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 **126201 - 126225** 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
Q6ZMP0	Thrombospondin type-1 domain-containing protein 4	THSD4	Homo sapiens (human)	23	42
P16671	Platelet glycoprotein 4	CD36 GP3B GP4	Homo sapiens (human)	13	42
P20851	C4b-binding protein beta chain	C4BPB	Homo sapiens (human)	8	42
P03951	Coagulation factor XI	F11	Homo sapiens (human)	5	43
P10586	Receptor-type tyrosine-protein phosphatase F	PTPRF LAR	Homo sapiens (human)	7	43
Q6P179	Endoplasmic reticulum aminopeptidase 2	ERAP2 LRAP	Homo sapiens (human)	10	43
P0DN86	Choriogonadotropin subunit beta 3	CGB3 CGB5 CGB8 CGB	Homo sapiens (human)	8	43
Q810U4	Neuronal cell adhesion molecule	Nrcam Kiaa0343	Mus musculus (house mouse)	17	43
P06280	Alpha-galactosidase A	GLA	Homo sapiens (human)	3	44	Fabry disease Gaucher's disease Goodpasture syndrome Horner's syndrome Laron syndrome Meckel syndrome Moyamoya disease Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Riley-Day syndrome Takayasu's arteritis X-linked agammaglobulinemia Zollinger-Ellison syndrome achondroplasia acquired hyperkeratosis acute myocardial infarction allergic asthma anemia angiokeratoma anhidrosis antithrombin III deficiency anxiety disorder arthritis arthropathy asthma atrial fibrillation atrioventricular block autosomal dominant polycystic kidney disease bacterial vaginosis breast cancer breast fibrocystic disease brucellosis cancer cardiomyopathy cardiovascular system disease cataract central nervous system origin vertigo cerebral infarction cerebrovascular disease chronic kidney disease chronic obstructive pulmonary disease chylomicron retention disease congenital hypogammaglobulinemia congestive heart failure corneal dystrophy coronary thrombosis cystinuria depressive disorder diabetes insipidus diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism dysthymic disorder elephantiasis endomyocardial fibrosis epilepsy erythromelalgia essential hypertension familial hyperlipidemia familial hypertrophic cardiomyopathy familial mediterranean fever familial nephrotic syndrome fibromyalgia galactosemia generalized anxiety disorder glaucoma glomerulonephritis 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 granulomatosis with polyangiitis heart disease hyperinsulinism hypertension hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy hypoglycemia hypohidrosis influenza inherited metabolic disorder interstitial nephritis intrinsic asthma keratosis follicularis kidney disease kidney failure late onset Parkinson's disease lipid storage disease lipoid nephrosis lung disease lymphedema lysosomal storage disease macrocytic anemia major depressive disorder melancholic depression mevalonic aciduria microglandular adenosis mitral valve insufficiency mitral valve prolapse mongolian spot multiple sclerosis myocardial infarction myositis nephritis nephrosis nephrotic syndrome neurohypophyseal diabetes insipidus neuropathy neurotic disorder obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive lung disease optic atrophy osteoarthritis papillary adenocarcinoma papillary renal cell carcinoma peripheral nervous system disease pneumonia polyarteritis nodosa polyneuropathy priapism protein C deficiency protein S deficiency proteinuria pseudoxanthoma elasticum pyelitis pyelonephritis pyoureter recurrent corneal erosion renal infectious disease sensorineural hearing loss sick sinus syndrome silent myocardial infarction sphingolipidosis thrombophilia thyroid gland papillary carcinoma transient cerebral ischemia tuberculosis 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 uremia vaginitis vascular disease vertebrobasilar insufficiency visual epilepsy vitamin K deficiency bleeding vulvitis vulvovaginal candidiasis vulvovaginitis
P52948	Nuclear pore complex protein Nup98-Nup96	NUP98 ADAR2	Homo sapiens (human)	110	44
Q16853	Amine oxidase [copper-containing] 3	AOC3 VAP1	Homo sapiens (human)	10	44
P02468	Laminin subunit gamma-1	Lamc1 Lamb-2 Lamc-1	Mus musculus (house mouse)	17	44
P48960	Adhesion G protein-coupled receptor E5	ADGRE5 CD97	Homo sapiens (human)	18	44
Q12913	Receptor-type tyrosine-protein phosphatase eta	PTPRJ DEP1	Homo sapiens (human)	47	44
Q13410	Butyrophilin subfamily 1 member A1	BTN1A1 BTN	Homo sapiens (human)	2	44
