GlyCosmos Glycoproteins

Integrated list of glycoproteins extracted from UniProt and annotated with glycosylation data from GlyGen and GlyConnect. For each entry, information such as glycosylation site, glycans, diseases, 3D structures, and pathway information are available.

Database Last Updated
GlyConnect February 2, 2022
GlycoProtDB October 1, 2021
GlyGen February 2, 2022
Human Protein Atlas September 5, 2019 (Protein Atlas version 19)
MCAW-DB July 10, 2019
Reactome February 8, 2021 (Version 79)
UniProt July 20, 2022
Protein Name UniProt ID Gene Symbol Species No. of Glycosylation Sites No. of GlyTouCan IDs Disease Name ▲ Disease Aliases
ALG11
Homo sapiens
2
0
ALG11-CDG
  • CDG-Ip
  • Congenital Disorder of Glycosylation, Type Ip
ALG9
Homo sapiens
2
0
ALG9-CDG
  • CDG-IL
  • Congenital disorder of glycosylation, type IL
ATP6V0A2
Homo sapiens
2
2
ATP6VOA2-CDG
  • ATP6VOA2 defect (cutis laxa type II)
  • Cutis laxa, autosomal recessive, type IIA (ARCL2A)
  • Debre-Type cutis laxa
  • V-ATPase a2 subunit defect
MAN2B1
Homo sapiens
11
16
Alpha-mannosidosis, type I (early-onset)
AGA
Homo sapiens
2
3
Aspartylglucosaminuria
SLC26A2
Homo sapiens
3
0
Autosomal recessive multiple epiphyseal dysplasia
  • Epiphyseal dysplasia, multiple, 4 (EDM4)
B3GLCT
Homo sapiens
1
0
B3GALTL-CDG
  • Krause-Kivlin syndrome
  • Peters anomaly with short limb dwarfism
  • Peters-plus syndrome
B4GALT1
Homo sapiens
1
1
B4GALT1-CDG
  • CDG-IId
  • Congenital disorder of glycosylation, type IId
B4GALT7
Homo sapiens
1
0
B4GALT7-CDG
  • Ehlers-Danlos syndrome, progeroid form
  • Ehlers-Danlos syndrome, progeroid type, 1
  • Galactosyltransferase 1 deficiency
MANBA
Homo sapiens
8
2
Beta-mannosidosis
  • Beta-mannosidase deficiency
Displaying entries 1 - 10 of 65960 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