GlyCosmos Portal

GlyCosmos Glycoproteins

Integrated list of glycoproteins extracted from UniProt and annotated with glycosylation data from GlyGen, GlyConnect, GlycoProtDB and The O-GlcNAc Database. For each entry, information such as glycosylation site, glycans, diseases, 3D structures, and pathway information are available.

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **501 - 525** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
P14314	Glucosidase 2 subunit beta	PRKCSH G19P1	Homo sapiens (human)	14	30	Marfan syndrome Meckel syndrome autosomal dominant polycystic kidney disease beta thalassemia breast cancer breast carcinoma cancer cerebellar ataxia, mental retardation and dysequlibrium syndrome cystic kidney disease diabetic ketoacidosis episodic ataxia type 2 esophagitis familial hemiplegic migraine 1 familial hemiplegic migraine familial hypercholesterolemia gallbladder disease gastroesophageal reflux disease hepatitis B hepatocellular carcinoma liver cancer liver disease non-congenital cyst of kidney obsolete type 1 diabetes mellitus 9 peptic esophagitis polycystic kidney disease 1 polycystic liver disease situs inversus tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus
P05546	Heparin cofactor 2	SERPIND1 HCF2	Homo sapiens (human)	14	66
Q8N307	Mucin-20	MUC20 KIAA1359	Homo sapiens (human)	14	2
Q15750	TGF-beta-activated kinase 1 and MAP3K7-binding protein 1	TAB1 MAP3K7IP1	Homo sapiens (human)	14	2
Q7Z5P9	Mucin-19	MUC19	Homo sapiens (human)	14	1
Q96JQ0	Protocadherin-16	DCHS1 CDH19 CDH25 FIB1 KIAA1773 PCDH16	Homo sapiens (human)	14	16
P34741	Syndecan-2	SDC2 HSPG1	Homo sapiens (human)	14	5	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 CST3-related cerebral amyloid angiopathy Duchenne muscular dystrophy Joubert syndrome Klatskin's tumor Marfan syndrome Miller-Dieker lissencephaly syndrome Pick's disease Reye syndrome adenocarcinoma adenoma adult fibrosarcoma ameloblastoma anthracosilicosis asbestosis autistic disorder autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy benign mesothelioma bone cancer bone osteosarcoma brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral amyloid angiopathy cerebral degeneration childhood osteosarcoma cholangiocarcinoma chondrosarcoma colitis colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy congestive heart failure diabetes mellitus diabetic ketoacidosis disease of mental health distal myopathy dysplastic nevus syndrome embryoma epidermolysis bullosa esophagus squamous cell carcinoma facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial hypercholesterolemia familial hyperlipidemia familial nephrotic syndrome fibrodysplasia ossificans progressiva fibrosarcoma follicular adenoma fragile X syndrome gallbladder cancer gallbladder carcinoma gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatitis B hepatitis C hepatocellular carcinoma hereditary multiple exostoses high grade glioma hydranencephaly hypereosinophilic syndrome hyperglycemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis interstitial nephritis intrahepatic cholangiocarcinoma kidney disease kidney failure large intestine cancer limb-girdle muscular dystrophy lipoid nephrosis lissencephaly liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lupus erythematosus lupus nephritis malignant mesothelioma melanoma membranous glomerulonephritis microcystic adenoma microphthalmia mixed glioma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myositis ossificans nephritis nephrosis nephrotic syndrome type 1 nephrotic syndrome obesity obsolete Matthew-Wood syndrome obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete hilar cholangiocellular carcinoma obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy osteosarcoma pancreatic adenocarcinoma papillary adenoma papillary carcinoma pneumonia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 postinflammatory pulmonary fibrosis proximal symphalangism psychotic disorder pulmonary fibrosis pyelitis pyelonephritis pyoureter renal infectious disease rheumatoid arthritis rippling muscle disease 2 scleroderma short-rib thoracic dysplasia 14 with polydactyly silicosis situs inversus skin melanoma skin squamous cell carcinoma squamous cell carcinoma syndromic X-linked intellectual disability Najm type systemic lupus erythematosus systemic scleroderma thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma tuberous sclerosis 1 tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus uremia
Q92859	Neogenin	NEO1 IGDCC2 NGN	Homo sapiens (human)	14	28
P06756	Integrin alpha-V	ITGAV MSK8 VNRA VTNR	Homo sapiens (human)	14	101
Q6ZU65	Ubinuclein-2	UBN2 KIAA2030	Homo sapiens (human)	14	1
Q99650	Oncostatin-M-specific receptor subunit beta	OSMR OSMRB	Homo sapiens (human)	14	24
Q8IXL6	Extracellular serine/threonine protein kinase FAM20C	FAM20C DMP4	Homo sapiens (human)	14	28
Q9NU53	Glycoprotein integral membrane protein 1	GINM1 C6orf72	Homo sapiens (human)	14	9
Q9UPZ6	Thrombospondin type-1 domain-containing protein 7A	THSD7A KIAA0960	Homo sapiens (human)	14	25
Q05586	Glutamate receptor ionotropic, NMDA 1	GRIN1 NMDAR1	Homo sapiens (human)	14	3
Q92896	Golgi apparatus protein 1	GLG1 CFR1 ESL1 MG160	Homo sapiens (human)	14	106
Q9UNA0	A disintegrin and metalloproteinase with thrombospondin motifs 5	ADAMTS5 ADAMTS11 ADMP2	Homo sapiens (human)	14	4
Q03001	Dystonin	DST BP230 BP240 BPAG1 DMH DT KIAA0728	Homo sapiens (human)	14	2
Q6UUV7	CREB-regulated transcription coactivator 3	CRTC3 TORC3	Homo sapiens (human)	14	4
Q13219	Pappalysin-1	PAPPA	Homo sapiens (human)	14	11
Q8NBS9	Thioredoxin domain-containing protein 5	TXNDC5 TLP46	Homo sapiens (human)	14	6
Q9NZN8	CCR4-NOT transcription complex subunit 2	CNOT2 CDC36 NOT2	Homo sapiens (human)	14	4
P10909	Clusterin	CLU APOJ CLI KUB1	Homo sapiens (human)	14	295
O00754	Lysosomal alpha-mannosidase	MAN2B1 LAMAN MANB	Homo sapiens (human)	14	63	IgA glomerulonephritis Klippel-Feil syndrome age related macular degeneration alpha-mannosidosis aspartylglucosaminuria cerebral degeneration congenital nystagmus degeneration of macula and posterior pole dissociated nystagmus fucosidosis gingival hypertrophy gingival overgrowth glycogen storage disease II hypertrichosis inguinal hernia intellectual disability learning disability lingual-facial-buccal dyskinesia lysosomal storage disease macular degeneration methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency movement disease mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis pathologic nystagmus retinal degeneration sensorineural hearing loss spondylolisthesis spontaneous ocular nystagmus
Q6N022	Teneurin-4	TENM4 KIAA1302 ODZ4 TNM4	Homo sapiens (human)	14	11

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