GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q11206	CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 4	ST3GAL4 CGS23 NANTA3 SIAT4C STZ	5	4	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 Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenoid cystic carcinoma alopecia amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant intellectual developmental disorder 4 autosomal dominant intellectual developmental disorder 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 brain stem infarction campomelic dysplasia cancer carcinoma cardiomyopathy cataract cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis craniometaphyseal dysplasia dementia depressive disorder diabetes mellitus diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism distal myopathy dysthymic disorder embryoma encephalitis encephalomyelitis endomyocardial fibrosis essential hypertension facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial hyperlipidemia frontotemporal dementia gallbladder disease gestational diabetes granuloma annulare hepatocellular carcinoma hyperglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hypoglycemia large intestine cancer limb-girdle muscular dystrophy liver cancer liver disease major depressive disorder melancholic depression melanoma mucopolysaccharidosis IV mucopolysaccharidosis IVA muscular dystrophy myelitis myocardial infarction neuropathy neurotic disorder nonpapillary renal cell carcinoma 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 obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy osteoporosis pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peripheral nervous system disease polyneuropathy renal carcinoma renal cell carcinoma renal osteodystrophy retinal disease retinitis retrograde amnesia salivary gland adenoid cystic carcinoma salivary gland cancer sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease thrombophilia tongue squamous cell carcinoma 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
Q6UWI2	Prostate androgen-regulated mucin-like protein 1	PARM1	6	4
O75063	Glycosaminoglycan xylosylkinase	FAM20B KIAA0475	2	4	Desbuquois dysplasia Ehlers-Danlos syndrome osteogenesis imperfecta parapsoriasis psoriasis pustulosis of palm and sole
O75197	Low-density lipoprotein receptor-related protein 5	LRP5 LR3 LRP7	8	4
Q12888	TP53-binding protein 1	TP53BP1	13	4
P24394	Interleukin-4 receptor subunit alpha	IL4R IL4RA	6	4
P07949	Proto-oncogene tyrosine-protein kinase receptor Ret	RET CDHF12 CDHR16 PTC	16	4
P40939	Trifunctional enzyme subunit alpha, mitochondrial	HADHA HADH	4	4	Barth syndrome HELLP syndrome Norum disease Reye syndrome Tangier disease X-linked dilated cardiomyopathy abetalipoproteinemia acquired immunodeficiency syndrome adult respiratory distress syndrome agnosia alpha 1-antitrypsin deficiency alternating exotropia amyotrophic lateral sclerosis arthritis arthropathy blindness breast cancer bronchus cancer bronchus carcinoma cancer cardiomyopathy carnitine palmitoyltransferase II deficiency cerebral infarction cerebrovascular disease cholestasis choreaacanthocytosis clubfoot cone-rod dystrophy congenital adrenal hyperplasia congenital stationary night blindness 1A congenital stationary night blindness congestive heart failure coronary artery disease cystinuria cytochrome-c oxidase deficiency disease developmental coordination disorder diabetes mellitus dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of metabolism endomyocardial fibrosis epilepsy exotropia familial hypertrophic cardiomyopathy familial periodic paralysis fibromyalgia fundus albipunctatus galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hemophagocytic lymphohistiocytosis hepatitis C human immunodeficiency virus infectious disease hypercalcemia hypertrophic cardiomyopathy hypoglycemia hypolipoproteinemia hypoparathyroidism inflammatory bowel disease inherited metabolic disorder intellectual disability lactic acidosis learning disability liver disease lung benign neoplasm lung cancer lung carcinoma metabolic dysfunction-associated steatotic liver disease mitochondrial trifunctional protein deficiency mitral valve insufficiency mitral valve prolapse monocular exotropia myoglobinuria myopathy myopia myositis nephrocalcinosis neuropathy newborn respiratory distress syndrome night blindness obesity obsolete asthenopia osteoarthritis peripheral nervous system disease phosphorus metabolism disease placental insufficiency polyneuropathy pre-eclampsia progressive muscular atrophy prostate cancer prostate carcinoma prostatitis pseudohypoparathyroidism pseudosarcomatous fibromatosis retinal disease retinitis pigmentosa retinitis sick sinus syndrome staphyloma posticum steatotic liver disease sudden infant death syndrome tricuspid valve insufficiency type 2 diabetes mellitus urea cycle disorder visual epilepsy von Willebrand's disease 2 von Willebrand's disease
P08670	Vimentin	VIM	29	4
Q9H251	Cadherin-23	CDH23 KIAA1774 KIAA1812	42	4
Q96M89	Coiled-coil domain-containing protein 138	CCDC138	2	4
P22607	Fibroblast growth factor receptor 3	FGFR3 JTK4	6	4
Q8TDX6	Chondroitin sulfate N-acetylgalactosaminyltransferase 1	CSGALNACT1 CHGN GALNACT1	5	4	Guillain-Barre syndrome Laron syndrome Miller Fisher syndrome achondroplasia anorexia nervosa breast cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer diabetic ketoacidosis large intestine cancer melanoma multiple sclerosis obsolete type 1 diabetes mellitus 9 skin melanoma 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
