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 **17776 - 17800** 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
P06028	Glycophorin-B	GYPB GPB	Homo sapiens (human)	4	13
Q5T2D2	Trem-like transcript 2 protein	TREML2 C6orf76 TLT2	Homo sapiens (human)	1	13
O60566	Mitotic checkpoint serine/threonine-protein kinase BUB1 beta	BUB1B BUBR1 MAD3L SSK1	Homo sapiens (human)	4	13
Q06418	Tyrosine-protein kinase receptor TYRO3	TYRO3 BYK DTK RSE SKY TIF	Homo sapiens (human)	7	13
P05981	Serine protease hepsin	HPN TMPRSS1	Homo sapiens (human)	1	13
O00462	Beta-mannosidase	MANBA MANB1	Homo sapiens (human)	8	13	Fabry disease allergic asthma allergic disease alternating hemiplegia of childhood angiokeratoma ascending cholangitis asthma attention deficit hyperactivity disorder autonomic neuropathy beta-mannosidosis central nervous system disease cholangitis chronic kidney disease chylomicron retention disease colorectal cancer colorectal carcinoma complement deficiency congenital nystagmus dissociated nystagmus epilepsy intellectual disability intrinsic asthma large intestine cancer learning disability lipid storage disease lysosomal storage disease multiple sclerosis nervous system disease obsolete constipation pathologic nystagmus primary biliary cholangitis primary sclerosing cholangitis sarcoidosis sclerosing cholangitis sensorineural hearing loss speech disorder spontaneous ocular nystagmus suppurative cholangitis uveoparotid fever visual epilepsy
O94905	Erlin-2	ERLIN2 C8orf2 SPFH2	Homo sapiens (human)	7	13
Q16585	Beta-sarcoglycan	SGCB	Homo sapiens (human)	4	13
Q92791	Endoplasmic reticulum protein SC65	P3H4 LEPREL4 NOL55 SC65	Homo sapiens (human)	3	13
P27701	CD82 antigen	CD82 KAI1 SAR2 ST6 TSPAN27	Homo sapiens (human)	5	13
Q96RL7	Intermembrane lipid transfer protein VPS13A	VPS13A CHAC KIAA0986	Homo sapiens (human)	2	14
P04156	Major prion protein	PRNP ALTPRP PRIP PRP	Homo sapiens (human)	6	14	3p deletion syndrome Alpers-Huttenlocher syndrome 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 Angelman syndrome Balo concentric sclerosis Bernard-Soulier syndrome 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 Chediak-Higashi syndrome Cockayne syndrome Cornelia de Lange syndrome Creutzfeldt-Jakob disease Down syndrome Dubowitz syndrome Friedreich ataxia Gerstmann-Straussler-Scheinker syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease ITM2B-related cerebral amyloid angiopathy 1 Japanese encephalitis Kennedy's disease Lewy body dementia MYH-9 related disease Marfan syndrome NFIA-related disorder 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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pelger-Huet anomaly Pick's disease Prader-Willi syndrome REM sleep behavior disorder Reye syndrome Robinow syndrome SATB2-associated syndrome Seckel syndrome Silver-Russell syndrome Smith-Magenis syndrome Unverricht-Lundborg syndrome Wilson disease X-linked Aarskog syndrome acoustic neuroma acquired immunodeficiency syndrome acute myocardial infarction adenocarcinoma adenoma adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy agnosia akinetic mutism alcoholic hepatitis allergic asthma alopecia alternating hemiplegia of childhood amnestic disorder amyloidosis amyotrophic lateral sclerosis anaplastic astrocytoma androgenic alopecia anxiety disorder aphasia apraxia arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis attention deficit hyperactivity disorder autonomic neuropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cerebellar ataxia autosomal recessive Robinow syndrome bipolar disorder blepharospasm blindness bone osteosarcoma brain disease brain ischemia brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cellular schwannoma central nervous system cancer central nervous system disease cerebellar ataxia cerebellar disease cerebral amyloid angiopathy cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood cerebral astrocytoma childhood osteosarcoma chondrodysplasia-pseudohermaphroditism syndrome chondrosarcoma choreatic disease chromophobe renal