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 July 19, 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
  • CDG1K
  • HMAT1
  • HMT-1
  • Mat-1
gg142
  • ALG1-CDG
  • CDG-Ik
  • Congenital disorder of glycosylation, type Ik
Homo sapiens
  • CDG1P
  • KIAA0266
gg201
  • ALG11-CDG
  • CDG-Ip
  • Congenital Disorder of Glycosylation, Type Ip
Homo sapiens
  • CDG1G
  • ECM39
gg151
  • ALG12-CDG
  • CDG-Ig
  • Congenital disorder of glycosylation, type Ig
Homo sapiens
  • CDG1S
  • FLJ23018
  • MDS031
  • TDRD13
  • YGL047W
gg205
  • ALG13-CDG
  • CDG-Is
  • Congenital Disorder of Glycosylation, Type Is
Homo sapiens
  • CDG1I
  • CDGIi
  • FLJ14511
  • NET38
  • hALPG2
gg143
  • ALG2-CDG
  • CDG-Ii
  • Congenital disorder of glycosylation, type Ii
Homo sapiens
  • CDGS4
  • D16Ertd36e
  • NOT56L
  • Not56
gg144
  • ALG3-CDG
  • CDG-Id
  • Congenital disorder of glycosylation, type Id
Homo sapiens
gg146
  • ALG6-CDG
  • CDG-Ic
  • Congenital disorder of glycosylation, type Ic
Homo sapiens
  • MGC2840
gg147
  • ALG8-CDG
  • CDG-Ih
  • Congenital disorder of glycosylation, type Ih
Homo sapiens
gg148
  • ALG9-CDG
  • CDG-IL
  • Congenital disorder of glycosylation, type IL
Homo sapiens
  • ATP6N1D
  • ATP6a2
  • J6B7
  • RTF
  • Stv1
  • TJ6
  • TJ6M
  • TJ6s
  • Vph1
  • a2
  • a2V
  • ATP6VOA2-CDG
  • ATP6VOA2 defect (cutis laxa type II)
  • Cutis laxa, autosomal recessive, type IIA (ARCL2A)
  • Debre-Type cutis laxa
  • V-ATPase a2 subunit defect
Homo sapiens
Displaying entries 1 - 10 of 47699 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