GlyCosmos Portal

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	LIPID MAPS	Disease Name ▲	Species
CHST14	D4ST-1 HD4ST	113189	hsa:113189	gg040		Ehlers-Danlos syndrome, musculocontractural type Adducted thumb and clubfoot syndrome	Homo sapiens
PLOD1	LH1	5351	hsa:5351			Ehlers-Danlos syndrome, type VI Ehlers-Danlos syndrome, kyphoscoliotic type Nevo syndrome	Homo sapiens
GLA	GALA	2717	hsa:2717		LMP000589	Fabry disease Alpha-galactosidase A deficiency	Homo sapiens
ASAH1	AC ACDase FLJ21558 PHP32	427	hsa:427		LMP002014	Farber Lipogranulomatosis, type 2	Homo sapiens
FUCA1		2517	hsa:2517			Fucosidosis	Homo sapiens
GALNT3	GalNAc-T3 HFTC HHS	2591	hsa:2591	gg089		GALNT3-CDG Tumoral calcinosis, hyperphosphatemic, familial	Homo sapiens
MOGS	CWH41 DER7 GCS1	7841	hsa:7841			GCS1-CDG CDG-IIb Congenital disorder of glycosylation, type IIb MOGS-CDG	Homo sapiens
GLB1	EBP	2720	hsa:2720		LMP006644	GM1-gangliosidosis, type II Derry syndrome juvenile form	Homo sapiens
GM2A	GM2-AP GM2AP SAP-3	2760	hsa:2760		LMP000886	GM2-gangliosidosis, AB variant GM2 activator deficiency Tay-Sachs disease, AB variant	Homo sapiens
CTSA		5476	hsa:5476			Galactosialidosis Combined deficiency of sialidase AND beta galactosidase	Homo sapiens