GlyCosmos Portal

GlyCosmos Glycogenes

Integrated list of glycan-related genes, including glycosyltransferases, hydrolases, etc. Gene Symbol Aliases include gene descriptions and names of orthologs.

Database	Last Updated
FlyGlycoDB	March 25, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017
GlycoGene Database (GGDB)	January 26, 2018
KEGG BRITE	September 20, 2023
LIPID MAPSGene/Proteome Database	June 24, 2019
Plant GARDEN	May 28, 2020
UniProt	August 23, 2023
Human Phenotype Ontology	July 12, 2023

Gene Symbol	Gene Symbol Aliases	Gene Symbol All	Gene ID	Disease Name	Aliases Disease Name ▲	Species	Taxonomy ID
HEXB	beta-hexosaminidase subunit beta	beta-hexosaminidase subunit beta HEXB	3074	Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile form	GM2-gangliosidosis, type II	Homo sapiens	9606
GAA	Pompe disease glycogen storage disease type II	Pompe disease glycogen storage disease type II GAA	2548	Pompe disease Pompe disease, infantile-onset form Pompe disease, late-onset form	GSD type II Lysosomal alpha 1,4 Glucosidase Deficiency Disease	Homo sapiens	9606
GALNS	GALNAC6S GAS GalN6S Morquio syndrome N-acetylgalactosamine-6-sulfatase chondroitinase chondroitinsulfatase galactose-6-sulfate sulfatase mucopolysaccharidosis type IVA	GALNAC6S GAS GalN6S Morquio syndrome N-acetylgalactosamine-6-sulfatase chondroitinase chondroitinsulfatase galactose-6-sulfate sulfatase mucopolysaccharidosis type IVA GALNS	2588	Morquio syndrome A	Galactosamine-6-sulphatase deficiency MPS IVA Morquio's syndrome, classic form Mucopolysaccharidosis type IVA	Homo sapiens	9606
GALC	Krabbe disease	Krabbe disease GALC	2581	Krabbe disease Krabbe disease, infantile form Krabbe disease, late-onset form	Galactosylceramide beta-galactosidase deficiency Globoid cell leukodystrophy Krabbe leukodystrophy Leukodystrophy, globoid cell	Homo sapiens	9606
C1GALT1C1	C1GALT2 COSMC	C1GALT2 COSMC C1GALT1C1	29071	Tn polyagglutination syndrome, somatic (SOMATIC MUTATION)	Galactosyltransferase Deficiency Tn syndrome (SOMATIC MUTATION)	Homo sapiens	9606
IDUA	MPS1 MPSI mucopolysaccharidosis type I	MPS1 MPSI mucopolysaccharidosis type I IDUA	3425	Hurler syndrome Hurler-Scheie syndrome Scheie syndrome	Gargoylism, Hurler syndrome MPS1-H MPS1-HS MPS1-S Mucopolysaccharidosis type IH Mucopolysaccharidosis type IH/S Mucopolysaccharidosis type IS Mucopolysaccharidosis type V Pfaundler-Hurler syndrome Scheie's syndrome	Homo sapiens	9606
PIGV	FLJ20477 GPI mannosyltransferase 2 GPI-MT-II PIG-V dol-P-Man dependent GPI mannosyltransferase II	FLJ20477 GPI mannosyltransferase 2 GPI-MT-II PIG-V dol-P-Man dependent GPI mannosyltransferase II PIGV	55650	Hyperphosphatasia with mental retardation syndrome 1	HPMRS1	Homo sapiens	9606
IDS	Hunter syndrome ID2S	Hunter syndrome ID2S IDS	3423	Mucopolysaccharidosis II	Hunter syndrome MPS II	Homo sapiens	9606
GNPTAB	KIAA1208 MGC4170	KIAA1208 MGC4170 GNPTAB	79158	Mucolipidosis II (alpha/beta) Mucolipidosis III (alpha/beta)	I-cell disease ML-II ML-III N-Acetylglucosamine-1-phosphotransferase deficiency Pseudo-Hurler Polydystrophy	Homo sapiens	9606
NAGA	D22S674 alpha-galactosidase B	D22S674 alpha-galactosidase B NAGA	4668	Schindler disease, type I Schindler disease, type II	Kanzaki disease infantile type	Homo sapiens	9606