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 September 1, 2018
Glyco-Disease Genes Database (GDGDB) January 25, 2017
GlycoGene Database (GGDB) January 26, 2018
KEGG BRITE August 28, 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
GNE
  • Uae1
  • bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase
  • Hereditary inclusion body myopathy type 2
  • GNE-CDG (hereditary inclusion body myopathy)
  • Hereditary inclusion body myopathy type 2 (HIBM2)
  • Inclusion body myopathy 2, autosomal recessive (IBM2)
  • FLJ20477
  • GPI mannosyltransferase 2
  • GPI-MT-II
  • PIG-V
  • dol-P-Man dependent GPI mannosyltransferase II
  • Hyperphosphatasia with mental retardation syndrome 1
  • HPMRS1
  • Krabbe disease
  • Krabbe disease
  • Galactosylceramide beta-galactosidase deficiency
  • Globoid cell leukodystrophy
  • Krabbe leukodystrophy
  • Leukodystrophy, globoid cell
  • KIAA0609
  • like-acetylglucosaminyltransferase
  • 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)
  • SCDO3
  • LFNG-CDG
  • SCDO3
  • Spondylocostal dysostosis 3, autosomal recessive
  • LH3
  • Multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3
  • lysyl hydroxlase 3
  • Lysyl hydroxylase 3 deficiency
  • Bone fragility with contractures, arterial rupture, and deafness
  • LH3 deficiency
  • GNT-II
  • MGAT2-CDG
  • CDG-IIa
  • Congenital disorder of glycosylation, type IIa
  • CDGIf
  • Lec35
  • PQLC5
  • SL15
  • SLC66A5
  • MPDU1-CDG
  • CDG-If
  • Congenital disorder of glycosylation, type If
MPI
  • mannose-6-phosphate isomerase
  • MPI-CDG
  • CDG-Ib
  • Congenital disorder of glycosylation, type Ib
  • Mannosephosphate isomerase deficiency
  • Protein-losing enteropathy-hepatic fibrosis syndrome
  • Saguenay-Lac Saint-Jean syndrome
  • Macular corneal dystrophy
  • Macular corneal dystrophy Type I
  • Macular corneal dystrophy Type II
Displaying entries 41 - 50 of 74266 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