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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 **9351 - 9375** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
1302	collagen type XI alpha 2 chain	COL11A2	Homo sapiens (human)
1301	collagen type XI alpha 1 chain	COL11A1	Homo sapiens (human)
1300	collagen type X alpha 1 chain	COL10A1	Homo sapiens (human)
1299	collagen type IX alpha 3 chain	COL9A3	Homo sapiens (human)
1298	collagen type IX alpha 2 chain	COL9A2 Aliases: MED	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Dowling-Degos disease Ehlers-Danlos syndrome Laron syndrome Laurin-Sandrow syndrome Osgood-Schlatter's disease Stickler syndrome achondroplasia acrodermatitis adult medulloblastoma allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia alternating hemiplegia of childhood amblyopia arthritis arthropathy asthma astigmatism atrial fibrillation autonomic neuropathy bone disease bone osteosarcoma cancer cardiovascular system disease cartilage disease cataract central nervous system cancer central nervous system disease childhood medulloblastoma childhood osteosarcoma chondrodysplasia punctata chronic kidney disease cleft palate collagen disease connective tissue disease degenerative disc disease depressive disorder dermatitis diabetes mellitus diastrophic dysplasia disease of metabolism dysplastic nevus syndrome dysthymic disorder epithelioid sarcoma essential hypertension eye disease familial hypercholesterolemia familial mediterranean fever familial periodic paralysis gliosarcoma granuloma annulare heart disease hemoglobin H disease high grade glioma hypertension intrinsic asthma isolated cleft palate major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma mevalonic aciduria mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia 2 multiple epiphyseal dysplasia myopathy myopia nervous system disease neurotic disorder obsolete melancholia osteoarthritis osteochondritis dissecans osteochondrodysplasia osteochondrosis osteogenesis imperfecta osteosarcoma pancreatic ductal adenocarcinoma pseudoachondroplasia reticulate acropigmentation of Kitamura retinal detachment rheumatoid arthritis sarcoma sensorineural hearing loss spinal stenosis spindle cell sarcoma strabismic amblyopia thalassemia thoracic aortic aneurysm type 2 diabetes mellitus
1297	collagen type IX alpha 1 chain	COL9A1	Homo sapiens (human)
1296	collagen type VIII alpha 2 chain	COL8A2	Homo sapiens (human)
1295	collagen type VIII alpha 1 chain	COL8A1	Homo sapiens (human)
1294	collagen type VII alpha 1 chain	COL7A1	Homo sapiens (human)
1293	collagen type VI alpha 3 chain	COL6A3	Homo sapiens (human)
1292	collagen type VI alpha 2 chain	COL6A2	Homo sapiens (human)
1291	collagen type VI alpha 1 chain	COL6A1	Homo sapiens (human)	Bethlem myopathy Ullrich congenital muscular dystrophy congenital muscular dystrophy muscular dystrophy
1290	collagen type V alpha 2 chain	COL5A2	Homo sapiens (human)
1289	collagen type V alpha 1 chain	COL5A1	Homo sapiens (human)
1288	collagen type IV alpha 6 chain	COL4A6	Homo sapiens (human)
1287	collagen type IV alpha 5 chain	COL4A5	Homo sapiens (human)
1286	collagen type IV alpha 4 chain	COL4A4	Homo sapiens (human)
1285	collagen type IV alpha 3 chain	COL4A3	Homo sapiens (human)
1284	collagen type IV alpha 2 chain	COL4A2	Homo sapiens (human)
1282	collagen type IV alpha 1 chain	COL4A1	Homo sapiens (human)
1281	collagen type III alpha 1 chain	COL3A1	Homo sapiens (human)
1280	collagen type II alpha 1 chain	COL2A1	Homo sapiens (human)
1278	collagen type I alpha 2 chain	COL1A2	Homo sapiens (human)
1277	collagen type I alpha 1 chain	COL1A1	Homo sapiens (human)
1272	contactin 1	CNTN1 Aliases: F3 GP135 glycoprotein gP135	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Compton-North congenital myopathy Guillain-Barre syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome adenocarcinoma adenoma arthritis arthropathy attention deficit hyperactivity disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy colorectal cancer colorectal carcinoma congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A craniosynostosis cribriform carcinoma embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis familial nephrotic syndrome familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome gliosarcoma granular cell carcinoma high grade glioma islet cell tumor large intestine cancer lipoid nephrosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma megaconial type congenital muscular dystrophy membranous glomerulonephritis mixed glioma multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myopathy nemaline myopathy nephrotic syndrome neuropathy peripheral nervous system disease placental insufficiency polyhydramnios polyneuropathy progressive muscular atrophy prostate cancer prostate carcinoma rigid spine muscular dystrophy 1 spinal muscular atrophy squamous cell carcinoma stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma tubular adenocarcinoma

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