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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	October 29, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Search results for "glycosyltransferase activity"

Displaying entries **26 - 50** of **140930** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
2589	polypeptide N-acetylgalactosaminyltransferase 1	GALNT1 Aliases: GalNAc-T1 polypeptide GalNAc transferase 1 protein-UDP acetylgalactosaminyltransferase 1	Homo sapiens (human)
2590	polypeptide N-acetylgalactosaminyltransferase 2	GALNT2 Aliases: GalNAc-T2 polypeptide GalNAc transferase 2	Homo sapiens (human)	congenital disorder of glycosylation type II
2591	polypeptide N-acetylgalactosaminyltransferase 3	GALNT3 Aliases: GalNAc-T3 HFTC HHS polypeptide GalNAc transferase 3	Homo sapiens (human)	hyperphosphatemic familial tumoral calcinosis
2629	glucosylceramidase beta 1	GBA1 Aliases: glucocerebrosidase	Homo sapiens (human)	Gaucher's disease perinatal lethal Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease type IIIC Gaucher's disease Lewy body dementia Parkinson's disease Parkinsonism late onset Parkinson's disease
2632	1,4-alpha-glucan branching enzyme 1	GBE1 Aliases: Andersen disease glycogen branching enzyme glycogen storage disease type IV	Homo sapiens (human)	glycogen storage disease IV pulmonary tuberculosis
2650	glucosaminyl (N-acetyl) transferase 1	GCNT1 Aliases: C2GNT NAGCT2 beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N--acetylglucosaminyltransferase core 2 beta1,6 N-acetylglucosaminyltransferase-I	Homo sapiens (human)
2651	glucosaminyl (N-acetyl) transferase 2 (I blood group)	GCNT2 Aliases: IGNT Ii blood group NAGCT1 ULG3 bA360O19.2 bA421M1.1 unassigned linkage group 3	Homo sapiens (human)	cataract 13 with adult i phenotype cataract
2683	beta-1,4-galactosyltransferase 1	B4GALT1 Aliases: Beta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase N-acetyllactosamine synthase beta4Gal-T1 lactose synthase A	Homo sapiens (human)	congenital disorder of glycosylation type IId congenital disorder of glycosylation
2992	glycogenin 1	GYG1 Aliases: glycogenin glucosyltransferase	Homo sapiens (human)	glycogen storage disease XV glycogen storage disease
2997	glycogen synthase 1	GYS1 Aliases: GSY	Homo sapiens (human)	cardiovascular system disease
2998	glycogen synthase 2	GYS2	Homo sapiens (human)	glycogen storage disease
3036	hyaluronan synthase 1	HAS1	Homo sapiens (human)
3037	hyaluronan synthase 2	HAS2	Homo sapiens (human)
3038	hyaluronan synthase 3	HAS3	Homo sapiens (human)
3073	hexosaminidase subunit alpha	HEXA Aliases: GM2 gangliosidosis Tay Sachs disease beta-hexosaminidase subunit alpha	Homo sapiens (human)	Tay-Sachs disease
3074	hexosaminidase subunit beta	HEXB Aliases: beta-hexosaminidase subunit beta	Homo sapiens (human)	Sandhoff disease spinal muscular atrophy
3251	hypoxanthine phosphoribosyltransferase 1	HPRT1 Aliases: HGPRT Lesch-Nyhan syndrome hypoxanthine guanine phosphoribosyl transferase	Homo sapiens (human)	HRPT-related hyperuricemia Lesch-Nyhan syndrome
3373	hyaluronidase 1	HYAL1 Aliases: HYAL-1 LUCA1	Homo sapiens (human)	mucopolysaccharidosis IX mucopolysaccharidosis
3703	STT3 oligosaccharyltransferase complex catalytic subunit A	STT3A Aliases: MGC9042 STT3-A TMC dolichyl-diphosphooligosaccharide protein glycotransferase	Homo sapiens (human)	congenital disorder of glycosylation Iw
3906	lactalbumin alpha	LALBA Aliases: HAMLET LYZG LYZL7 lactose synthase B lysozyme G	Homo sapiens (human)
3955	LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	LFNG Aliases: SCDO3	Homo sapiens (human)	spondylocostal dysostosis 3
4242	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	MFNG	Homo sapiens (human)
4245	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	MGAT1 Aliases: GLCNAC-TI GNT-1 GnTI	Homo sapiens (human)
4247	alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	MGAT2 Aliases: GNT-II	Homo sapiens (human)	congenital disorder of glycosylation type IIa
4248	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	MGAT3 Aliases: GNT-III	Homo sapiens (human)

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