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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 "carbohydrate binding"

Displaying entries **26 - 50** of **13418** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
1297	collagen type IX alpha 1 chain	COL9A1	Homo sapiens (human)	Stickler syndrome multiple epiphyseal dysplasia 6 osteochondrodysplasia
1462	versican	VCAN Aliases: PG-M versican proteoglycan	Homo sapiens (human)	intracranial aneurysm
1463	neurocan	NCAN Aliases: neurocan proteoglycan	Homo sapiens (human)
1621	dopamine beta-hydroxylase	DBH	Homo sapiens (human)	Parkinson's disease alcohol use disorder attention deficit hyperactivity disorder dopamine beta-hydroxylase deficiency hypertension migraine with aura
2022	endoglin	ENG	Homo sapiens (human)	arteriovenous malformation arteriovenous malformations of the brain breast cancer hereditary hemorrhagic telangiectasia intracranial aneurysm
2203	fructose-bisphosphatase 1	FBP1	Homo sapiens (human)	fructose-1,6-bisphosphatase deficiency
2208	Fc epsilon receptor II	FCER2 Aliases: C-type lectin domain family 4 member J CD23 CLEC4J FCErII Fc epsilon RII FcepsilonRII	Homo sapiens (human)
2219	ficolin 1	FCN1 Aliases: FCNM	Homo sapiens (human)
2220	ficolin 2	FCN2 Aliases: EBP-37 FCNL L-ficolin P35 collagen/fibrinogen domain-containing protein 2 ficolin B ficolin-2 hucolin serum lectin p35	Homo sapiens (human)
2539	glucose-6-phosphate dehydrogenase	G6PD Aliases: G6PD1	Homo sapiens (human)	Plasmodium falciparum malaria anemia cerebrovascular disease congenital nonspherocytic hemolytic anemia diabetes mellitus favism malaria neonatal jaundice
2548	alpha glucosidase	GAA Aliases: Pompe disease glycogen storage disease type II	Homo sapiens (human)	glycogen storage disease II
2584	galactokinase 1	GALK1	Homo sapiens (human)	cataract galactokinase deficiency
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
2595	glucosidase alpha, neutral C	GANC	Homo sapiens (human)
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
2645	glucokinase	GCK Aliases: HK4 hexokinase 4	Homo sapiens (human)	coronary artery disease diabetes mellitus familial hyperinsulinemic hypoglycemia 3 gestational diabetes hyperinsulinism hypertension hypoglycemia maturity-onset diabetes of the young type 2 permanent neonatal diabetes mellitus type 2 diabetes mellitus
2821	glucose-6-phosphate isomerase	GPI Aliases: AMF NLK	Homo sapiens (human)	congenital hemolytic anemia congenital nonspherocytic hemolytic anemia intellectual disability neuromuscular disease
2990	glucuronidase beta	GUSB	Homo sapiens (human)	mucopolysaccharidosis type VII
2997	glycogen synthase 1	GYS1 Aliases: GSY	Homo sapiens (human)	cardiovascular system disease
3098	hexokinase 1	HK1	Homo sapiens (human)	Charcot-Marie-Tooth disease type 4G acute lymphoblastic leukemia anemia congenital nonspherocytic hemolytic anemia multiple myeloma obesity retinitis pigmentosa
3099	hexokinase 2	HK2	Homo sapiens (human)	obesity type 2 diabetes mellitus
3101	hexokinase 3	HK3	Homo sapiens (human)
3122	major histocompatibility complex, class II, DR alpha	HLA-DRA	Homo sapiens (human)	Parkinson's disease allergic disease asthma autoimmune thyroiditis late onset Parkinson's disease multiple sclerosis

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