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 ID	Disease Name ▼	Species
GLA	GALA	2717	Fabry disease	Homo sapiens
CHST14	D4ST-1 HD4ST	113189	Ehlers-Danlos syndrome, musculocontractural type	Homo sapiens
DPM3	DPM synthase complex subunit MGC125904 MGC125905 MGC34275	54344	DPM3-CDG	Homo sapiens
DPM1	CDGIE DPM synthase complex, catalytic subunit MPDS	8813	DPM1-CDG	Homo sapiens
DPAGT1	ALG7 CDG-Ij D11S366 DGPT GPT GlcNAc-1-P transferase 1 UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	1798	DPAGT1-CDG	Homo sapiens
DOLK	DK1 KIAA1094 dolichol kinase 1	22845	DOLK-CDG	Homo sapiens
DDOST	KIAA0115 OST OST48 WBP1 advanced glycation end-product receptor 1 oligosaccharyltransferase subunit 48	1650	DDOST-CDG	Homo sapiens
PSAP	saposin-A saposin-B saposin-C saposin-D variant Gaucher disease and variant metachromatic leukodystrophy	5660	Combined saposin deficiency Gaucher disease, atypical, due to saposin C deficiency Metachromatic leukodystrophy, due to saposin B deficiency	Homo sapiens
FKTN	LGMD2M	2218	Cardiomyopathy, dilated, 1X Fukuyama congenital muscular dystrophy Muscular dystrophy, limb-girdle, type 2M	Homo sapiens
COG8	DOR1 FLJ22315	84342	COG8-CDG	Homo sapiens