of glycosylation, type IId
Homo sapiens
  • XGALT-1
  • beta4Gal-T7
gg083
  • B4GALT7-CDG
  • Ehlers-Danlos syndrome, progeroid form
  • Ehlers-Danlos syndrome, progeroid type, 1
  • Galactosyltransferase 1 deficiency
Homo sapiens
  • Beta-mannosidosis
  • Beta-mannosidase deficiency
Homo sapiens
  • LH2
  • TLH
  • Bruck syndrome 2
  • BRKS2
  • Osteogenesis imperfecta with congenital joint contractures
Homo sapiens
  • KIAA1381
  • COG1-CDG
  • CDG-IIg
  • CDGII/COG1 Cerebrocostomandibular-like syndrome
  • COG1 deficiency
  • Congenital disorder of glycosylation, type IIg
Homo sapiens
  • COD1
  • DKFZP586E1519
  • COG4-CDG
  • CDG-IIj
  • Congenital disorder of glycosylation, type IIj
Homo sapiens
Displaying entries 11 - 20 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