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 **1851 - 1875** 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
Q13620	Cullin-4B	CUL4B KIAA0695	Homo sapiens (human)	10	3
P11216	Glycogen phosphorylase, brain form	PYGB	Homo sapiens (human)	2	3	acute myocardial infarction adenoid cystic carcinoma breast cancer cancer coronary artery disease coronary thrombosis diabetes mellitus embryoma lung cancer lung non-small cell carcinoma myocardial infarction salivary gland adenoid cystic carcinoma salivary gland cancer silent myocardial infarction type 2 diabetes mellitus
Q8WZ42	Titin	TTN	Homo sapiens (human)	22	3
Q8WUH6	Transmembrane protein 263	TMEM263 C12orf23	Homo sapiens (human)	10	3
P61221	ATP-binding cassette sub-family E member 1	ABCE1 RLI RNASEL1 RNASELI RNS4I	Homo sapiens (human)	1	3
P61513	Large ribosomal subunit protein eL43	RPL37A	Homo sapiens (human)	1	3
Q8N697	Solute carrier family 15 member 4	SLC15A4 PHT1 PTR4	Homo sapiens (human)	2	3
A8K979	ERI1 exoribonuclease 2	ERI2 EXOD1 KIAA1504	Homo sapiens (human)	2	3
Q658N2	Sialate:O-sulfotransferase 1	WSCD1 KIAA0523	Homo sapiens (human)	4	3
O60502	Protein O-GlcNAcase	OGA HEXC KIAA0679 MEA5 MGEA5	Homo sapiens (human)	5	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 Fabry disease GM1 gangliosidosis GM2 gangliosidosis, AB variant GM2 gangliosidosis Gaucher's disease Gilles de la Tourette syndrome Lewy body dementia Marfan syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sandhoff disease Tay-Sachs disease Timothy syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acute myocardial infarction alternating hemiplegia of childhood amnestic disorder amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis angiomatous meningioma anterior horn cell disease aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive distal hereditary motor neuronopathy 1 benign meningioma beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system disease cerebral convexity meningioma cerebral degeneration chronic kidney disease chylomicron retention disease clear cell meningioma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congestive heart failure connective tissue benign neoplasm coronary artery disease coronary thrombosis cystitis dermatitis diabetes mellitus diabetic ketoacidosis dystonia embryoma encephalitis encephalomyelitis epilepsy epithelioid sarcoma essential hypertension fibrous meningioma gangliosidosis gastroenteritis gastrointestinal system disease gestational diabetes giant cell glioblastoma gingivitis glioblastoma glomerulonephritis glucose intolerance glycoproteinosis heart disease hepatocellular carcinoma hydronephrosis hypertension ileitis ileocolitis intestinal disease intraorbital meningioma intraventricular meningioma kidney disease kidney failure kwashiorkor large intestine cancer lateral sclerosis lingual-facial-buccal dyskinesia lipid storage disease lipoid nephrosis liver cancer liver cirrhosis long QT syndrome 8 lung cancer lung carcinoma lymphoplasmacyte-rich meningioma lysosomal storage disease marasmus membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma microphthalmia motor neuron disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IVB mucopolysaccharidosis multiple acyl-CoA dehydrogenase deficiency multiple myeloma myelitis myocardial infarction nephritis nephrosis nervous system disease neurodegenerative disease nutrition disease obesity obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 olfactory groove meningioma ovarian cancer ovarian carcinoma panic disorder parasagittal meningioma pituitary adenoma prediabetes syndrome progressive familial intrahepatic cholestasis 1 progressive muscular atrophy progressive supranuclear palsy protein-energy malnutrition psammomatous meningioma pyoureter renal osteodystrophy retrograde amnesia sarcoma secondary Parkinson disease secretory meningioma silent myocardial infarction situs inversus sphingolipidosis spinal meningioma spindle cell sarcoma tauopathy thalassemia transitional meningioma tricuspid valve stenosis trigonitis 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 visual epilepsy
Q5SGD2	Protein phosphatase 1L	PPM1L PP2CE	Homo sapiens (human)	2	3
Q8N2Q7	Neuroligin-1	NLGN1 KIAA1070	Homo sapiens (human)	11	3
Q8IUL8	Cartilage intermediate layer protein 2	CILP2	Homo sapiens (human)	5	3
P11388	DNA topoisomerase 2-alpha	TOP2A TOP2	Homo sapiens (human)	18	3
Q86TE4	Leucine zipper protein 2	LUZP2	Homo sapiens (human)	4	3
P60709	Actin, cytoplasmic 1	ACTB	Homo sapiens (human)	8	3
Q96N46	Tetratricopeptide repeat protein 14	TTC14 KIAA1980	Homo sapiens (human)	7	3
O60938	Keratocan	KERA SLRR2B	Homo sapiens (human)	5	3
P80303	Nucleobindin-2	NUCB2 NEFA	Homo sapiens (human)	19	3
Q4KMG0	Cell adhesion molecule-related/down-regulated by oncogenes	CDON CDO	Homo sapiens (human)	12	3
Q8NI22	Multiple coagulation factor deficiency protein 2	MCFD2 SDNSF	Homo sapiens (human)	4	3	arteriosclerotic cardiovascular disease atherosclerosis blood coagulation disease cancer congenital afibrinogenemia congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia coronary artery disease embryoma factor V deficiency factor VII deficiency factor VIII deficiency hematopoietic system disease nutmeg liver obsolete inherited blood coagulation disease seminoma testicular cancer testicular germ cell cancer testis seminoma transient cerebral ischemia vertebrobasilar insufficiency vitamin K deficiency bleeding
Q6YBV0	Neutral amino acid uniporter 4	SLC36A4 PAT4	Homo sapiens (human)	3	3
Q8NHE4	V-type proton ATPase subunit e 2	ATP6V0E2 ATP6V0E2L C7orf32	Homo sapiens (human)	2	3
Q9HC07	Putative divalent cation/proton antiporter TMEM165	TMEM165 TPARL	Homo sapiens (human)	4	3	Camurati-Engelmann disease Laron syndrome Marfan syndrome X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 achondroplasia acoustic neuroma amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A amelogenesis imperfecta type 1B amelogenesis imperfecta type 1C amelogenesis imperfecta type 1E amelogenesis imperfecta type 1F amelogenesis imperfecta type 1G amelogenesis imperfecta type 1H amelogenesis imperfecta type 2A1 amelogenesis imperfecta type 3A amelogenesis imperfecta type 4 amelogenesis imperfecta cancer cellular schwannoma chondrodysplasia punctata congenital disorder of glycosylation type II congenital disorder of glycosylation type IIk congenital disorder of glycosylation dentin dysplasia dentinogenesis imperfecta embryoma hepatocellular carcinoma isolated elevated serum creatine phosphokinase levels liver cancer melanotic neurilemmoma meningioma neurilemmoma neurofibromatosis osteoporosis pituitary adenoma plexiform schwannoma scoliosis situs inversus tuberous sclerosis vestibular schwannomatosis
Q15303	Receptor tyrosine-protein kinase erbB-4	ERBB4 HER4	Homo sapiens (human)	11	3

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