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 **2951 - 2975** 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
Q9BZZ2	Sialoadhesin	SIGLEC1 SN	Homo sapiens (human)	14	0	Ebola hemorrhagic fever Graves' disease Kaposi's sarcoma Marfan syndrome St. Louis encephalitis allergic asthma anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ascariasis ascaridiasis asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome bladder carcinoma breast cancer breast carcinoma cancer childhood leukemia chronic fatigue syndrome colitis common cold congenital heart block coronary artery disease diabetes mellitus embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma gastroenteritis glomerulonephritis head and neck squamous cell carcinoma hepatitis B hepatitis C hyperthyroidism ileitis ileocolitis immune system disease influenza intrinsic asthma kidney disease leukemia liver cirrhosis lupus erythematosus macrocytic anemia melanoma multiple myeloma multiple sclerosis myelitis nephritis nephrosis nutmeg liver prostate cancer prostate carcinoma pulmonary tuberculosis pyoureter respiratory syncytial virus infectious disease rheumatoid arthritis scleroderma situs inversus skin melanoma steatotic liver disease systemic lupus erythematosus systemic scleroderma thyrotoxicosis tuberculosis tuberculous pneumothorax tuberous sclerosis type 2 diabetes mellitus urinary bladder cancer viral infectious disease
Q6IA17	Single Ig IL-1-related receptor	SIGIRR	Homo sapiens (human)	4	0
Q8NBJ9	SID1 transmembrane family member 2	SIDT2	Homo sapiens (human)	11	8
Q9NXL6	SID1 transmembrane family member 1	SIDT1	Homo sapiens (human)	8	0
Q6IBE6	SIAT4C protein	SIAT4C ST3GAL4	Homo sapiens (human)	2	0
Q8IUQ4	E3 ubiquitin-protein ligase SIAH1	SIAH1 HUMSIAH	Homo sapiens (human)	1	1
Q9HAT2	Sialate O-acetylesterase	SIAE YSG2	Homo sapiens (human)	7	47
P14410	Sucrase-isomaltase, intestinal	SI	Homo sapiens (human)	18	3	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 Barrett's esophagus Clostridium difficile colitis Duchenne muscular dystrophy Fabry disease Gaucher's disease Gerstmann-Straussler-Scheinker syndrome Gorham's disease Japanese encephalitis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome adenocarcinoma adenoma amyotrophic lateral sclerosis arteriosclerotic cardiovascular disease atherosclerosis 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 brachydactyly type C brachydactyly cancer cardiomyopathy cardiovascular system disease cerebral degeneration chronic lymphocytic leukemia chylomicron retention disease colitis colorectal cancer colorectal carcinoma congenital disorder of glycosylation congenital muscular dystrophy coronary artery disease cribriform carcinoma cystic fibrosis cystinuria dengue disease depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism distal myopathy embryoma endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial periodic paralysis galactosemia gastric cardia adenocarcinoma gastroenteritis gastrointestinal system disease glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease granular cell carcinoma heart disease hyperglycemia hypertrophic cardiomyopathy hypoglycemia ileitis ileocolitis intestinal disease irritable bowel syndrome kwashiorkor lactose intolerance large intestine cancer limb-girdle muscular dystrophy lipid storage disease lysosomal storage disease major depressive disorder marasmus melancholic depression muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myotonic dystrophy type 1 myotonic dystrophy type 2 nephrolithiasis neurocirculatory asthenia neurodegenerative disease nutmeg liver nutrition disease obesity 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 melancholia oculopharyngeal muscular dystrophy peptic ulcer disease prediabetes syndrome progressive muscular atrophy prolactinoma protein-energy malnutrition punctate palmoplantar keratoderma type III rippling muscle disease 2 sudden infant death syndrome tropical sprue tubular adenocarcinoma type 2 diabetes mellitus uric acid nephrolithiasis viral infectious disease yellow fever
A0MZ66	Shootin-1	SHTN1 KIAA1598	Homo sapiens (human)	2	2
Q9ULL8	Protein Shroom4	SHROOM4 KIAA1202 SHAP	Homo sapiens (human)	0	1
Q8TF72	Protein Shroom3	SHROOM3 KIAA1481 SHRML	Homo sapiens (human)	0	1
Q149N8	E3 ubiquitin-protein ligase SHPRH	SHPRH KIAA2023	Homo sapiens (human)	0	1
Q9UQ13	Leucine-rich repeat protein SHOC-2	SHOC2 KIAA0862	Homo sapiens (human)	1	2
P34897	Serine hydroxymethyltransferase, mitochondrial	SHMT2	Homo sapiens (human)	0	1	B-cell lymphoma Down syndrome Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease anemia arthritis arthropathy autistic disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cholangiocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma gastrointestinal system cancer gliosarcoma head and neck squamous cell carcinoma hepatitis B hepatocellular carcinoma high grade glioma idiopathic interstitial pneumonia idiopathic pulmonary fibrosis intrahepatic cholangiocarcinoma large intestine cancer liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma macrocytic anemia mixed glioma neuroblastoma non-Hodgkin lymphoma obsolete ymphosarcoma osteoarthritis prostate cancer prostate carcinoma reticulosarcoma stomach cancer stomach carcinoma
Q3SXP7	Protein shisa-like-1	SHISAL1 KIAA1644	Homo sapiens (human)	2	0
B4DS77	Protein shisa-9	SHISA9	Homo sapiens (human)	4	2
B8ZZ34	Protein shisa-8	SHISA8 C22orf17	Homo sapiens (human)	1	0
A6NL88	Protein shisa-7	SHISA7	Homo sapiens (human)	4	1
Q6ZSJ9	Protein shisa-6	SHISA6	Homo sapiens (human)	3	2
Q8N114	Protein shisa-5	SHISA5 SCOTIN	Homo sapiens (human)	1	1
Q15465	Sonic hedgehog protein	SHH	Homo sapiens (human)	1	0
Q5VZ18	SH2 domain-containing adapter protein E	SHE	Homo sapiens (human)	1	1
Q92529	SHC-transforming protein 3	SHC3 NSHC SHCC	Homo sapiens (human)	0	1
P29353	SHC-transforming protein 1	SHC1 SHC SHCA	Homo sapiens (human)	1	2
A0A0C4DGN2	Sex hormone-binding globulin (Fragment)	SHBG	Homo sapiens (human)	2	0

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