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 **114701 - 114725** 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
Q4D0K8	Kinesin-like protein	Tc00.1047053508043.40	Trypanosoma cruzi strain CL Brener	0	1
Q9H347	Ubiquilin-3	UBQLN3	Homo sapiens (human)	1	1
Q9V9S7	Rho GTPase-activating protein 100F	RhoGAP100F Syd-1	Drosophila melanogaster (fruit fly)	0	1
Q5JRC9	Protein FAM47A	FAM47A	Homo sapiens (human)	1	1
Q8N9T8	Protein KRI1 homolog	KRI1	Homo sapiens (human)	2	1
Q498M7	CCR4-NOT transcription complex, subunit 4	Cnot4	Rattus norvegicus (Norway rat)	0	1
V5BCH2	Rac serine-threonine kinase	TCDM_08305	Trypanosoma cruzi Dm28c	0	1
P48147	Prolyl endopeptidase	PREP PEP	Homo sapiens (human)	0	1
P46783	Small ribosomal subunit protein eS10	RPS10	Homo sapiens (human)	0	1
Q9H7D7	WD repeat-containing protein 26	WDR26 CDW2 MIP2	Homo sapiens (human)	0	1
Q9UEY8	Gamma-adducin	ADD3 ADDL	Homo sapiens (human)	3	1
Q29980	MHC class I polypeptide-related sequence B	MICB PERB11.2	Homo sapiens (human)	6	1
P06493	Cyclin-dependent kinase 1	CDK1 CDC2 CDC28A CDKN1 P34CDC2	Homo sapiens (human)	0	1
P58742	Aladin	Aaas	Mus musculus (house mouse)	0	1
Q9QYY0	GRB2-associated-binding protein 1	Gab1	Mus musculus (house mouse)	12	1
Q9UBQ7	Glyoxylate reductase/hydroxypyruvate reductase	GRHPR GLXR	Homo sapiens (human)	1	1	atypical hemolytic-uremic syndrome calcinosis calcium metabolism disease chronic kidney disease hemolytic-uremic syndrome hypercalcemia kidney failure nephrocalcinosis nephrolithiasis phosphorus metabolism disease primary hyperoxaluria prostate cancer prostate carcinoma ureteral obstruction uric acid nephrolithiasis urinary tract obstruction
Q4CXJ7	Adenylosuccinate lyase	Tc00.1047053510337.30	Trypanosoma cruzi strain CL Brener	0	1
V5DCF9	Uncharacterized protein	TCDM_06643	Trypanosoma cruzi Dm28c	0	1
P07196	Neurofilament light polypeptide	NEFL NF68 NFL	Homo sapiens (human)	24	1
Q16445	Gamma-aminobutyric acid receptor subunit alpha-6	GABRA6	Homo sapiens (human)	3	1
Q9H871	E3 ubiquitin-protein transferase RMND5A	RMND5A	Homo sapiens (human)	0	1
P46467	Vacuolar protein sorting-associated protein 4B	Vps4b Skd1	Mus musculus (house mouse)	0	1
P11413	Glucose-6-phosphate 1-dehydrogenase	G6PD	Homo sapiens (human)	1	1	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 B-cell lymphoma Baraitser-Winter syndrome Bartter disease Bloch-Sulzberger syndrome Burkitt lymphoma Chagas disease Conn's syndrome Creutzfeldt-Jakob disease Duchenne muscular dystrophy Emery-Dreifuss muscular dystrophy Fabry disease Fraser syndrome Gilbert syndrome Goldenhar syndrome IGSF1 deficiency syndrome Japanese encephalitis Langerhans-cell histiocytosis Moebius syndrome Muenke Syndrome Nance-Horan syndrome Native American myopathy Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Plasmodium ovale malaria Plasmodium vivax malaria Renpenning syndrome Reye syndrome Richter's syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Waterhouse-Friderichsen syndrome Weissenbacher-Zweymuller syndrome Werner syndrome Wilson disease Wiskott-Aldrich syndrome X-linked chronic granulomatous disease abdominal obesity-metabolic syndrome 1 achromatopsia acoustic neuroma acquired color blindness acquired immunodeficiency syndrome acquired polycythemia acute chest syndrome acute kidney failure acute lymphoblastic leukemia acute megakaryocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenal adenoma adrenal cortex cancer adrenal gland cancer adrenoleukodystrophy adult acute lymphocytic leukemia adult hepatocellular carcinoma adult lymphoma age related macular degeneration allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia amyloidosis anaplastic astrocytoma anemia ankyloblepharon-ectodermal defects-cleft lip/palate syndrome anogenital venereal wart asthma ataxia telangiectasia atypical chronic myeloid leukemia, BCR-ABL1 negative atypical hemolytic-uremic syndrome autistic disorder bacterial sepsis beta thalassemia bilirubin metabolic disorder bipolar disorder bladder carcinoma blastomycosis blood group incompatibility blue color blindness bone marrow cancer borderline personality disorder brain cancer brain ischemia brain stem infarction branchiootic syndrome breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiac arrest cardiomyopathy cardiovascular system disease cataract central nervous system cancer central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood hepatocellular carcinoma childhood leukemia childhood lymphoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chromophobe renal cell carcinoma chronic granulomatous disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chylomicron retention disease classic galactosemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma common cold common wart conduct