GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P05997	Collagen alpha-2(V) chain	COL5A2	6	14
P25940	Collagen alpha-3(V) chain	COL5A3	8	9
P12109	Collagen alpha-1(VI) chain	COL6A1	7	82
A0A087X0S5	Collagen type VI alpha 1 chain (Fragment)	COL6A1	2	0
A0A384P5H7	Collagen, type VI, alpha 1, isoform CRA_b	COL6A1	2	0
P12110	Collagen alpha-2(VI) chain	COL6A2	9	116
P12111	Collagen alpha-3(VI) chain	COL6A3	26	97
A8TX70	Collagen alpha-5(VI) chain	COL6A5 COL29A1 VWA4	4	0
A6NMZ7	Collagen alpha-6(VI) chain	COL6A6	13	19
Q02388	Collagen alpha-1(VII) chain	COL7A1	7	2
P27658	Collagen alpha-1(VIII) chain	COL8A1 C3orf7	1	1
P25067	Collagen alpha-2(VIII) chain	COL8A2	3	1
P20849	Collagen alpha-1(IX) chain	COL9A1	2	1
Q14055	Collagen alpha-2(IX) chain	COL9A2	2	1	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
Q14050	Collagen alpha-3(IX) chain	COL9A3	1	0
Q9Y6Z7	Collectin-10	COLEC10 CLL1	2	1	3MC syndrome 3 3MC syndrome Klippel-Feil syndrome Laron syndrome Richter's syndrome achondroplasia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia allergic asthma asthma basal cell carcinoma blepharophimosis cancer carcinoma chronic lymphocytic leukemia cleft lip cleft palate cleidocranial dysplasia congenital ptosis craniosynostosis cryptorchidism essential thrombocythemia hepatocellular carcinoma humeroradial synostosis intellectual disability isolated cleft palate learning disability liver cancer lymphoblastic lymphoma lymphoplasmacytic lymphoma macroglobulinemia monoclonal gammopathy of uncertain significance multiple myeloma myelodysplastic syndrome obsolete lymphoplasmacytic lymphoma omphalocele ptosis radioulnar synostosis scoliosis sebaceous carcinoma sensorineural hearing loss spina bifida occulta spondylolisthesis sweat gland cancer umbilical hernia
Q5KU26	Collectin-12	COLEC12 CLP1 NSR2 SCARA4 SRCL	8	10	abdominal obesity-metabolic syndrome 1 arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis diabetes mellitus familial periodic paralysis multiple sclerosis myopathy substance abuse substance-related disorder type 2 diabetes mellitus
Q8NBJ5	Procollagen galactosyltransferase 1	COLGALT1 GLT25D1	5	31	Balo concentric sclerosis Simpson-Golabi-Behmel syndrome type 1 adrenoleukodystrophy bone osteosarcoma central nervous system disease cerebral degeneration childhood osteosarcoma epilepsy locked-in syndrome narcolepsy osteosarcoma porencephaly quadriplegia visual epilepsy
Q8IYK4	Procollagen galactosyltransferase 2	COLGALT2 C1orf17 GLT25D2 KIAA0584	4	6	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 Pick's disease Reye syndrome bone osteosarcoma breast cancer cerebral degeneration hepatitis A hepatitis lung benign neoplasm osteoarthritis osteosarcoma
Q9Y6G5	COMM domain-containing protein 10	COMMD10	0	1
Q86X83	COMM domain-containing protein 2	COMMD2	0	1
Q9UBI1	COMM domain-containing protein 3	COMMD3 BUP C10orf8	0	1
Q7Z4G1	COMM domain-containing protein 6	COMMD6	0	1
Q9P000	COMM domain-containing protein 9	COMMD9	0	1
P49747	Cartilage oligomeric matrix protein	COMP	3	19

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