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 **124301 - 124325** of **126547** in total

« First

‹ Prev

…

4969

4970

4971

4972

4973

4974

4975

4976

4977

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
P24394	Interleukin-4 receptor subunit alpha	IL4R IL4RA	Homo sapiens (human)	6	4
P07949	Proto-oncogene tyrosine-protein kinase receptor Ret	RET CDHF12 CDHR16 PTC	Homo sapiens (human)	16	4
P40939	Trifunctional enzyme subunit alpha, mitochondrial	HADHA HADH	Homo sapiens (human)	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	Homo sapiens (human)	29	4
Q9H251	Cadherin-23	CDH23 KIAA1774 KIAA1812	Homo sapiens (human)	42	4
Q96M89	Coiled-coil domain-containing protein 138	CCDC138	Homo sapiens (human)	2	4
P48199	C-reactive protein	Crp Ptx1	Rattus norvegicus (Norway rat)	1	4
Q5SS00	DBF4-type zinc finger-containing protein 2 homolog	Zdbf2	Mus musculus (house mouse)	4	4
P22607	Fibroblast growth factor receptor 3	FGFR3 JTK4	Homo sapiens (human)	6	4
Q9CZ42	ATP-dependent (S)-NAD(P)H-hydrate dehydratase	Naxd Carkd	Mus musculus (house mouse)	2	4
Q8TDX6	Chondroitin sulfate N-acetylgalactosaminyltransferase 1	CSGALNACT1 CHGN GALNACT1	Homo sapiens (human)	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
Q6Q3F5	SID1 transmembrane family member 1	Sidt1	Rattus norvegicus (Norway rat)	7	4
O89026	Roundabout homolog 1	Robo1 Dutt1	Mus musculus (house mouse)	5	4
Q6KC79	Nipped-B-like protein	NIPBL IDN3 SCC2	Homo sapiens (human)	18	4
P62631	Elongation factor 1-alpha 2	Eef1a2 Eef1al Stn	Mus musculus (house mouse)	3	4
P06744	Glucose-6-phosphate isomerase	GPI	Homo sapiens (human)	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
Q6GQT6	Sterol regulatory element-binding protein cleavage-activating protein	Scap Kiaa0199	Mus musculus (house mouse)	3	4
Q61033	Lamina-associated polypeptide 2, isoforms alpha/zeta	Tmpo Lap2	Mus musculus (house mouse)	2	4
Q14773	Intercellular adhesion molecule 4	ICAM4 LW	Homo sapiens (human)	6	4
P97846	Contactin-associated protein 1	Cntnap1 Caspr Nrxn4	Rattus norvegicus (Norway rat)	17	4
Q9Y5G0	Protocadherin gamma-B5	PCDHGB5	Homo sapiens (human)	2	4
Q709C8	Intermembrane lipid transfer protein VPS13C	VPS13C KIAA1421	Homo sapiens (human)	2	4
P29788	Vitronectin	Vtn	Mus musculus (house mouse)	3	4
Q9BZ95	Histone-lysine N-methyltransferase NSD3	NSD3 WHSC1L1	Homo sapiens (human)	4	4
E9PVG8	Fc fragment of IgG binding protein like 1	Fcgbpl1 9530053A07Rik	Mus musculus (house mouse)	3	4

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements