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 **876 - 900** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
Q0JA29	LRR receptor-like serine/threonine-protein kinase FLS2	FLS2	Oryza sativa Japonica Group (Japanese rice)	18	0
P23041	Major surface glycoprotein G	G	Human respiratory syncytial virus (subgroup B / strain 8/60)	18	0
P30005	120 kDa Glycoprotein O	U47 RF3/RF4	Human herpesvirus 6 (strain GS)	18	0
Q9BYF1	Angiotensin-converting enzyme 2	ACE2	Homo sapiens (human)	18	339
P32047	Protein MLF3	MLF3 YMK1	Saccharomyces cerevisiae S288C	18	1
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
Q5AND1	Maintenance of telomere capping protein 6	MTC6	Candida albicans SC5314	18	0
Q19791	A disintegrin and metalloproteinase with thrombospondin motifs gon-1	gon-1	Caenorhabditis elegans	18	0
P49321	Nuclear autoantigenic sperm protein	NASP	Homo sapiens (human)	18	2
F1NY98	Cell adhesion molecule DSCAM	DSCAM	Gallus gallus (chicken)	18	0
C0LGD7	Probable LRR receptor-like serine/threonine-protein kinase At1g06840	At1g06840	Arabidopsis thaliana (thale cress)	18	0
Q9C9H6	Receptor-like protein 11	RLP11	Arabidopsis thaliana (thale cress)	18	0
Q03497	Serine/threonine-protein kinase STE20	STE20	Saccharomyces cerevisiae S288C	18	1
Q9WU42	Nuclear receptor corepressor 2	Ncor2 Smrt	Mus musculus (house mouse)	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
F5HB53	Envelope glycoprotein B	gB	Human herpesvirus 5 strain Merlin	18	0
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
Q03656	Serine/threonine-protein kinase SKY1	SKY1	Saccharomyces cerevisiae S288C	18	1
Q9UTH5	Probable lysophospholipase C1786.02	SPAC1786.02	Schizosaccharomyces pombe 972h-	18	0
Q91A26	Spike glycoprotein	S	Bovine enteric coronavirus (strain 98TXSF-110-ENT)	18	0
Q9LJS0	Receptor-like protein 42	RLP42 RBPG1	Arabidopsis thaliana (thale cress)	18	0

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