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
SUMF1	FGE UNQ3037	FGE UNQ3037 SUMF1	285362	Multiple sulfatase deficiency	MSD Multiple sulfatase deficiency disease	Homo sapiens	9606
B3GAT3	GlcAT-I galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 glucuronosyltransferase I	GlcAT-I galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 glucuronosyltransferase I B3GAT3	26229	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects		Homo sapiens	9606
PIGN	GPI ethanolamine phosphate transferase 1 MCD4 PIG-N	GPI ethanolamine phosphate transferase 1 MCD4 PIG-N PIGN	23556	Multiple congenital anomalies-hypotonia-seizures syndrome 1	MCAHS1	Homo sapiens	9606
GUSB		GUSB	2990	Mucopolysaccharidosis VII	MPS VII Sly syndrome	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
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
ARSA	ASA metachromatic leucodystrophy	ASA metachromatic leucodystrophy ARSA	410	Metachromatic leukodystrophy Metachromatic leukodystrophy, adult form Metachromatic leukodystrophy, infantile form Metachromatic leukodystrophy, juvenile form		Homo sapiens	9606
MAN1B1	ER alpha 1,2-mannosidase ERMan1 ERManI MANA-ER MRT15 Man9GlcNAc2-specific processing alpha-mannosidase alpha 1,2-mannosidase endoplasmic Reticulum Class I alpha-mannosidase endoplasmic reticulum alpha-mannosidase 1 endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase 1	ER alpha 1,2-mannosidase ERMan1 ERManI MANA-ER MRT15 Man9GlcNAc2-specific processing alpha-mannosidase alpha 1,2-mannosidase endoplasmic Reticulum Class I alpha-mannosidase endoplasmic reticulum alpha-mannosidase 1 endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase 1 MAN1B1	11253	Mental retardation, autosomal recessive 15	MRT15	Homo sapiens	9606
ST3GAL3	N-acetyllactosaminide alpha-2,3-sialyltransferase ST3Gal III	N-acetyllactosaminide alpha-2,3-sialyltransferase ST3Gal III ST3GAL3	6487	Mental retardation, autosomal recessive 12	MRT12	Homo sapiens	9606