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
PSAP		5660	hsa:5660		LMP002838	Gaucher disease, atypical, due to saposin C deficiency	Homo sapiens
GBA1		2629	hsa:2629		LMP000283	Gaucher disease, type II	Homo sapiens
GNE	Uae1	10020	hsa:10020			Hereditary inclusion body myopathy type 2 GNE-CDG (hereditary inclusion body myopathy) Hereditary inclusion body myopathy type 2 (HIBM2) Inclusion body myopathy 2, autosomal recessive (IBM2)	Homo sapiens
PIGV	FLJ20477	55650	hsa:55650	gg223	LMP004710	Hyperphosphatasia with mental retardation syndrome 1 HPMRS1	Homo sapiens
GALC		2581	hsa:2581		LMP002432	Krabbe disease, infantile form	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
LFNG	SCDO3	3955	hsa:3955	gg133		LFNG-CDG SCDO3 Spondylocostal dysostosis 3, autosomal recessive	Homo sapiens
PLOD3	LH3	8985	hsa:8985			Lysyl hydroxylase 3 deficiency Bone fragility with contractures, arterial rupture, and deafness LH3 deficiency	Homo sapiens
MGAT2	GNT-II	4247	hsa:4247	gg126		MGAT2-CDG CDG-IIa Congenital disorder of glycosylation, type IIa	Homo sapiens
MPDU1	CDGIf Lec35 PQLC5 SL15 SLC66A5	9526	hsa:9526			MPDU1-CDG CDG-If Congenital disorder of glycosylation, type If	Homo sapiens