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
SLC26A2	DTDST diastrophic dysplasia sulfate transporter	DTDST diastrophic dysplasia sulfate transporter SLC26A2	1836	Achondrogenesis type IB Autosomal recessive multiple epiphyseal dysplasia Diastrophic dysplasia Neonatal osseous dysplasia I	ACG1B Achondrogenesis, Fraccaro type Atelosteogenesis, type II (AOII) Diastrophic dwarfism Epiphyseal dysplasia, multiple, 4 (EDM4)	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
AGA	ASRG N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase glycosylasparaginase	ASRG N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase glycosylasparaginase AGA	175	Aspartylglucosaminuria		Homo sapiens	9606
B3GLCT	B3GTL B3Glc-T beta-1,3-glucosyltransferase	B3GTL B3Glc-T beta-1,3-glucosyltransferase B3GLCT	145173	B3GALTL-CDG	Krause-Kivlin syndrome Peters anomaly with short limb dwarfism Peters-plus syndrome	Homo sapiens	9606
B4GALT1	Beta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase N-acetyllactosamine synthase beta4Gal-T1 lactose synthase A	Beta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase N-acetyllactosamine synthase beta4Gal-T1 lactose synthase A B4GALT1	2683	B4GALT1-CDG	CDG-IId Congenital disorder of glycosylation, type IId	Homo sapiens	9606
B4GALT7	XGALT-1 beta4Gal-T7 galactosyltransferase I	XGALT-1 beta4Gal-T7 galactosyltransferase I B4GALT7	11285	B4GALT7-CDG	Ehlers-Danlos syndrome, progeroid form Ehlers-Danlos syndrome, progeroid type, 1 Galactosyltransferase 1 deficiency	Homo sapiens	9606
MANBA	beta-mannosidase A	beta-mannosidase A MANBA	4126	Beta-mannosidosis	Beta-mannosidase deficiency	Homo sapiens	9606
COG1	KIAA1381	KIAA1381 COG1	9382	COG1-CDG	CDG-IIg CDGII/COG1 Cerebrocostomandibular-like syndrome COG1 deficiency Congenital disorder of glycosylation, type IIg	Homo sapiens	9606
COG4	COD1 DKFZP586E1519	COD1 DKFZP586E1519 COG4	25839	COG4-CDG	CDG-IIj Congenital disorder of glycosylation, type IIj	Homo sapiens	9606
COG5	GTC90	GTC90 COG5	10466	COG5-CDG	CDG-IIi Congenital disorder of glycosylation, type IIi	Homo sapiens	9606