GlyCosmos Portal

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	October 28, 2022 (Version 82)
UniProt	September 8, 2022

Protein Name	UniProt ID	Gene Symbol	Alias Symbols	Species	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Name ▲	Disease Aliases
GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase	Q2TAA5	ALG11	GT8	Homo sapiens	2	0	ALG11-CDG	CDG-Ip Congenital Disorder of Glycosylation, Type Ip
Alpha-1,2-mannosyltransferase ALG9	Q9H6U8	ALG9	DIBD1	Homo sapiens	2	0	ALG9-CDG	CDG-IL Congenital disorder of glycosylation, type IL
V-type proton ATPase 116 kDa subunit a 2	Q9Y487	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
Lysosomal alpha-mannosidase	O00754	MAN2B1	LAMAN MANB	Homo sapiens	11	16	Alpha-mannosidosis	Alpha-mannosidase B deficiency
N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase	P20933	AGA		Homo sapiens	2	3	Aspartylglucosaminuria
Beta-1,3-glucosyltransferase	Q6Y288	B3GLCT	B3GALTL B3GTL	Homo sapiens	1	0	B3GALTL-CDG	Krause-Kivlin syndrome Peters anomaly with short limb dwarfism Peters-plus syndrome
Beta-1,4-galactosyltransferase 1	P15291	B4GALT1	GGTB2	Homo sapiens	1	1	B4GALT1-CDG	CDG-IId Congenital disorder of glycosylation, type IId
Beta-1,4-galactosyltransferase 7	Q9UBV7	B4GALT7	XGALT1	Homo sapiens	1	0	B4GALT7-CDG	Ehlers-Danlos syndrome, progeroid form Ehlers-Danlos syndrome, progeroid type, 1 Galactosyltransferase 1 deficiency
Beta-mannosidase	O00462	MANBA	MANB1	Homo sapiens	8	2	Beta-mannosidosis	Beta-mannosidase deficiency
Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2	O00469	PLOD2		Homo sapiens	7	9	Bruck syndrome 2	BRKS2 Osteogenesis imperfecta with congenital joint contractures