disorder cone-rod dystrophy congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia congenital hemolytic anemia congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nonspherocytic hemolytic anemia congestive heart failure contact dermatitis coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma cutaneous leishmaniasis cystinuria degeneration of macula and posterior pole dementia dengue disease dengue hemorrhagic fever diabetes mellitus diabetic ketoacidosis disease of mental health disease of metabolism duodenum cancer embryoma endocarditis endomyocardial fibrosis epilepsy epithelioid malignant peripheral nerve sheath tumor erythropoietin polycythemia esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia factor VIII deficiency familial adenomatous polyposis 1 familial adenomatous polyposis familial erythrocytosis 2 familial hyperlipidemia familial periodic paralysis favism fetal erythroblastosis fibrillary astrocytoma fragile X syndrome fundus albipunctatus galactokinase deficiency galactosemia gemistocytic astrocytoma gliosarcoma glomerulonephritis glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease granular cell carcinoma heart cancer heart disease hematologic cancer hematopoietic system disease hemochromatosis hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobin H disease hemoglobinopathy hemoglobinuria hemolytic anemia hemolytic-uremic syndrome hemophilia B hepatic coma hepatic encephalopathy hepatitis A hepatitis B hepatitis hepatoblastoma hepatocellular carcinoma hereditary elliptocytosis hereditary spherocytosis hidradenoma high grade glioma human immunodeficiency virus infectious disease hyperhomocysteinemia hyperparathyroidism hypertension hypertrophic cardiomyopathy hypohidrotic ectodermal dysplasia hypomelanosis of Ito hypothyroidism inherited metabolic disorder intellectual disability intermittent explosive disorder intrinsic asthma iron metabolism disease juvenile pilocytic astrocytoma kernicterus due to isoimmunization kernicterus kidney cancer kidney disease large intestine cancer learning disability leishmaniasis leukemia lingual-facial-buccal dyskinesia lipid storage disease liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma macrocytic anemia macular degeneration malaria malignant astrocytoma malignant peripheral nerve sheath tumor melanoma metabolic dysfunction-associated steatotic liver disease methemoglobinemia middle cerebral artery infarction mixed glioma movement disease mucocutaneous leishmaniasis multiple myeloma muscular dystrophy myelodysplastic syndrome myelofibrosis myeloid leukemia myeloproliferative neoplasm myocardial infarction myopathy myxedema neonatal jaundice nephritis nephrogenic diabetes insipidus nephrosis neurilemmoma neuroblastoma neurodegenerative disease neurofibromatosis 1 neurofibromatosis neurofibrosarcoma non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete subacute myeloid leukemia obsolete ymphosarcoma occupational dermatitis oculocerebrorenal syndrome orofaciodigital syndrome I orofaciodigital syndrome X osteitis fibrosa pancytopenia papillary adenocarcinoma papillary renal cell carcinoma paracoccidioidomycosis parathyroid adenoma parathyroid carcinoma paroxysmal nocturnal hemoglobinuria peroxisome biogenesis disorder 8A phagocyte bactericidal dysfunction phenylketonuria pheochromocytoma pilocytic astrocytoma plasmacytoma pneumocystosis polycythemia vera polycythemia prediabetes syndrome priapism primary hyperaldosteronism primary immunodeficiency disease primary pulmonary hypertension progeria prostate cancer prostate carcinoma protoplasmic astrocytoma psychotic disorder pterygium pyoureter pyruvate kinase deficiency of red cells red color blindness red-green color blindness renal carcinoma renal cell carcinoma renovascular hypertension reticulosarcoma retinitis pigmentosa rhabdomyosarcoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder senile cataract sickle cell anemia silent myocardial infarction skin melanoma skin papilloma skin tag small intestine cancer spondylocarpotarsal synostosis syndrome steatotic liver disease stress polycythemia subependymal giant cell astrocytoma sulfhemoglobinemia syringoma thalassemia thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma transient cerebral ischemia trypanosomiasis tubular adenocarcinoma 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 urinary bladder cancer vascular dementia vascular disease vertebrobasilar insufficiency viral infectious disease visceral leishmaniasis visual epilepsy vitiligo yellow fever
O54910	NF-kappa-B inhibitor epsilon	Nfkbie Ikbe	Mus musculus (house mouse)	0	1
Q13363	C-terminal-binding protein 1	CTBP1 CTBP	Homo sapiens (human)	0	1

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