GlyCosmos Portal

GlyCosmos Glycoproteins

Integrated list of glycoproteins extracted from UniProt and annotated with glycosylation data from GlyGen, GlyConnect, GlycoProtDB and The O-GlcNAc Database. For each entry, information such as glycosylation site, glycans, diseases, 3D structures, and pathway information are available.

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 **1151 - 1175** 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
Q9P2D1	Chromodomain-helicase-DNA-binding protein 7	CHD7 KIAA1416	Homo sapiens (human)	8	3
Q6H9L7	Isthmin-2	ISM2 TAIL1 THSD3	Homo sapiens (human)	8	2
Q8N6Y1	Protocadherin-20	PCDH20 PCDH13	Homo sapiens (human)	8	2
Q99081	Transcription factor 12	TCF12 BHLHB20 HEB HTF4	Homo sapiens (human)	8	1
Q08554	Desmocollin-1	DSC1 CDHF1	Homo sapiens (human)	8	1
P26010	Integrin beta-7	ITGB7	Homo sapiens (human)	8	7
Q5JP69	Complement C2	C2	Homo sapiens (human)	8	0
Q12841	Follistatin-related protein 1	FSTL1 FRP	Homo sapiens (human)	8	27
O75144	ICOS ligand	ICOSLG B7H2 B7RP1 ICOSL KIAA0653	Homo sapiens (human)	8	11
P67809	Y-box-binding protein 1	YBX1 NSEP1 YB1	Homo sapiens (human)	8	2
P25940	Collagen alpha-3(V) chain	COL5A3	Homo sapiens (human)	8	9
P07225	Vitamin K-dependent protein S	PROS1 PROS	Homo sapiens (human)	8	5
Q8IZF6	Adhesion G-protein coupled receptor G4	ADGRG4 GPR112	Homo sapiens (human)	8	0
O75592	E3 ubiquitin-protein ligase MYCBP2	MYCBP2 KIAA0916 PAM	Homo sapiens (human)	8	3
Q93038	Tumor necrosis factor receptor superfamily member 25	TNFRSF25 APO3 DDR3 DR3 TNFRSF12 WSL WSL1	Homo sapiens (human)	8	1
Q8N8Z6	Discoidin, CUB and LCCL domain-containing protein 1	DCBLD1	Homo sapiens (human)	8	8
Q9UQD0	Sodium channel protein type 8 subunit alpha	SCN8A MED	Homo sapiens (human)	8	1
Q6UX71	Plexin domain-containing protein 2	PLXDC2 TEM7R	Homo sapiens (human)	8	30
Q99665	Interleukin-12 receptor subunit beta-2	IL12RB2	Homo sapiens (human)	8	0
P08949	Neuromedin-B	NMB	Homo sapiens (human)	8	1
Q01638	Interleukin-1 receptor-like 1	IL1RL1 DER4 ST2 T1	Homo sapiens (human)	8	11	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 Beckwith-Wiedemann syndrome CLOVES syndrome Cri-Du-Chat syndrome Crohn's colitis Crohn's disease Down syndrome Duchenne muscular dystrophy Graves' disease Japanese encephalitis Loeffler syndrome Perlman syndrome Pick's disease Reye syndrome Richter's syndrome Sotos syndrome Wolf-Hirschhorn syndrome acute leukemia acute lymphoblastic leukemia acute myeloid leukemia adult acute lymphocytic leukemia adult lymphoma allergic asthma allergic disease allergic rhinitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atopic dermatitis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis bacterial sepsis bronchiolitis bronchus cancer bronchus carcinoma cancer cardiomyopathy cardiovascular system disease central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood leukemia childhood lymphoma chorioamnionitis choroideremia chronic ethmoiditis chronic lymphocytic leukemia chronic obstructive pulmonary disease chronic sphenoidal sinusitis colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease craniosynostosis dengue disease dengue hemorrhagic fever dermatitis diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy endomyocardial fibrosis eosinophilic esophagitis eosinophilic pneumonia essential hypertension heart disease hepatitis B hepatoblastoma hepatocellular carcinoma hypereosinophilic syndrome hypertension hyperthyroidism hypertrophic cardiomyopathy idiopathic interstitial pneumonia immune system disease infantile histiocytoid cardiomyopathy inflammatory bowel disease 1 inflammatory bowel disease intestinal schistosomiasis intrinsic asthma large intestine cancer leprosy leukemia lung benign neoplasm lung cancer lung carcinoma lung disease lymphoma multiple myeloma muscular dystrophy nutmeg liver obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma pancreatic adenocarcinoma parasitic helminthiasis infectious disease peripheral artery disease postinflammatory pulmonary fibrosis pulmonary eosinophilia pulmonary fibrosis stomach cancer stomach carcinoma temporal arteritis thyrotoxicosis 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 ulcerative colitis ureteral obstruction vasomotor rhinitis viral infectious disease yellow fever
