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
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
SMPD1	ASM Niemann-Pick type A/B acid sphingomyelinase	ASM Niemann-Pick type A/B acid sphingomyelinase SMPD1	6609	Niemann-Pick disease, type A Niemann-Pick disease, type B	neurological type non-neurological type	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
CHSY1	CSS1 KIAA0990	CSS1 KIAA0990 CHSY1	22856	Temtamy preaxial brachydactyly syndrome	TPBS	Homo sapiens	9606
CHST3	C6ST C6ST1 chondroitin 6 sulfotransferase 1	C6ST C6ST1 chondroitin 6 sulfotransferase 1 CHST3	9469	Spondyloepiphyseal dysplasia with congenital joint dislocations	Spondyloepiphyseal dysplasia, Omani type	Homo sapiens	9606
PSAP	saposin-A saposin-B saposin-C saposin-D variant Gaucher disease and variant metachromatic leukodystrophy	saposin-A saposin-B saposin-C saposin-D variant Gaucher disease and variant metachromatic leukodystrophy PSAP	5660	Combined saposin deficiency Gaucher disease, atypical, due to saposin C deficiency Metachromatic leukodystrophy, due to saposin B deficiency	Sphingolipid activator protein 1 deficiency prosaposin deficiency saposin deficiency	Homo sapiens	9606
LFNG	SCDO3	SCDO3 LFNG	3955	LFNG-CDG	SCDO3 Spondylocostal dysostosis 3, autosomal recessive	Homo sapiens	9606
PIGA	GPI3 GPI3 (SPT14) homolog (S. cerevisiae) PIG-A Phosphatidylinositol N-acetylglucosaminyltransferase subunit A paroxysmal nocturnal hemoglobinuria	GPI3 GPI3 (SPT14) homolog (S. cerevisiae) PIG-A Phosphatidylinositol N-acetylglucosaminyltransferase subunit A paroxysmal nocturnal hemoglobinuria PIGA	5277	Paroxysmal nocturnal hemoglobinuria, somatic (SOMATIC MUTATION)	PNH1 Paroxysmal nocturnal hemoglobinuria 1	Homo sapiens	9606
POMGNT1	FLJ20277 LGMD2O MGAT1.2 protein O-mannose beta-1,2-N-acetylglucosaminyltransferase	FLJ20277 LGMD2O MGAT1.2 protein O-mannose beta-1,2-N-acetylglucosaminyltransferase POMGNT1	55624	POMGNT1-CDG (cong. muscular dystrophy spectrum)	Muscle-eye-brain disease (MEB) Muscular dystrophy-dystroglycanopathy (Congenital with brain and eye anomalies), type A, 3 (MDDGA3)	Homo sapiens	9606
TUSC3	MGC13453 MRT7 MagT2 Magnesium uptake/transporter TUSC3 N33 OST3A SLC58A2 oligosaccharyltransferase 3 homolog A (S. cerevisiae)	MGC13453 MRT7 MagT2 Magnesium uptake/transporter TUSC3 N33 OST3A SLC58A2 oligosaccharyltransferase 3 homolog A (S. cerevisiae) TUSC3	7991	TUSC3-CDG	Mental retardation, autosomal recessive 22 Mental retardation, autosomal recessive 7 (MRT7) Oligosaccharyltransferase TUSC3 subunit defect	Homo sapiens	9606