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

Gene Symbol	Alias Symbols	Gene ID	KEGG	GGDB	LIPID MAPS	Disease Name ▼	Species
LFNG	SCDO3	3955	hsa:3955	gg133		LFNG-CDG SCDO3 Spondylocostal dysostosis 3, autosomal recessive	Homo sapiens
LARGE1	KIAA0609	9215	hsa:9215	gg171		LARGE-CDG (cong. muscular dystrophy spectrum) Congenital muscular dystrophy type 1D (CMD1D) Muscular dystrophy, congenital, type 1D (MDC1D) Muscular dystrophy-dystroglycanopathy (Congenital with mental retardation), type B, 6 (MDDGB6)	Homo sapiens
GALC		2581	hsa:2581		LMP002432	Krabbe disease, late-onset form	Homo sapiens
PIGV	FLJ20477	55650	hsa:55650	gg223	LMP004710	Hyperphosphatasia with mental retardation syndrome 1 HPMRS1	Homo sapiens
IDUA	MPS1 MPSI	3425	hsa:3425			Hurler-Scheie syndrome MPS1-HS Mucopolysaccharidosis type IH/S	Homo sapiens
GBA1		2629	hsa:2629		LMP000283	Gaucher disease, type I non-neuronopathic form	Homo sapiens
CTSA		5476	hsa:5476			Galactosialidosis Combined deficiency of sialidase AND beta galactosidase	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
GLB1	EBP	2720	hsa:2720		LMP006644	GM1-gangliosidosis, type III adult form	Homo sapiens
MOGS	CWH41 DER7 GCS1	7841	hsa:7841			GCS1-CDG CDG-IIb Congenital disorder of glycosylation, type IIb MOGS-CDG	Homo sapiens