Q9NV96	Cell cycle control protein 50A	TMEM30A C6orf67 CDC50A	Homo sapiens (human)	8	36
P23142	Fibulin-1	FBLN1	Homo sapiens (human)	8	55
Q9Y286	Sialic acid-binding Ig-like lectin 7	SIGLEC7 AIRM1	Homo sapiens (human)	8	32	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 Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Guillain-Barre syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Marfan syndrome Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia Zollinger-Ellison syndrome acoustic neuroma acute biphenotypic leukemia acute leukemia acute myeloid leukemia adenosquamous carcinoma adult fibrosarcoma adult medulloblastoma agenesis of the corpus callosum with peripheral neuropathy allergic rhinitis alternating hemiplegia of childhood amyotrophic lateral sclerosis ankylosing spondylitis arthritis arthropathy atopic dermatitis atypical chronic myeloid leukemia, BCR-ABL1 negative autonomic neuropathy autosomal dominant familial periodic fever benign mesothelioma bipolar disorder bone marrow cancer brain stem infarction breast cancer breast carcinoma cancer cellular schwannoma central nervous system cancer central nervous system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease childhood medulloblastoma chordoma chronic lymphocytic leukemia chronic monocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy 2 cone-rod dystrophy delusional disorder depressive disorder dermatitis detrusor sphincter dyssynergia diabetes mellitus diabetic ketoacidosis dysthymic disorder eating disorder embryoma endometriosis of uterus endometriosis epilepsy esophagus squamous cell carcinoma familial combined hyperlipidemia familial hypercholesterolemia familial retinoblastoma fibrosarcoma gallbladder disease gangliocytoma ganglioneuroblastoma ganglioneuroma gastrinoma gastrointestinal system cancer gliosarcoma glomerulonephritis hepatitis hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 high grade glioma hyperglycemia hyperinsulinism kidney disease large intestine cancer laryngeal carcinoma larynx cancer leukemia liver disease lymphoid leukemia major depressive disorder malignant mesothelioma malignant peripheral nerve sheath tumor medulloblastoma medulloepithelioma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma melanotic neurilemmoma microphthalmia mixed glioma motor peripheral neuropathy myeloid leukemia myeloproliferative neoplasm nephritis nervous system disease neurilemmoma neuroblastoma neurodegenerative disease neuroectodermal tumor neurotic disorder obsolete Matthew-Wood syndrome obsolete T-cell lymphoblastic leukemia/lymphoma obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia osteoarthritis pancreatic ductal adenocarcinoma panic disorder paranoid schizophrenia plexiform schwannoma preretinal fibrosis progressive muscular atrophy prostate adenocarcinoma prostate cancer prostate carcinoma retinoblastoma rheumatoid arthritis rhinitis sick sinus syndrome situs inversus skin melanoma squamous cell carcinoma steatotic liver disease supratentorial primitive neuroectodermal tumor tendinitis tongue squamous cell carcinoma trilateral retinoblastoma tuberous sclerosis type 2 diabetes mellitus vasomotor rhinitis
P55317	Hepatocyte nuclear factor 3-alpha	FOXA1 HNF3A TCF3A	Homo sapiens (human)	8	1

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