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
PAPSS2	ATPSK2	9060	hsa:9060			Spondyloepimetaphyseal dysplasia, pakistani type Brachyolmia 4 with mild epiphyseal and metaphyseal changes SEMD, pakistani type	Homo sapiens
CHST3	C6ST C6ST1	9469	hsa:9469	gg025		Spondyloepiphyseal dysplasia with congenital joint dislocations Spondyloepiphyseal dysplasia, Omani type	Homo sapiens
TMEM165	GDT1 SLC64A1 TMPT27 TPARL	55858	hsa:55858			TMEM165-CDG CDG-IIk Congenital Disorder of Glycosylation, Type IIk	Homo sapiens
TUSC3	MGC13453 MRT7 MagT2 N33 OST3A SLC58A2	7991	hsa:7991			TUSC3-CDG Mental retardation, autosomal recessive 22 Mental retardation, autosomal recessive 7 (MRT7) Oligosaccharyltransferase TUSC3 subunit defect	Homo sapiens
HEXA		3073	hsa:3073		LMP002265	Tay-Sachs disease, late-onset forms Juvenile/Chronic/Adult-onset	Homo sapiens
CHSY1	CSS1 KIAA0990	22856	hsa:22856	gg163		Temtamy preaxial brachydactyly syndrome TPBS	Homo sapiens
C1GALT1C1	C1GALT2 COSMC	29071	hsa:29071	gg076		Tn polyagglutination syndrome, somatic (SOMATIC MUTATION) Galactosyltransferase Deficiency Tn syndrome (SOMATIC MUTATION)	Homo sapiens
LIPA	CESD LAL	3988	hsa:3988		LMP000369	Wolman disease Acid lipase deficiency Lysosomal acid lipase deficiency	Homo sapiens
ABO	A3GALNT A3GALT1	28	hsa:28	gg200	LMP006775		Homo sapiens
EXT1	ttv	2131	hsa:2131	gg158			Homo sapiens