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 **5076 - 5100** of **18496** in total

« First

‹ Prev

…

200

201

202

203

204

205

206

207

208

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
A0A7I2V2E9	Angiotensin-converting enzyme	ACE2	Homo sapiens (human)	4	0
P40692	DNA mismatch repair protein Mlh1	MLH1 COCA2	Homo sapiens (human)	2	2
O76100	Olfactory receptor 7A10	OR7A10	Homo sapiens (human)	1	0
Q9BVC6	Voltage-gated monoatomic cation channel TMEM109	TMEM109	Homo sapiens (human)	1	1
Q8NDC0	MAPK-interacting and spindle-stabilizing protein-like	MAPK1IP1L C14orf32	Homo sapiens (human)	10	2
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
A0A0A7C4V2	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q96ME7	Zinc finger protein 512	ZNF512 KIAA1805	Homo sapiens (human)	2	1
A0A6B7FTT5	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q7Z2E3	Aprataxin	APTX AXA1	Homo sapiens (human)	1	1
Q9NZV1	Cysteine-rich motor neuron 1 protein	CRIM1 S52	Homo sapiens (human)	17	5
A0A0G2R0V5	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9P246	Stromal interaction molecule 2	STIM2 KIAA1482	Homo sapiens (human)	1	0
Q9GJM4	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A0A0A7C8J0	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q6UQM7	MHC class I antigen (Fragment)	HLA-Cw	Homo sapiens (human)	1	0
Q99500	Sphingosine 1-phosphate receptor 3	S1PR3 C9orf108 C9orf47 EDG3	Homo sapiens (human)	1	1
Q9TP26	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9Y5B0	RNA polymerase II subunit A C-terminal domain phosphatase	CTDP1 FCP1	Homo sapiens (human)	4	2
A0A1L2BMD4	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
O14757	Serine/threonine-protein kinase Chk1	CHEK1 CHK1	Homo sapiens (human)	1	1
Q13153	Serine/threonine-protein kinase PAK 1	PAK1	Homo sapiens (human)	1	0
Q8N7X4	Melanoma-associated antigen B6	MAGEB6	Homo sapiens (human)	2	2
Q63HM1	Kynurenine formamidase	AFMID	Homo sapiens (human)	0	1	colon cancer colonic benign neoplasm colorectal cancer large intestine cancer
O95866	Megakaryocyte and platelet inhibitory receptor G6b	MPIG6B C6orf25 G6B G6B-B	Homo sapiens (human)	2	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements