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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 **76 - 100** of **13418** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
4126	mannosidase beta	MANBA Aliases: beta-mannosidase A	Homo sapiens (human)	beta-mannosidosis
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
4360	mannose receptor C-type 1	MRC1 Aliases: CD206 CLEC13D CLEC13DL bA541I19.1 macrophage mannose receptor	Homo sapiens (human)
4885	neuronal pentraxin 2	NPTX2	Homo sapiens (human)
4973	oxidized low density lipoprotein receptor 1	OLR1 Aliases: CLEC8A LOX-1 SCARE1	Homo sapiens (human)	cerebral amyloid angiopathy coronary artery disease myocardial infarction
5033	prolyl 4-hydroxylase subunit alpha 1	P4HA1	Homo sapiens (human)
5066	peptidylglycine alpha-amidating monooxygenase	PAM	Homo sapiens (human)
5167	ectonucleotide pyrophosphatase/phosphodiesterase 1	ENPP1 Aliases: PC-1 PCA1	Homo sapiens (human)	arterial calcification of infancy cardiovascular system disease end stage renal disease obesity ossification of the posterior longitudinal ligament of spine type 2 diabetes mellitus
5168	ectonucleotide pyrophosphatase/phosphodiesterase 2	ENPP2 Aliases: ATX PD-IALPHA autotaxin	Homo sapiens (human)
5211	phosphofructokinase, liver type	PFKL	Homo sapiens (human)
5213	phosphofructokinase, muscle	PFKM Aliases: PFK-1 PPP1R122 protein phosphatase 1, regulatory subunit 122	Homo sapiens (human)	glycogen storage disease VII
5214	phosphofructokinase, platelet	PFKP Aliases: PFK-C PFKF Phosphofructokinase, platelet type	Homo sapiens (human)
5310	polycystin 1, transient receptor potential channel interacting	PKD1 Aliases: PBP Pc-1 TRPP1 polycystin 1 transient receptor potential cation channel, subfamily P, member 1	Homo sapiens (human)	autosomal dominant polycystic kidney disease intracranial aneurysm polycystic kidney disease 1
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
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
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
5506	protein phosphatase 1 regulatory subunit 3A	PPP1R3A Aliases: GM glycogen-associated regulatory subunit of protein phosphatase-1 protein phosphatase 1 regulatory subunit GM	Homo sapiens (human)	hypoglycemia type 2 diabetes mellitus
5507	protein phosphatase 1 regulatory subunit 3C	PPP1R3C Aliases: PTG Phosphatase 1, regulatory inhibitor subunit 5 protein targeting to glycogen	Homo sapiens (human)
5509	protein phosphatase 1 regulatory subunit 3D	PPP1R3D	Homo sapiens (human)
5553	proteoglycan 2, pro eosinophil major basic protein	PRG2 Aliases: BMPG MBP eosinophil major basic protein proMBP	Homo sapiens (human)
5806	pentraxin 3	PTX3	Homo sapiens (human)	cystic fibrosis invasive aspergillosis
5818	nectin cell adhesion molecule 1	NECTIN1	Homo sapiens (human)	cleft lip-palate-ectodermal dysplasia syndrome cleft lip cleft palate ectodermal dysplasia
5836	glycogen phosphorylase L	PYGL Aliases: GSD6 Hers disease glycogen phosphorylase, liver form glycogen storage disease type VI	Homo sapiens (human)	glycogen storage disease VI glycogen storage disease lactic acidosis
5967	regenerating family member 1 alpha	REG1A	Homo sapiens (human)	type 1 diabetes mellitus
5968	regenerating family member 1 beta	REG1B Aliases: PSPS2 REGH REGI-BETA REGL lithostathine 1 beta secretory pancreatic stone protein 2	Homo sapiens (human)

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