Q8IWU6	Extracellular sulfatase Sulf-1	SULF1 KIAA1077	Homo sapiens (human)	10	44	Marinesco-Sjogren syndrome acute pancreatitis adult hepatocellular carcinoma anal carcinoma in situ arthritis arthropathy bacterial sepsis bladder urothelial carcinoma brain cancer breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cervix uteri carcinoma in situ childhood hepatocellular carcinoma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma degenerative disc disease disease of metabolism embryoma giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatitis hepatocellular carcinoma high grade glioma idiopathic interstitial pneumonia large intestine cancer liver cancer liver carcinoma liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma nodular prostate osteoarthritis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pneumonia postinflammatory pulmonary fibrosis primary cerebellar degeneration prostatic adenoma pulmonary fibrosis seminoma skin melanoma steatotic liver disease stomach cancer stomach carcinoma testicular cancer testis seminoma transitional cell carcinoma
P04440	HLA class II histocompatibility antigen, DP beta 1 chain	HLA-DPB1 HLA-DP1B	Homo sapiens (human)	1	44
P19835	Bile salt-activated lipase	CEL BAL	Homo sapiens (human)	12	44	B-cell lymphoma Bloch-Sulzberger syndrome Goodpasture syndrome Loeffler syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Takayasu's arteritis Wolman disease X-linked chronic granulomatous disease acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute pancreatitis adamantinous craniopharyngioma adenocarcinoma adenoma adiposis dolorosa adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome aggressive systemic mastocytosis agranulocytosis alcoholic liver cirrhosis alcoholic pancreatitis allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma ataxic cerebral palsy atherosclerosis autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bacterial infectious disease bone marrow cancer brain disease breast cancer breast carcinoma bronchiectasis cancer central nervous system lymphoma childhood acute lymphocytic leukemia childhood lymphoma chronic eosinophilic leukemia chronic granulomatous disease chronic neutrophilic leukemia chronic obstructive pulmonary disease complement deficiency coronary artery disease craniopharyngioma cribriform carcinoma cutaneous porphyria cystic fibrosis cystic kidney disease diabetes mellitus diabetic ketoacidosis embryoma eosinophilic pneumonia epithelioid sarcoma erythropoietic protoporphyria exocrine pancreatic insufficiency extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue extrinsic allergic alveolitis familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial hyperlipidemia farmer's lung gastric lymphoma giardiasis glomerulonephritis granular cell carcinoma granulomatosis with polyangiitis hematologic cancer hepatitis C hepatitis hepatocellular carcinoma histoplasmosis hypereosinophilic syndrome hyperglycemia hyperinsulinemic hypoglycemia hypomelanosis of Ito idiopathic interstitial pneumonia idiopathic pulmonary fibrosis indolent systemic mastocytosis influenza interstitial lung disease intrinsic asthma kidney disease kwashiorkor leukopenia lipid storage disease lipomatosis liver cancer lung disease lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 lysosomal acid lipase deficiency malaria marasmus mastocytosis maturity-onset diabetes of the young type 8 maturity-onset diabetes of the young microphthalmia multiple symmetric lipomatosis myeloproliferative neoplasm nasopharynx carcinoma nephritis nephrosis neurofibromatosis 1 neurofibromatosis neutropenia newborn respiratory distress syndrome non-congenital cyst of kidney nutmeg liver nutrition disease obesity obsolete Matthew-Wood syndrome obsolete multiple symmetrical lipomatosis obsolete ymphosarcoma pancreas disease pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatitis papillary craniopharyngioma placental insufficiency plasmacytoma pneumocystosis pneumonia polyarteritis nodosa polycythemia vera polycythemia postinflammatory pulmonary fibrosis primary ciliary dyskinesia 1 primary ciliary dyskinesia protein-energy malnutrition pulmonary alveolar proteinosis pulmonary eosinophilia pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis pyoureter red-green color blindness retinal disease retinitis sarcoidosis sarcoma scleroderma severe congenital neutropenia spindle cell sarcoma steatotic liver disease substance abuse substance-related disorder systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic mastocytosis systemic scleroderma tuberculosis tuberculous pneumothorax tubular adenocarcinoma type 2 diabetes mellitus uveoparotid fever
