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 **18301 - 18325** 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
O00193	Small acidic protein	SMAP C11orf58	Homo sapiens (human)	2	1
B1GYE7	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q92575	UBX domain-containing protein 4	UBXN4 KIAA0242 UBXD2 UBXDC1	Homo sapiens (human)	1	2
Q99944	Epidermal growth factor-like protein 8	EGFL8 C6orf8 NG3	Homo sapiens (human)	1	0
A0A563ZYY7	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9UNZ5	Leydig cell tumor 10 kDa protein homolog	C19orf53	Homo sapiens (human)	0	1
Q9UL16	Cilia- and flagella-associated protein 45	CFAP45 CCDC19 NESG1	Homo sapiens (human)	0	1
Q7Z5P4	17-beta-hydroxysteroid dehydrogenase 13	HSD17B13 SCDR9 SDR16C3	Homo sapiens (human)	1	1
P27824	Calnexin	CANX	Homo sapiens (human)	11	5	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 Lyme disease MASA syndrome Marfan syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 absence epilepsy acute myocardial infarction adult medulloblastoma agenesis of the corpus callosum with peripheral neuropathy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bone osteosarcoma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system lymphoma cervical squamous cell carcinoma cervix uteri carcinoma in situ childhood absence epilepsy childhood medulloblastoma childhood osteosarcoma cone-rod dystrophy coronary artery disease coronary thrombosis diabetes mellitus diabetic angiopathy diabetic ketoacidosis embryoma exanthema subitum fundus albipunctatus giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 high grade glioma hyperinsulinism interstitial lung disease keratosis follicularis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lymphoma measles medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma mongolian spot monoclonal gammopathy of uncertain significance motor peripheral neuropathy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple myeloma multiple sclerosis myocardial infarction nephrogenic diabetes insipidus neuropathy nodular prostate obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum oculocutaneous albinism type IA oculocutaneous albinism osteosarcoma peripheral nervous system disease platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 polyneuropathy post-traumatic stress disorder progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma pseudoachondroplasia pseudoxanthoma elasticum renal tubular acidosis retinitis pigmentosa rubella silent myocardial infarction situs inversus skin melanoma spinal muscular atrophy stomach cancer stomach carcinoma tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus vitiligo von Willebrand's disease
Q13670	Putative postmeiotic segregation increased 2-like protein 11	PMS2P11 PMS2L11 PMSR6	Homo sapiens (human)	0	1
A0A7D9CT54	MHC Class I chain-related protein	MICA	Homo sapiens (human)	3	0
P23219	Prostaglandin G/H synthase 1	PTGS1 COX1	Homo sapiens (human)	3	6	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 Barrett's esophagus Creutzfeldt-Jakob disease Evans' syndrome French Canadian Leigh disease Guillain-Barre syndrome Hantavirus hemorrhagic fever with renal syndrome Leigh disease Lyme disease Marfan syndrome Meckel syndrome Miller Fisher syndrome Pick's disease Reye syndrome Streptococcus pneumonia acoustic neuroma acquired immunodeficiency syndrome actinic keratosis acute chest syndrome acute myeloid leukemia acute myocardial infarction acute promyelocytic leukemia adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma amnestic disorder amyloidosis angiomatous meningioma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma ataxia telangiectasia atherosclerosis autism spectrum disorder autistic disorder autoimmune polyendocrine syndrome autoimmune thrombocytopenic purpura autosomal dominant polycystic kidney disease basal cell carcinoma benign meningioma bipolar disorder bladder carcinoma blood coagulation disease brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma bursitis cancer carcinoma cardiac arrest cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral convexity meningioma cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia childhood type dermatomyositis chorioamnionitis chromophobe renal cell carcinoma chronic ethmoiditis chronic kidney disease chronic myeloid leukemia chronic obstructive pulmonary disease chronic sphenoidal sinusitis clear cell meningioma clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cytochrome-c oxidase deficiency disease depressive disorder dermatomyositis diabetes mellitus diabetic ketoacidosis dysthymic disorder eclampsia embryoma epilepsy erythromelalgia esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue eyelid disease familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia fibrous meningioma follicular adenoma frozen shoulder gastric lymphoma gastric ulcer gastritis gastroenteritis gastroesophageal reflux disease gastrointestinal system cancer gastrointestinal system disease giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hemiplegia hepatic coma hepatic encephalopathy hepatitis hepatocellular carcinoma high grade glioma histiocytosis human immunodeficiency virus infectious disease hyperglycemia hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome inflammatory bowel disease 1 inflammatory bowel disease influenza intestinal disease intracranial vasospasm intraorbital meningioma intraventricular meningioma intrinsic asthma islet cell tumor isovaleric acidemia keratoacanthoma kidney disease kidney failure lactic acidosis large intestine cancer leukemia liver cancer lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lupus erythematosus lupus nephritis lymphoplasmacyte-rich meningioma major depressive disorder meconium aspiration syndrome melancholic depression melanoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma mixed glioma mood disorder mucoepidermoid carcinoma multiple myeloma myocardial infarction myositis nephritis nephrosis neurogenic arthropathy neuromuscular disease neurotic disorder nonpapillary renal cell carcinoma nose disease nutmeg liver obesity obsolete dyspepsia obsolete inherited blood coagulation disease obsolete melancholia obstructive sleep apnea olfactory groove meningioma osteoarthritis ovarian cancer ovarian carcinoma ovarian cyst oxyphilic adenoma pancreatic cancer pancreatic carcinoma papillary adenoma papillary carcinoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma peptic esophagitis peptic ulcer disease peripheral artery disease pituitary adenoma platelet-type bleeding disorder 12 pneumonia pneumothorax portal hypertension pre-eclampsia primary immunodeficiency disease primary open angle glaucoma primary pulmonary hypertension prostate cancer prostate carcinoma psammomatous meningioma psoriasis psoriatic arthritis pustulosis of palm and sole pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma renovascular hypertension retrograde amnesia rheumatoid arthritis root resorption sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia secretory meningioma silent myocardial infarction situs inversus skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal meningioma spindle cell hemangioma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma synovitis systemic lupus erythematosus tenosynovitis thrombocytopenia due to platelet alloimmunization thrombocytopenia thrombosis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma tongue squamous cell carcinoma transient cerebral ischemia transitional meningioma tuberous sclerosis 1 tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uremia urinary bladder cancer urinary tract obstruction viral infectious disease visual epilepsy xanthomatosis
M9P990	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q13882	Protein-tyrosine kinase 6	PTK6 BRK	Homo sapiens (human)	0	1
U3RCP7	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
F2X5V9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q02763	Angiopoietin-1 receptor	TEK TIE2 VMCM VMCM1	Homo sapiens (human)	10	12
M9P8R6	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9NY72	Sodium channel regulatory subunit beta-3	SCN3B KIAA1158	Homo sapiens (human)	4	0
J3KPQ0	Fibroblast growth factor receptor	FGFR4	Homo sapiens (human)	1	0
A0A060VCZ5	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9NVI1	Fanconi anemia group I protein	FANCI KIAA1794	Homo sapiens (human)	0	1
Q13651	Interleukin-10 receptor subunit alpha	IL10RA IL10R	Homo sapiens (human)	6	0
Q9NVU0	DNA-directed RNA polymerase III subunit RPC5	POLR3E KIAA1452	Homo sapiens (human)	1	2
O14626	G-protein coupled receptor 171	GPR171 H963	Homo sapiens (human)	1	0

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