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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 "monosaccharide binding"

Displaying entries **1 - 25** of **4016** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
78989	collectin subfamily member 11	COLEC11 Aliases: CL-11 CL-K1 Collectin K1 MGC3279	Homo sapiens (human)	3MC syndrome 2
10584	collectin subfamily member 10	COLEC10 Aliases: CL-10 CL-L1	Homo sapiens (human)	3MC syndrome 3
4153	mannose binding lectin 2	MBL2	Homo sapiens (human)	Alzheimer's disease Behcet's disease Coronavirus infectious disease Crohn's disease Cryptococcal meningitis Kartagener syndrome Kawasaki disease Plasmodium falciparum malaria adult respiratory distress syndrome allergic bronchopulmonary aspergillosis aortic valve insufficiency asthma atopic dermatitis autoimmune thyroiditis bacterial infectious disease bacterial pneumonia bacterial vaginosis bipolar disorder bronchiolitis obliterans bronchopulmonary dysplasia chorioamnionitis chronic obstructive pulmonary disease common variable immunodeficiency coronary restenosis cryptosporidiosis cystic fibrosis dermatomyositis disease by infectious agent end stage renal disease fungal infectious disease hemolytic-uremic syndrome hepatitis B hepatitis C hepatocellular carcinoma herpes simplex human immunodeficiency virus infectious disease invasive aspergillosis lepromatous leprosy liver cirrhosis liver disease lung cancer lupus nephritis obesity otitis media ovarian cancer panic disorder peripheral vascular disease polymyalgia rheumatica psoriasis pulmonary fibrosis pulmonary tuberculosis respiratory allergy respiratory failure rhinitis sensorineural hearing loss systemic lupus erythematosus temporal arteritis thrombocytopenia toxic shock syndrome visceral leishmaniasis vitiligo vulvovaginal candidiasis
5352	procollagen-lysine,2-oxoglutarate 5-dioxygenase 2	PLOD2 Aliases: LH2 TLH lysyl hydroxlase 2 procollagen lysyl hydroxylase 2 telopeptidyl lysyl hydroxylase	Homo sapiens (human)	Bruck syndrome
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
30835	CD209 molecule	CD209 Aliases: CDSIGN CLEC4L DC-SIGN DC-SIGN1 hDC-SIGN	Homo sapiens (human)	Coronavirus infectious disease acquired immunodeficiency syndrome aspergillosis dengue disease dengue hemorrhagic fever extrapulmonary tuberculosis human immunodeficiency virus infectious disease pulmonary tuberculosis tuberculosis
5351	procollagen-lysine,2-oxoglutarate 5-dioxygenase 1	PLOD1 Aliases: LH1 lysyl hydroxlase 1 procollagen lysyl hydroxylase 1	Homo sapiens (human)	Ehlers-Danlos syndrome kyphoscoliotic type 1 brittle cornea syndrome 1
18822	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1	Plod1	Mus musculus (house mouse)	Ehlers-Danlos syndrome
5313	pyruvate kinase L/R	PKLR	Homo sapiens (human)	Gaucher's disease congenital nonspherocytic hemolytic anemia 2 congenital nonspherocytic hemolytic anemia malaria type 2 diabetes mellitus
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
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
25651	selectin P	Selp	Rattus norvegicus (Norway rat)	acute necrotizing pancreatitis anti-basement membrane glomerulonephritis
17159	mannosidase 2, alpha B1	Man2b1	Mus musculus (house mouse)	alpha-mannosidosis
2022	endoglin	ENG	Homo sapiens (human)	arteriovenous malformation arteriovenous malformations of the brain breast cancer hereditary hemorrhagic telangiectasia intracranial aneurysm
13805	endoglin	Eng	Mus musculus (house mouse)	arteriovenous malformations of the brain hereditary hemorrhagic telangiectasia
6403	selectin P	SELP Aliases: CD62 CD62P GMP140 PADGEM PSEL antigen CD62 granule membrane protein 140kDa	Homo sapiens (human)	atopic dermatitis myocardial infarction
81562	lectin, mannose binding 2 like	LMAN2L Aliases: DKFZp564L2423 VIP36-like VIPL	Homo sapiens (human)	autosomal dominant intellectual developmental disorder autosomal recessive intellectual developmental disorder 52
110173	mannosidase, beta A, lysosomal	Manba	Mus musculus (house mouse)	beta-mannosidosis
4126	mannosidase beta	MANBA Aliases: beta-mannosidase A	Homo sapiens (human)	beta-mannosidosis
3482	insulin like growth factor 2 receptor	IGF2R Aliases: CD222 CI-M6PR CI-MPR CIMPR M6P-R MPR1 MPR300 MPRI cation-independent mannose-6 phosphate receptor	Homo sapiens (human)	breast carcinoma in situ hepatocellular carcinoma in situ carcinoma nephroblastoma type 1 diabetes mellitus type 2 diabetes mellitus
6888	transaldolase 1	TALDO1	Homo sapiens (human)	carbohydrate metabolic disorder
2997	glycogen synthase 1	GYS1 Aliases: GSY	Homo sapiens (human)	cardiovascular system disease
2584	galactokinase 1	GALK1	Homo sapiens (human)	cataract galactokinase deficiency
24377	glucose-6-phosphate dehydrogenase	G6pd	Rattus norvegicus (Norway rat)	cataract transient cerebral ischemia
8813	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	DPM1 Aliases: CDGIE DPM synthase complex, catalytic subunit MPDS	Homo sapiens (human)	congenital disorder of glycosylation Ie

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