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
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