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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

Displaying entries **26 - 50** of **423164** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
351	amyloid beta precursor protein	APP	Homo sapiens (human)	APP-related cerebral amyloid angiopathy Alzheimer's disease 1 Alzheimer's disease cognitive disorder traumatic brain injury
4851	notch receptor 1	NOTCH1	Homo sapiens (human)	Adams-Oliver syndrome adult T-cell leukemia/lymphoma aortic valve disease 1 congenital heart disease
57514	Rho GTPase activating protein 31	ARHGAP31	Homo sapiens (human)	Adams-Oliver syndrome coronary artery disease
3516	recombination signal binding protein for immunoglobulin kappa J region	RBPJ	Homo sapiens (human)	Adams-Oliver syndrome dilated cardiomyopathy
54567	delta like canonical Notch ligand 4	DLL4	Homo sapiens (human)	Adams-Oliver syndrome limb ischemia
57572	dedicator of cytokinesis 6	DOCK6	Homo sapiens (human)	Adams-Oliver syndrome
54485	delta like canonical Notch ligand 4	Dll4	Mus musculus (house mouse)	Adams-Oliver syndrome
285203	EGF domain specific O-linked N-acetylglucosamine transferase	EOGT Aliases: AER61 AER61 glycosyltransferase FLJ33770	Homo sapiens (human)	Adams-Oliver syndrome
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
3119	major histocompatibility complex, class II, DQ beta 1	HLA-DQB1	Homo sapiens (human)	Addison's disease Behcet's disease Creutzfeldt-Jakob disease Crohn's disease Graves' disease HTLV-1-associated myelopathy/tropical spastic paraparesis IgA glomerulonephritis Plasmodium falciparum malaria Sjogren's syndrome Stevens-Johnson syndrome Vogt-Koyanagi-Harada disease achalasia acute disseminated encephalomyelitis acute lymphoblastic leukemia acute myeloid leukemia agranulocytosis allergic bronchopulmonary aspergillosis allergic disease alopecia areata alveolar echinococcosis ankylosing spondylitis antiphospholipid syndrome aplastic anemia arthritis aspirin-induced respiratory disease asthma atrophic gastritis autoimmune disease autoimmune hepatitis autoimmune pancreatitis autoimmune polyendocrine syndrome type 2 autoimmune polyendocrine syndrome autoimmune thrombocytopenic purpura autoimmune thyroiditis bacterial infectious disease beta thalassemia celiac disease cervical cancer cervical dystonia chikungunya choreatic disease chronic myeloid leukemia cicatricial pemphigoid colorectal cancer common variable immunodeficiency common wart cystic echinococcosis degenerative myopia dental caries diabetic retinopathy dilated cardiomyopathy 1H dilated cardiomyopathy erythema multiforme glaucoma hepatitis B hepatitis C hepatocellular carcinoma human immunodeficiency virus infectious disease hyperthyroidism hypothyroidism immunoglobulin alpha deficiency iridocyclitis juvenile rheumatoid arthritis latex allergy liver cirrhosis marginal zone lymphoma multidrug-resistant tuberculosis multiple sclerosis myasthenia gravis mycosis fungoides myocarditis myositis narcolepsy neuromyelitis optica optic neuritis osteomyelitis paroxysmal nocturnal hemoglobinuria pemphigus vulgaris pemphigus pneumoconiosis pre-eclampsia primary progressive multiple sclerosis primary sclerosing cholangitis psoriasis pulmonary tuberculosis pure red-cell aplasia rheumatic fever rheumatic heart disease rheumatoid arthritis rhinitis rhinoscleroma sarcoidosis sickle cell anemia silicosis stomach disease systemic lupus erythematosus thrombotic thrombocytopenic purpura tuberculosis type 1 diabetes mellitus typhoid fever ulcerative colitis vitiligo vulva cancer
4261	class II major histocompatibility complex transactivator	CIITA	Homo sapiens (human)	Addison's disease MHC class II deficiency juvenile rheumatoid arthritis multiple sclerosis myocardial infarction rheumatoid arthritis systemic lupus erythematosus
23274	C-type lectin domain containing 16A	CLEC16A Aliases: Gop-1	Homo sapiens (human)	Addison's disease multiple sclerosis rheumatoid arthritis type 1 diabetes mellitus
25939	SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1	SAMHD1 Aliases: AGS5 Aicardi-Goutieres syndrome 5 HD domain containing 1 HDDC1 MOP-5 Mg11 SBBI88 monocyte protein 5	Homo sapiens (human)	Aicardi-Goutieres syndrome Chilblain lupus acute myeloid leukemia hepatitis B hepatitis C
103	adenosine deaminase RNA specific	ADAR Aliases: ADAR1 DRADA Double-stranded RNA-specific adenosine deaminase	Homo sapiens (human)	Aicardi-Goutieres syndrome Human papillomavirus infectious disease dyschromatosis symmetrica hereditaria liver cirrhosis
56417	adenosine deaminase, RNA-specific	Adar	Mus musculus (house mouse)	Aicardi-Goutieres syndrome
182	jagged canonical Notch ligand 1	JAG1	Homo sapiens (human)	Alagille syndrome Charcot-Marie-Tooth disease congenital heart disease multiple sclerosis tetralogy of Fallot
4853	notch receptor 2	NOTCH2	Homo sapiens (human)	Alagille syndrome Hajdu-Cheney syndrome
16449	jagged 1	Jag1	Mus musculus (house mouse)	Alagille syndrome
778	calcium voltage-gated channel subunit alpha1 F	CACNA1F	Homo sapiens (human)	Aland Island eye disease X-linked cone-rod dystrophy 3 congenital stationary night blindness 2A congenital stationary night blindness
14580	glial fibrillary acidic protein	Gfap	Mus musculus (house mouse)	Alexander disease
2670	glial fibrillary acidic protein	GFAP	Homo sapiens (human)	Alexander disease
84162	bridge-like lipid transfer protein family member 1	BLTP1	Homo sapiens (human)	Alkuraya-Kucinskas syndrome
1287	collagen type IV alpha 5 chain	COL4A5	Homo sapiens (human)	Alport syndrome X-linked Alport syndrome
1285	collagen type IV alpha 3 chain	COL4A3	Homo sapiens (human)	Alport syndrome autosomal dominant Alport syndrome autosomal recessive Alport syndrome benign familial hematuria end stage renal disease
236266	ALMS1, centrosome and basal body associated	Alms1	Mus musculus (house mouse)	Alstrom syndrome obesity

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