GlyCosmos Portal

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 **326 - 350** 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
P07942	Laminin subunit beta-1	LAMB1	Homo sapiens (human)	18	135
Q14126	Desmoglein-2	DSG2 CDHF5	Homo sapiens (human)	18	85
Q8WXI9	Transcriptional repressor p66-beta	GATAD2B KIAA1150	Homo sapiens (human)	18	2
P18583	Protein SON	SON C21orf50 DBP5 KIAA1019 NREBP	Homo sapiens (human)	18	2
Q9BYF1	Angiotensin-converting enzyme 2	ACE2	Homo sapiens (human)	18	339
O15530	3-phosphoinositide-dependent protein kinase 1	PDPK1 PDK1	Homo sapiens (human)	18	1
P20930	Filaggrin	FLG	Homo sapiens (human)	18	1
O14639	Actin-binding LIM protein 1	ABLIM1 ABLIM KIAA0059 LIMAB1	Homo sapiens (human)	18	2
P49321	Nuclear autoantigenic sperm protein	NASP	Homo sapiens (human)	18	2
O75093	Slit homolog 1 protein	SLIT1 KIAA0813 MEGF4 SLIL1	Homo sapiens (human)	18	2
P21333	Filamin-A	FLNA FLN FLN1	Homo sapiens (human)	18	12
P08572	Collagen alpha-2(IV) chain	COL4A2	Homo sapiens (human)	18	6
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
O60469	Cell adhesion molecule DSCAM	DSCAM	Homo sapiens (human)	18	0
P48960	Adhesion G protein-coupled receptor E5	ADGRE5 CD97	Homo sapiens (human)	18	44
P20273	B-cell receptor CD22	CD22 SIGLEC2	Homo sapiens (human)	18	1	B-cell adult acute lymphocytic leukemia B-cell lymphoma Burkitt lymphoma CREST syndrome HCL-V Langerhans-cell histiocytosis Niemann-Pick disease type C1 Niemann-Pick disease Richter's syndrome T-cell acute lymphoblastic leukemia X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia abdominal aortic aneurysm acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma adult acute lymphocytic leukemia adult lymphoma arthritis arthropathy arthus reaction autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bacterial sepsis bone disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma bullous pemphigoid cancer capillary leak syndrome cartilage disease central nervous system lymphoma childhood B-cell acute lymphoblastic leukemia childhood acute lymphocytic leukemia childhood leukemia childhood lymphoma chronic lymphocytic leukemia collagen disease connective tissue disease diffuse large B-cell lymphoma disease of mental health embryoma enthesopathy essential thrombocythemia fibromyalgia giant cell glioblastoma glioblastoma hairy cell leukemia hematologic cancer hemolytic-uremic syndrome hepatic veno-occlusive disease hepatocellular carcinoma high grade glioma hypersensitivity reaction type III disease immune system disease interstitial lung disease leukemia limited scleroderma liver cancer lung benign neoplasm lung cancer lung carcinoma lymphoblastic lymphoma lymphoid leukemia lymphoma lymphoplasmacytic lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macroglobulinemia melanoma multiple myeloma myelodysplastic syndrome myeloid leukemia non-Hodgkin lymphoma obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma primary cutaneous T-cell non-Hodgkin lymphoma psychotic disorder refractory hairy cell leukemia reticulosarcoma rheumatoid arthritis scleroderma skin melanoma systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma vasculitis
P15144	Aminopeptidase N	ANPEP APN CD13 PEPN	Homo sapiens (human)	18	199
Q71U36	Tubulin alpha-1A chain	TUBA1A TUBA3	Homo sapiens (human)	18	2
Q9BQE3	Tubulin alpha-1C chain	TUBA1C TUBA6	Homo sapiens (human)	18	1
Q9Y678	Coatomer subunit gamma-1	COPG1 COPG	Homo sapiens (human)	18	1
Q8TEM1	Nuclear pore membrane glycoprotein 210	NUP210 KIAA0906	Homo sapiens (human)	18	23
P11388	DNA topoisomerase 2-alpha	TOP2A TOP2	Homo sapiens (human)	18	3
Q8NBJ4	Golgi membrane protein 1	GOLM1 C9orf155 GOLPH2	Homo sapiens (human)	18	61
Q9NZ53	Podocalyxin-like protein 2	PODXL2	Homo sapiens (human)	18	8
P11831	Serum response factor	SRF	Homo sapiens (human)	18	2

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