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
Human Phenotype Ontology July 12, 2023
Gene Symbol Gene Symbol Aliases ▲ Gene ID KEGG ID GGDB ID FlyGlycoDB LIPID MAPS Disease Name Species
PIGS
94005
gg232
LMP000789
MPI
4351
hsa:4351
  • MPI-CDG
  • CDG-Ib
  • Congenital disorder of glycosylation, type Ib
  • Mannosephosphate isomerase deficiency
  • Protein-losing enteropathy-hepatic fibrosis syndrome
  • Saguenay-Lac Saint-Jean syndrome
PGM1
5236
hsa:5236
  • PGM1-CDG
  • CDG-It
  • Congenital Disorder of Glycosylation, Type It
CTSA
5476
hsa:5476
  • Galactosialidosis
  • Combined deficiency of sialidase AND beta galactosidase
PSAP
5660
hsa:5660
LMP002838
  • Gaucher disease, atypical, due to saposin C deficiency
COG7
91949
hsa:91949
  • COG7-CDG
  • CDG-IIe
  • Congenital disorder of glycosylation, type IIe
Displaying entries 70001 - 70006 of 70006 in total
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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

  • © GlyCosmos Portal v3.3.0
  • Last updated: August 14, 2023