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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 **1 - 25** of **13418** 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
3123	major histocompatibility complex, class II, DR beta 1	HLA-DRB1	Homo sapiens (human)	Addison's disease Alport syndrome Alzheimer's disease Behcet's disease Chagas disease Graves' disease Hantavirus hemorrhagic fever with renal syndrome Human papillomavirus infectious disease Meniere's disease Parkinson's disease Sjogren's syndrome Takayasu's arteritis Vogt-Koyanagi-Harada disease abdominal aortic aneurysm acute disseminated encephalomyelitis allergic asthma allergic bronchopulmonary aspergillosis allergic disease alveolar echinococcosis ankylosing spondylitis anti-basement membrane glomerulonephritis antiphospholipid syndrome aspirin-induced respiratory disease asthma atrophic gastritis autistic disorder autoimmune disease autoimmune hepatitis autoimmune polyendocrine syndrome type 2 autoimmune polyendocrine syndrome autoimmune thrombocytopenic purpura autoimmune thyroiditis bacterial infectious disease breast cancer breast carcinoma celiac disease cerebral infarction cervix uteri carcinoma in situ choreatic disease cicatricial pemphigoid cystic echinococcosis diabetic angiopathy diabetic retinopathy endometriosis glaucoma hepatitis C human immunodeficiency virus infectious disease hypothyroidism idiopathic pulmonary fibrosis infectious mononucleosis juvenile rheumatoid arthritis latex allergy leprosy liver cirrhosis lupus nephritis mixed connective tissue disease multidrug-resistant tuberculosis multiple sclerosis myasthenia gravis myositis narcolepsy neuromyelitis optica optic neuritis paracoccidioidomycosis pemphigus peptic ulcer disease polyneuropathy primary progressive multiple sclerosis prostate cancer pulmonary sarcoidosis pulmonary tuberculosis pure red-cell aplasia renal cell carcinoma retinopathy of prematurity rheumatic fever rheumatic heart disease rheumatoid arthritis sarcoidosis schistosomiasis sensorineural hearing loss severe acute respiratory syndrome sympathetic ophthalmia systemic lupus erythematosus temporal arteritis thromboangiitis obliterans tuberculosis type 1 diabetes mellitus typhoid fever urticaria uveitis uveoparotid fever vitiligo vulva cancer
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
3558	interleukin 2	IL2	Homo sapiens (human)	Alzheimer's disease Behcet's disease Graves ophthalmopathy Graves' disease Takayasu's arteritis alopecia areata asthma ataxia telangiectasia atopic dermatitis autoimmune thrombocytopenic purpura bullous pemphigoid cholesteatoma of middle ear drug allergy graft-versus-host disease head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma interstitial lung disease limited scleroderma oral squamous cell carcinoma pancreatic cancer pemphigus primary immunodeficiency disease renal cell carcinoma rheumatoid arthritis rhinitis sensorineural hearing loss squamous cell carcinoma systemic lupus erythematosus type 1 diabetes mellitus urinary bladder cancer viral hepatitis
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
811	calreticulin	CALR Aliases: CRT FLJ26680 RO SSA Sicca syndrome antigen A (autoantigen Ro; calreticulin) autoantigen Ro cC1qR calregulin	Homo sapiens (human)	Burkitt lymphoma colon cancer colon carcinoma esophagus squamous cell carcinoma essential thrombocythemia hepatocellular carcinoma lung adenocarcinoma lung cancer myelofibrosis neuroendocrine tumor pancreatic ductal adenocarcinoma sideroblastic anemia thrombocytosis
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
7448	vitronectin	VTN	Homo sapiens (human)	Churg-Strauss syndrome granulomatosis with polyangiitis thrombosis
1272	contactin 1	CNTN1 Aliases: F3 GP135 glycoprotein gP135	Homo sapiens (human)	Compton-North congenital myopathy
12805	contactin 1	Cntn1	Mus musculus (house mouse)	Compton-North congenital myopathy
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
6402	selectin L	SELL Aliases: CD62L LAM-1 LAM1 LSEL Leu-8 Lyam-1 PLNHR hLHRc	Homo sapiens (human)	Crohn's disease IgA glomerulonephritis ulcerative colitis
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
329872	Fras1 related extracellular matrix protein 1	Frem1	Mus musculus (house mouse)	Fraser syndrome chromosome 9p deletion syndrome congenital diaphragmatic hernia
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
721	complement C4B (Chido/Rodgers blood group)	C4B	Homo sapiens (human)	Graves' disease autistic disorder complement component 4b deficiency renal cell carcinoma rheumatoid arthritis systemic lupus erythematosus
22914	killer cell lectin like receptor K1	KLRK1 Aliases: CD314 KLR NKG2-D NKG2D	Homo sapiens (human)	HTLV-1-associated myelopathy/tropical spastic paraparesis
6401	selectin E	SELE Aliases: CD62E ESEL	Homo sapiens (human)	IgA glomerulonephritis brain ischemia cerebrovascular disease coronary artery disease
3848	keratin 1	KRT1	Homo sapiens (human)	KRT1-related nonepidermolytic palmoplantar keratoderma epidermolytic hyperkeratosis 1 epidermolytic hyperkeratosis epidermolytic palmoplantar keratoderma 2 keratosis palmoplantaris striata 3
13853	epilepsy, progressive myoclonic epilepsy, type 2 gene alpha	Epm2a	Mus musculus (house mouse)	Lafora disease
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
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
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

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