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
  • GPI-MT-I
  • PIGM-CDG
  • Autosomal recessive GPI anchor deficiency
  • Glycosylphosphatidylinositol deficiency
  • CDG1a
  • CDGS
  • PMI
  • PMI1
  • PMM2-CDG, adult stable disability stage
  • FLJ20277
  • LGMD2O
  • MGAT1.2
  • POMGNT1-CDG (cong. muscular dystrophy spectrum)
  • Muscle-eye-brain disease (MEB)
  • Muscular dystrophy-dystroglycanopathy (Congenital with brain and eye anomalies), type A, 3 (MDDGA3)
  • GPI3
  • PIG-A
  • Paroxysmal nocturnal hemoglobinuria, somatic (SOMATIC MUTATION)
  • PNH1
  • Paroxysmal nocturnal hemoglobinuria 1
GAA
  • Pompe disease
  • GSD type II
  • Lysosomal alpha 1,4 Glucosidase Deficiency Disease
  • CDG1N
  • RFT1-CDG
  • CDG-In
  • Congenital disorder of glycosylation, type In
  • RFT1 (flippase) deficiency
  • CDA-II
  • CDAII
  • HEMPAS
  • SEC23B-CDG
  • CDA II
  • Congenital dyserythropoietic anaemia, type II
  • Hereditary Erythroblastic Multinuclearity with Positive Acidified-Serum Test (HEMPAS)
  • CMPST
  • hCST
  • SLC35A1-CDG
  • CDG-IIf
  • Congenital disorder of glycosylation, type IIf
  • FLJ11320
  • FUCT1
  • SLC35C1-CDG
  • CDG-IIc
  • Congenital disorder of glycosylation, type IIc
  • Leukocyte adhesion deficiency, type 2
  • Rambam Hasharon syndrome
  • KIAA0260
  • UGTREL7
  • SLC35D1-CDG
  • Chondrodysplasia, lethal neonatal, with snail-like pelvis
  • Schneckenbecken dysplasia
Displaying entries 71 - 80 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