cell carcinoma chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome chronic kidney disease chronic obstructive pulmonary disease chronic wasting disease clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma common wart complex partial epilepsy cone-rod dystrophy congenital diarrhea 5 with tufting enteropathy congenital nystagmus conversion disorder coronary artery disease coronary thrombosis cribriform carcinoma critical illness polyneuropathy cystic fibrosis dementia demyelinating polyneuropathy dengue disease dentatorubral-pallidoluysian atrophy depressive disorder diabetic cataract diabetic retinopathy diarrhea dissociated nystagmus dissociative disorder distal 10q deletion syndrome dysthymic disorder early myoclonic encephalopathy embryoma encephalitis encephalomyelitis epilepsy essential hypertension factor VIII deficiency familial mediterranean fever familial periodic paralysis fatal familial insomnia fibrillary astrocytoma focal hand dystonia frontotemporal dementia frozen shoulder fundus albipunctatus gemistocytic astrocytoma generalized anxiety disorder giant cell glioblastoma glaucoma glioblastoma gliosarcoma granular cell carcinoma head and neck squamous cell carcinoma hemochromatosis hepatitis B hepatitis C hepatocellular carcinoma hereditary ataxia hereditary neuropathy with liability to pressure palsies high grade glioma human immunodeficiency virus infectious disease hydrocephalus hyperekplexia 1 hyperekplexia 2 hyperekplexia 3 hyperekplexia hyperglycemia hypertension hypothalamic disease inclusion body myositis inflammatory and toxic neuropathy inflammatory bowel disease influenza intrinsic asthma iron metabolism disease juvenile pilocytic astrocytoma juvenile rheumatoid arthritis kuru large intestine cancer lingual-facial-buccal dyskinesia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder malignant astrocytoma malignant peripheral nerve sheath tumor melancholic depression melanoma melanotic neurilemmoma meningitis meningoencephalitis mevalonic aciduria microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microphthalmia migraine mixed glioma mood disorder motor peripheral neuropathy movement disease multiple sclerosis multiple system atrophy myelitis myocardial infarction myopathy myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 narcolepsy neovascular glaucoma nervous system disease neurilemmoma neuroblastoma neurodegenerative disease neuropathy neurotic disorder normal pressure hydrocephalus obesity obsolete Alpers syndrome obsolete Matthew-Wood syndrome obsolete constipation obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia ocular hypotension osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma parathyroid gland disease paroxysmal nocturnal hemoglobinuria pathologic nystagmus peripheral nervous system disease pilocytic astrocytoma pityriasis rubra pilaris placental insufficiency plexiform schwannoma polyneuropathy primary cerebellar degeneration primary cutaneous amyloidosis primary open angle glaucoma prion disease progressive multifocal leukoencephalopathy progressive muscular atrophy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy 4 progressive myoclonus epilepsy progressive supranuclear palsy prostate cancer prostate carcinoma protoplasmic astrocytoma psychotic disorder qualitative platelet defect radial nerve lesion radial neuropathy recurrent hypersomnia renal carcinoma renal cell carcinoma retinitis pigmentosa retrograde amnesia sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder scrapie secondary Parkinson disease sickle cell anemia silent myocardial infarction situs inversus skin melanoma spinal muscular atrophy spinocerebellar ataxia type 31 spinocerebellar ataxia type 7 spontaneous ocular nystagmus squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma sudden infant death syndrome syndromic X-linked intellectual disability type 10 synovitis tauopathy temporal lobe epilepsy tendinitis tenosynovitis tongue squamous cell carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trigeminal neuralgia tuberous sclerosis tubular adenocarcinoma vascular dementia vestibular nystagmus viral infectious disease visual epilepsy vitiligo yellow fever
