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
  • DPM:GlcN-(acyl-)PI mannosyltransferase
  • GPI mannosyltransferase 1
  • GPI-MT-I
  • PIG-M
  • dol-P-Man dependent GPI mannosyltransferase
  • PIGM-CDG
  • Autosomal recessive GPI anchor deficiency
  • Glycosylphosphatidylinositol deficiency
  • CDG1a
  • CDGS
  • Congenital disorder of glycosylation, type Ia
  • PMI
  • PMI1
  • mannose-6-phosphate isomerase
  • phosphomannose isomerase 1
  • PMM2-CDG, late-infantile and childhood ataxia-intellectual disability stage
  • FLJ20277
  • LGMD2O
  • MGAT1.2
  • protein O-mannose beta-1,2-N-acetylglucosaminyltransferase
  • 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
  • GPI3 (SPT14) homolog (S. cerevisiae)
  • PIG-A
  • Phosphatidylinositol N-acetylglucosaminyltransferase subunit A
  • paroxysmal nocturnal hemoglobinuria
  • Paroxysmal nocturnal hemoglobinuria, somatic (SOMATIC MUTATION)
  • PNH1
  • Paroxysmal nocturnal hemoglobinuria 1
GAA
  • Pompe disease
  • glycogen storage disease type II
  • Pompe disease
  • GSD type II
  • Lysosomal alpha 1,4 Glucosidase Deficiency Disease
  • CDG1N
  • congenital disorder of glycosylation 1N
  • 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)
  • CMP-Sia-Tr
  • CMP-sialic acid transporter
  • CMPST
  • hCST
  • SLC35A1-CDG
  • CDG-IIf
  • Congenital disorder of glycosylation, type IIf
  • FLJ11320
  • FUCT1
  • GDP-fucose transporter 1
  • SLC35C1-CDG
  • CDG-IIc
  • Congenital disorder of glycosylation, type IIc
  • Leukocyte adhesion deficiency, type 2
  • Rambam Hasharon syndrome
  • KIAA0260
  • UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter
  • UGTREL7
  • SLC35D1-CDG
  • Chondrodysplasia, lethal neonatal, with snail-like pelvis
  • Schneckenbecken dysplasia
Displaying entries 71 - 80 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