Q6KC79	Nipped-B-like protein	NIPBL IDN3 SCC2	18	4
P06744	Glucose-6-phosphate isomerase	GPI	3	4	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 Cockayne syndrome Cornelia de Lange syndrome Creutzfeldt-Jakob disease Down syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Pick's disease Plasmodium vivax malaria Prader-Willi syndrome Reye syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute myeloid leukemia acute myocardial infarction adult fibrosarcoma adult lymphoma alternating hemiplegia of childhood anemia antiphospholipid syndrome aplastic anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrophic gastritis atypical hemolytic-uremic syndrome autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome autonomic neuropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome benign mesothelioma blastomycosis bone osteosarcoma brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer central nervous system disease central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood leukemia childhood lymphoma childhood osteosarcoma cholecystitis chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma chronic fatigue syndrome chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common cold congenital diaphragmatic hernia congenital disorder of glycosylation congenital hemolytic anemia congenital nonspherocytic hemolytic anemia coronary artery disease coronary thrombosis cystinuria depressive disorder diabetes mellitus diabetic ketoacidosis differentiated thyroid gland carcinoma diffuse large B-cell lymphoma dysthymic disorder dystonia embryoma encephalitis encephalomyelitis endocarditis endometrial cancer endometrial carcinoma essential hypertension essential thrombocythemia familial retinoblastoma favism female stress incontinence fetal erythroblastosis fibrosarcoma focal hand dystonia galactosemia generalized dystonia giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease head and neck squamous cell carcinoma hematologic cancer hemoglobinopathy hemolytic anemia hemolytic-uremic syndrome hepatitis B hepatitis hepatocellular carcinoma hereditary elliptocytosis high grade glioma human immunodeficiency virus infectious disease hypertension immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease infective endocarditis inflammatory and toxic neuropathy influenza intellectual disability intracranial embolism large intestine cancer learning disability leukemia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lupus erythematosus lymphoma macrocytic anemia major depressive disorder malignant hyperthermia malignant mesothelioma melancholic depression microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microphthalmia migraine mixed glioma multiple sclerosis myelitis myelodysplastic syndrome myocardial infarction neonatal anemia neonatal jaundice nervous system disease neurogenic arthropathy neurotic disorder nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pancytopenia papillary adenocarcinoma papillary renal cell carcinoma paracoccidioidomycosis paroxysmal nocturnal hemoglobinuria peeling skin syndrome placental insufficiency platelet-type bleeding disorder 3 pre-eclampsia primary immunodeficiency disease primary pulmonary hypertension prion disease pure red-cell aplasia renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease retinoblastoma rheumatoid arthritis sarcomatoid renal cell carcinoma scleroderma silent myocardial infarction skin atrophy steatotic liver disease stomach cancer stomach carcinoma subacute bacterial endocarditis syndromic X-linked intellectual disability Snyder type syndromic intellectual disability synovitis systemic lupus erythematosus systemic scleroderma tenosynovitis thrombophilia thrombotic thrombocytopenic purpura thyroid gland anaplastic carcinoma thyroid gland papillary carcinoma trilateral retinoblastoma 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 uterine corpus cancer vascular dementia vascular disease viral infectious disease von Willebrand's disease
Q14773	Intercellular adhesion molecule 4	ICAM4 LW	6	4
Q9Y5G0	Protocadherin gamma-B5	PCDHGB5	2	4
Q709C8	Intermembrane lipid transfer protein VPS13C	VPS13C KIAA1421	2	4
Q9BZ95	Histone-lysine N-methyltransferase NSD3	NSD3 WHSC1L1	4	4
Q96JA1	Leucine-rich repeats and immunoglobulin-like domains protein 1	LRIG1 LIG1	12	4
Q9BVT8	Transmembrane and ubiquitin-like domain-containing protein 1	TMUB1 C7orf21 DULP HOPS	3	4
Q9UK76	Jupiter microtubule associated homolog 1	JPT1 ARM2 HN1	4	4
O75056	Syndecan-3	SDC3 KIAA0468	32	4	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 Creutzfeldt-Jakob disease Duchenne muscular dystrophy Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 breast fibrocystic disease cancer cerebral degeneration chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hepatitis C hepatocellular carcinoma liver cancer microglandular adenosis muscular dystrophy nonpapillary renal cell carcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma
P82987	ADAMTS-like protein 3	ADAMTSL3 KIAA1233	20	4
Q9P2E5	Chondroitin sulfate glucuronyltransferase	CHPF2 CHSY3 CSGLCAT KIAA1402	2	4	cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer

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