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
GLA	GALA	GALA GLA	2717	Fabry disease	Alpha-galactosidase A deficiency	Homo sapiens	9606
MAN2B1	LAMAN lysosomal alpha-mannosidase	LAMAN lysosomal alpha-mannosidase MAN2B1	4125	Alpha-mannosidosis Alpha-mannosidosis, type I (early-onset) Alpha-mannosidosis, type II (later-onset)	Alpha-mannosidase B deficiency	Homo sapiens	9606
ST3GAL5	SIATGM3S ST3GalV ganglioside GM3 synthase lactosylceramide alpha-2,3-sialyltransferase	SIATGM3S ST3GalV ganglioside GM3 synthase lactosylceramide alpha-2,3-sialyltransferase ST3GAL5	8869	ST3GAL5-CDG	Amish infantile epilepsy syndrome Epilepsy syndrome, infantile-onset symptomatic GM3 Synthase deficiency	Homo sapiens	9606
PIGM	DPM:GlcN-(acyl-)PI mannosyltransferase GPI mannosyltransferase 1 GPI-MT-I PIG-M dol-P-Man dependent GPI mannosyltransferase	DPM:GlcN-(acyl-)PI mannosyltransferase GPI mannosyltransferase 1 GPI-MT-I PIG-M dol-P-Man dependent GPI mannosyltransferase PIGM	93183	PIGM-CDG	Autosomal recessive GPI anchor deficiency Glycosylphosphatidylinositol deficiency	Homo sapiens	9606
MANBA	beta-mannosidase A	beta-mannosidase A MANBA	4126	Beta-mannosidosis	Beta-mannosidase deficiency	Homo sapiens	9606
PLOD3	LH3 Multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3 lysyl hydroxlase 3	LH3 Multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3 lysyl hydroxlase 3 PLOD3	8985	Lysyl hydroxylase 3 deficiency	Bone fragility with contractures, arterial rupture, and deafness LH3 deficiency	Homo sapiens	9606
PAPSS2	ATPSK2 PAPS synthase 2 adenosine 5'-phosphosulfate kinase bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 2	ATPSK2 PAPS synthase 2 adenosine 5'-phosphosulfate kinase bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 2 PAPSS2	9060	Spondyloepimetaphyseal dysplasia, pakistani type	Brachyolmia 4 with mild epiphyseal and metaphyseal changes SEMD, pakistani type	Homo sapiens	9606
COG6	COD2 KIAA1134	COD2 KIAA1134 COG6	57511	COG6-CDG	CDG-IIL Congenital Disorder of Glycosylation, Type IIL	Homo sapiens	9606
MGAT2	GNT-II	GNT-II MGAT2	4247	MGAT2-CDG	CDG-IIa Congenital disorder of glycosylation, type IIa	Homo sapiens	9606
MOGS	CWH41 DER7 GCS1 glucosidase I processing A-glucosidase I	CWH41 DER7 GCS1 glucosidase I processing A-glucosidase I MOGS	7841	GCS1-CDG	CDG-IIb Congenital disorder of glycosylation, type IIb MOGS-CDG	Homo sapiens	9606