P04925	Major prion protein	Prnp Prn-p Prp	Mus musculus (house mouse)	2	44
O95445	Apolipoprotein M	APOM G3A NG20	Homo sapiens (human)	1	44
Q8IVN8	Somatomedin-B and thrombospondin type-1 domain-containing protein	SBSPON C8orf84 RPESP	Homo sapiens (human)	1	45
O00469	Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2	PLOD2	Homo sapiens (human)	9	45	Bruck syndrome
Q86WC4	Osteopetrosis-associated transmembrane protein 1	OSTM1 GL	Homo sapiens (human)	11	45
P22413	Ectonucleotide pyrophosphatase/phosphodiesterase family member 1	ENPP1 M6S1 NPPS PC1 PDNP1	Homo sapiens (human)	10	45	Ehlers-Danlos syndrome HCL-V Laron syndrome McCune Albright syndrome X-linked dominant hypophosphatemic rickets Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne acquired hyperkeratosis acute myocardial infarction adult astrocytic tumor allergic asthma amelogenesis imperfecta anaplastic astrocytoma anemia angioid streaks ankylosing spondylitis ankylosis aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve stenosis arterial calcification of infancy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autosomal dominant hypophosphatemic rickets autosomal recessive hypophosphatemic rickets autosomal recessive osteopetrosis 7 bicuspid aortic valve disease bile duct adenocarcinoma bile duct cancer bile duct carcinoma bile duct disease blindness bone disease brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cardiovascular system disease carotid artery disease cartilage disease cerebral infarction cerebrovascular disease childhood astrocytic tumor childhood cerebral astrocytoma cholangiocarcinoma chondrocalcinosis chronic kidney disease colorectal cancer colorectal carcinoma congenital hypothyroidism congenital toxoplasmosis congestive heart failure connective tissue disease coronary artery disease coronary thrombosis craniosynostosis diabetes mellitus diabetic ketoacidosis embryoma encephalitis encephalomyelitis endometriosis of ovary endometriosis of uterus endometriosis enthesopathy essential hypertension exanthem fibrillary astrocytoma gemistocytic astrocytoma gestational diabetes giant cell glioblastoma glioblastoma glomerulonephritis glucose intolerance hairy cell leukemia heart disease hepatitis C hepatocellular carcinoma hereditary elliptocytosis herpes simplex high grade glioma hypercalcemia hypercementosis hyperglycemia hyperinsulinism hyperphosphatemic familial tumoral calcinosis hypertension hypophosphatemia hypothyroidism insulinoma intermittent claudication intrinsic asthma juvenile pilocytic astrocytoma keratosis follicularis kidney disease kidney failure large intestine cancer linear nevus sebaceous syndrome liver cancer lung benign neoplasm lung cancer lung carcinoma macrocytic anemia malignant astrocytoma melanoma mitral valve insufficiency mitral valve prolapse mongolian spot monoclonal gammopathy of uncertain significance morbid obesity mucopolysaccharidosis IV multiple epiphyseal dysplasia multiple myeloma musculoskeletal system disease myelitis myocardial infarction myopia myxedema nephritis nephrocalcinosis nephrosis neurogenic arthropathy nodular prostate nonepidermolytic palmoplantar keratoderma nutmeg liver obesity obsolete type 1 diabetes mellitus 9 ossification of the posterior longitudinal ligament of spine osteoarthritis osteochondrodysplasia osteogenesis imperfecta osteomalacia osteopetrosis osteoporosis osteosclerosis otitis media palmoplantar keratosis pancreatic cancer pancreatic carcinoma periarthritis perinatal intestinal perforation peripheral artery disease peripheral vascular disease phosphorus metabolism disease pilocytic astrocytoma plasmacytoma pneumocystosis polycystic ovary syndrome polycythemia vera polycythemia postural orthostatic tachycardia syndrome pre-eclampsia prediabetes syndrome prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma pseudoxanthoma elasticum pulmonary valve stenosis pyoureter restrictive cardiomyopathy retinal disease retinitis rheumatoid arthritis rickets sarcomatoid carcinoma scoliosis sensorineural hearing loss silent myocardial infarction skin melanoma spondyloarthropathy spondylosis steatotic liver disease subependymal giant cell astrocytoma suppurative periapical periodontitis tendinitis tropical sprue tympanosclerosis 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 uremia viral infectious disease
P10646	Tissue factor pathway inhibitor	TFPI LACI TFPI1	Homo sapiens (human)	9	45

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