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 **1251 - 1275** 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
Q15154	Pericentriolar material 1 protein	PCM1	Homo sapiens (human)	4	5
P04264	Keratin, type II cytoskeletal 1	KRT1 KRTA	Homo sapiens (human)	7	5
O60716	Catenin delta-1	CTNND1 KIAA0384	Homo sapiens (human)	2	5
P54803	Galactocerebrosidase	GALC	Homo sapiens (human)	6	5	Evans' syndrome Fabry disease Farber lipogranulomatosis Gaucher's disease Krabbe disease Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wolman disease amblyopia autoimmune thrombocytopenic purpura bipolar disorder blindness bronchus cancer bronchus carcinoma cancer cerebellar ataxia cerebellar disease chronic obstructive pulmonary disease chylomicron retention disease communicating hydrocephalus congenital nystagmus demyelinating disease depressive disorder disease of metabolism dissociated nystagmus dysthymic disorder embryoma epilepsy glycogen storage disease II head and neck cancer head and neck squamous cell carcinoma hydrocephalus hypertropia inflammatory bowel disease laryngeal disease late onset Parkinson's disease leukodystrophy lipid storage disease low tension glaucoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lysosomal storage disease major depressive disorder mechanical strabismus melancholic depression metachromatic leukodystrophy multiple sclerosis nasopharynx carcinoma neurodegenerative disease neurotic disorder obsolete melancholia obstructive hydrocephalus ophthalmoplegia optic atrophy osteomalacia paraplegia pathologic nystagmus placental insufficiency primary open angle glaucoma relapsing fever rickets schizophrenia senile degeneration of brain sensorineural hearing loss sphingolipidosis spontaneous ocular nystagmus squamous cell carcinoma status epilepticus strabismic amblyopia strabismus systemic lupus erythematosus tongue squamous cell carcinoma tracheal disease visual epilepsy
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
Q9BRS8	La-related protein 6	LARP6	Homo sapiens (human)	1	5
Q6ZMH5	Zinc transporter ZIP5	SLC39A5 ZIP5	Homo sapiens (human)	6	5
Q8TDQ1	CMRF35-like molecule 1	CD300LF CD300F CLM1 IGSF13 IREM1 NKIR	Homo sapiens (human)	5	5
P78552	Interleukin-13 receptor subunit alpha-1	IL13RA1 IL13R IL13RA	Homo sapiens (human)	11	5
Q96CB8	Integrator complex subunit 12	INTS12 PHF22	Homo sapiens (human)	12	5
O43909	Exostosin-like 3	EXTL3 EXTL1L EXTR1 KIAA0519	Homo sapiens (human)	10	5	MHC class II deficiency acute myeloid leukemia adenosine deaminase deficiency agnosia arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 bacterial sepsis brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cherubism chondrodysplasia punctata ciliary body disease cocaine abuse cocaine dependence colorectal cancer colorectal carcinoma coronary artery disease developmental coordination disorder endometriosis of uterus endometriosis epithelioid sarcoma exostosis giant cell glioblastoma glioblastoma head and neck cancer head and neck squamous cell carcinoma hereditary multiple exostoses hypereosinophilic syndrome intellectual disability iris disease large intestine cancer learning disability liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphopenia morphine dependence mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIC mucopolysaccharidosis multiple epiphyseal dysplasia nutmeg liver osteochondrodysplasia osteopetrosis osteosclerosis panuveitis periarthritis pulmonary embolism sarcoma scoliosis secondary syphilis severe combined immunodeficiency spindle cell sarcoma tendinitis tuberculosis uveitis
O75077	Disintegrin and metalloproteinase domain-containing protein 23	ADAM23 MDC3	Homo sapiens (human)	9	5
P08887	Interleukin-6 receptor subunit alpha	IL6R	Homo sapiens (human)	10	5
Q9BVG9	Phosphatidylserine synthase 2	PTDSS2 PSS2	Homo sapiens (human)	1	5
P51587	Breast cancer type 2 susceptibility protein	BRCA2 FACD FANCD1	Homo sapiens (human)	2	5
P08319	All-trans-retinol dehydrogenase [NAD(+)] ADH4	ADH4 ADH2	Homo sapiens (human)	1	5	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease acute myeloid leukemia acute pancreatitis adenocarcinoma adenoma alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic pancreatitis anaplastic astrocytoma cancer carcinoma childhood cerebral astrocytoma cribriform carcinoma embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma fibrillary astrocytoma flat ductal epithelial atypia gemistocytic astrocytoma granular cell carcinoma hepatitis C hepatocellular carcinoma high grade glioma invasive ductal carcinoma juvenile pilocytic astrocytoma liver cancer liver cirrhosis malignant astrocytoma migraine ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pharynx cancer pilocytic astrocytoma protoplasmic astrocytoma squamous cell carcinoma squamous cell neoplasm steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma substance abuse substance-related disorder tongue squamous cell carcinoma tuberculosis tubular adenocarcinoma
Q7Z6B7	SLIT-ROBO Rho GTPase-activating protein 1	SRGAP1 ARHGAP13 KIAA1304	Homo sapiens (human)	7	5
Q6UXK5	Leucine-rich repeat neuronal protein 1	LRRN1 KIAA1497	Homo sapiens (human)	7	5
Q86YC3	Transforming growth factor beta activator LRRC33	NRROS LRRC33	Homo sapiens (human)	11	5
P14784	Interleukin-2 receptor subunit beta	IL2RB IL15RB	Homo sapiens (human)	4	5
Q9BXB1	Leucine-rich repeat-containing G-protein coupled receptor 4	LGR4 GPR48	Homo sapiens (human)	7	5
Q7Z417	FMR1-interacting protein NUFIP2	NUFIP2 KIAA1321	Homo sapiens (human)	21	5
Q9P2S2	Neurexin-2	NRXN2 KIAA0921	Homo sapiens (human)	8	5
Q5TCZ1	SH3 and PX domain-containing protein 2A	SH3PXD2A FISH KIAA0418 SH3MD1 TKS5	Homo sapiens (human)	5	5
P35443	Thrombospondin-4	THBS4 TSP4	Homo sapiens (human)	7	5

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