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
CHST14	D4ST-1 HD4ST	D4ST-1 HD4ST CHST14	113189	Ehlers-Danlos syndrome, musculocontractural type	Adducted thumb and clubfoot syndrome	Homo sapiens	9606
GLA	GALA	GALA GLA	2717	Fabry disease	Alpha-galactosidase A deficiency	Homo sapiens	9606
ASAH1	AC ACDase FLJ21558 PHP32 acid ceramidase acylsphingosine deacylase	AC ACDase FLJ21558 PHP32 acid ceramidase acylsphingosine deacylase ASAH1	427	Farber Lipogranulomatosis Farber Lipogranulomatosis, type 1 Farber Lipogranulomatosis, type 2 Farber Lipogranulomatosis, type 3 Farber Lipogranulomatosis, type 4 Farber Lipogranulomatosis, type 5	Acid Ceramidase Deficiency	Homo sapiens	9606
FUCA1	a-L-fucosidase 1 tissue fucosidase α-L-fucosidase 1	a-L-fucosidase 1 tissue fucosidase α-L-fucosidase 1 FUCA1	2517	Fucosidosis		Homo sapiens	9606
GALNT3	GalNAc-T3 HFTC HHS polypeptide GalNAc transferase 3	GalNAc-T3 HFTC HHS polypeptide GalNAc transferase 3 GALNT3	2591	GALNT3-CDG	Tumoral calcinosis, hyperphosphatemic, familial	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
GLB1	EBP elastin binding protein	EBP elastin binding protein GLB1	2720	GM1-gangliosidosis, type I GM1-gangliosidosis, type II GM1-gangliosidosis, type III Morquio syndrome B	Derry syndrome MPS IVB Morquio-like syndrome Mucopolysaccharidosis type IVB adult form infantile form juvenile form	Homo sapiens	9606
GM2A	GM2-AP GM2-activator protein GM2AP SAP-3 cerebroside sulfate activator protein sphingolipid activator protein 3	GM2-AP GM2-activator protein GM2AP SAP-3 cerebroside sulfate activator protein sphingolipid activator protein 3 GM2A	2760	GM2-gangliosidosis, AB variant	GM2 activator deficiency Tay-Sachs disease, AB variant	Homo sapiens	9606
CTSA	carboxypeptidase C carboxypeptidase Y-like kininase carboxypeptidase-L deamidase lysosomal carboxypeptidase A lysosomal protective protein urinary kininase	carboxypeptidase C carboxypeptidase Y-like kininase carboxypeptidase-L deamidase lysosomal carboxypeptidase A lysosomal protective protein urinary kininase CTSA	5476	Galactosialidosis	Combined deficiency of sialidase AND beta galactosidase	Homo sapiens	9606
GBA1	glucocerebrosidase	glucocerebrosidase GBA1	2629	Gaucher disease, type I Gaucher disease, type II Gaucher disease, type II, neuronopathic form, classic type Gaucher disease, type II, perinatal lethal form Gaucher disease, type III Gaucher disease, type IIIC	neuronopathic form neuronopathic form, cardiovascular form non-neuronopathic form	Homo sapiens	9606