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
LIPA	CESD LAL Wolman disease lysosomal acid lipase sterol esterase	CESD LAL Wolman disease lysosomal acid lipase sterol esterase LIPA	3988	Wolman disease	Acid lipase deficiency Lysosomal acid lipase deficiency	Homo sapiens	9606
C1GALT1C1	C1GALT2 COSMC	C1GALT2 COSMC C1GALT1C1	29071	Tn polyagglutination syndrome, somatic (SOMATIC MUTATION)	Galactosyltransferase Deficiency Tn syndrome (SOMATIC MUTATION)	Homo sapiens	9606
CHSY1	CSS1 KIAA0990	CSS1 KIAA0990 CHSY1	22856	Temtamy preaxial brachydactyly syndrome	TPBS	Homo sapiens	9606
HEXA	GM2 gangliosidosis Tay Sachs disease beta-hexosaminidase subunit alpha	GM2 gangliosidosis Tay Sachs disease beta-hexosaminidase subunit alpha HEXA	3073	Tay-Sachs disease Tay-Sachs disease, infantile form Tay-Sachs disease, late-onset forms	Acute infantile GM2-Gangliosidosis, B variant GM2-gangliosidosis, type I Hexosaminidase A deficiency Juvenile/Chronic/Adult-onset	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
TMEM165	GDT1 SLC64A1 TMPT27 TPA regulated locus TPARL	GDT1 SLC64A1 TMPT27 TPA regulated locus TPARL TMEM165	55858	TMEM165-CDG	CDG-IIk Congenital Disorder of Glycosylation, Type IIk	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
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
NEU1	sialidase-1	sialidase-1 NEU1	4758	Sialidosis Sialidosis type I Sialidosis type II Sialidosis type II, congenital form Sialidosis type II, infantile form Sialidosis type II, juvenile form	Cherry-red spot myoclonus syndrome Dysmorphic sialidosis Mucolipidosis I Neuraminidase 1 deficiency Neuraminidase deficiency Normosomatic sialidosis	Homo sapiens	9606
NAGA	D22S674 alpha-galactosidase B	D22S674 alpha-galactosidase B NAGA	4668	Schindler disease, type I Schindler disease, type II	Kanzaki disease infantile type	Homo sapiens	9606