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
RXYLT1		RXYLT1	103820429			Serinus canaria	9135
b3gnt7		b3gnt7	103184417			Callorhinchus milii	7868
DGKQ		DGKQ	101649242			Echinops telfairi	9371
B4GALNT3		B4GALNT3	105529907			Mandrillus leucophaeus	9568
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
ATP6V0A2	ATP6N1D ATP6a2 J6B7 RTF Stv1 TJ6 TJ6M TJ6s V-ATPase subunit a2 V-type proton ATPase 116 kDa subunit a2 Vph1 a2 a2V infantile malignant osteopetrosis regeneration and tolerance factor	ATP6N1D ATP6a2 J6B7 RTF Stv1 TJ6 TJ6M TJ6s V-ATPase subunit a2 V-type proton ATPase 116 kDa subunit a2 Vph1 a2 a2V infantile malignant osteopetrosis regeneration and tolerance factor ATP6V0A2	23545	ATP6VOA2-CDG	ATP6VOA2 defect (cutis laxa type II) Cutis laxa, autosomal recessive, type IIA (ARCL2A) Debre-Type cutis laxa V-ATPase a2 subunit defect	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
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
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
CHST14	D4ST-1 HD4ST	D4ST-1 HD4ST CHST14	113189	Ehlers-Danlos syndrome, musculocontractural type	Adducted thumb and clubfoot syndrome	Homo sapiens	9606