GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **3776 - 3800** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
115908	collagen triple helix repeat containing 1	CTHRC1
1277	collagen type I alpha 1 chain	COL1A1
1278	collagen type I alpha 2 chain	COL1A2
1280	collagen type II alpha 1 chain	COL2A1
1281	collagen type III alpha 1 chain	COL3A1
1282	collagen type IV alpha 1 chain	COL4A1
1284	collagen type IV alpha 2 chain	COL4A2
1285	collagen type IV alpha 3 chain	COL4A3
1286	collagen type IV alpha 4 chain	COL4A4
1287	collagen type IV alpha 5 chain	COL4A5
1288	collagen type IV alpha 6 chain	COL4A6
1297	collagen type IX alpha 1 chain	COL9A1
1298	collagen type IX alpha 2 chain	COL9A2 MED	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
1299	collagen type IX alpha 3 chain	COL9A3
1289	collagen type V alpha 1 chain	COL5A1
1290	collagen type V alpha 2 chain	COL5A2
50509	collagen type V alpha 3 chain	COL5A3
1291	collagen type VI alpha 1 chain	COL6A1	Bethlem myopathy Ullrich congenital muscular dystrophy congenital muscular dystrophy muscular dystrophy
1292	collagen type VI alpha 2 chain	COL6A2
1293	collagen type VI alpha 3 chain	COL6A3
256076	collagen type VI alpha 5 chain	COL6A5
131873	collagen type VI alpha 6 chain	COL6A6
1294	collagen type VII alpha 1 chain	COL7A1
1295	collagen type VIII alpha 1 chain	COL8A1
1296	collagen type VIII alpha 2 chain	COL8A2

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