P13497	Bone morphogenetic protein 1	BMP1 PCOLC	Homo sapiens (human)	7	14
Q9BZC7	ATP-binding cassette sub-family A member 2	ABCA2 ABC2 KIAA1062	Homo sapiens (human)	27	14
P41271	Neuroblastoma suppressor of tumorigenicity 1	NBL1 DAN DAND1	Homo sapiens (human)	3	14
O94923	D-glucuronyl C5-epimerase	GLCE KIAA0836	Homo sapiens (human)	8	14	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions amyotrophic lateral sclerosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer embryoma essential hypertension frontotemporal dementia hypertension luminal breast carcinoma A lung benign neoplasm lung cancer lung carcinoma lung small cell carcinoma nodular prostate progressive muscular atrophy prostate cancer prostate carcinoma prostate disease prostatic adenoma
O75094	Slit homolog 3 protein	SLIT3 KIAA0814 MEGF5 SLIL2	Homo sapiens (human)	16	14
P08246	Neutrophil elastase	ELANE ELA2	Homo sapiens (human)	4	14
Q9UNN8	Endothelial protein C receptor	PROCR EPCR	Homo sapiens (human)	4	14
Q9C0C4	Semaphorin-4C	SEMA4C KIAA1739 SEMAI	Homo sapiens (human)	7	14
P56159	GDNF family receptor alpha-1	GFRA1 GDNFRA RETL1 TRNR1	Homo sapiens (human)	6	14	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 Hirschsprung's disease Kennedy's disease Pick's disease Reye syndrome acute promyelocytic leukemia adult cystic teratoma adult teratoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease autosomal recessive distal hereditary motor neuronopathy 1 bone osteosarcoma brain cancer brain ischemia breast cancer breast carcinoma breast fibrocystic disease cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma colorectal cancer colorectal carcinoma cystic teratoma embryoma embryonal cancer endemic goiter germ cell and embryonal cancer germ cell cancer hepatitis C hepatocellular carcinoma idiopathic scoliosis large intestine cancer lateral sclerosis lesion of sciatic nerve liver cancer malignant teratoma mature teratoma melanoma microglandular adenosis migraine without aura motor neuron disease neuroendocrine carcinoma neuroendocrine tumor neuropathy obsolete ymphosarcoma osteosarcoma pancreatic cancer pancreatic carcinoma peripheral nervous system disease polyneuropathy preretinal fibrosis progressive muscular atrophy prostate cancer prostate carcinoma rheumatoid arthritis schizophrenia sciatic neuropathy secondary Parkinson disease skin melanoma substernal goiter teratoma thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma vascular dementia vesicoureteral reflux
Q02383	Semenogelin-2	SEMG2	Homo sapiens (human)	2	14
O76024	Wolframin	WFS1	Homo sapiens (human)	2	14
O15460	Prolyl 4-hydroxylase subunit alpha-2	P4HA2	Homo sapiens (human)	5	14
O75636	Ficolin-3	FCN3 FCNH HAKA1	Homo sapiens (human)	1	14	Crohn's colitis Crohn's disease abdominal aortic aneurysm acute myocardial infarction amyotrophic lateral sclerosis anogenital venereal wart arteriosclerotic cardiovascular disease atherosclerosis bacterial infectious disease cancer common wart complement component 2 deficiency complement component 4a deficiency complement component 4b deficiency complement component 6 deficiency complement component 7 deficiency complement component 9 deficiency complement deficiency coronary artery disease coronary thrombosis diabetes mellitus essential hypertension gestational diabetes hepatocellular carcinoma hypertension inflammatory bowel disease 1 inflammatory bowel disease interstitial lung disease leprosy liver cancer lupus nephritis myocardial infarction ovarian cancer ovarian carcinoma placental insufficiency primary immunodeficiency disease progressive muscular atrophy sarcoidosis scleroderma silent myocardial infarction systemic lupus erythematosus systemic scleroderma tuberculosis type 2 diabetes mellitus type I complement component 8 deficiency type II complement component 8 deficiency ulcerative colitis

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