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 **501 - 525** 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
O75437	Zinc finger protein 254	ZNF254 BMZF5 ZNF539 ZNF91L	Homo sapiens (human)	0	1
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
Q9BUI4	DNA-directed RNA polymerase III subunit RPC3	POLR3C	Homo sapiens (human)	0	1
Q07912	Activated CDC42 kinase 1	TNK2 ACK1	Homo sapiens (human)	5	1
O95006	Olfactory receptor 2F2	OR2F2	Homo sapiens (human)	1	0
Q9NPC2	Potassium channel subfamily K member 9	KCNK9 TASK3	Homo sapiens (human)	1	0
C0KLR5	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
P22234	Bifunctional phosphoribosylaminoimidazole carboxylase/phosphoribosylaminoimidazole succinocarboxamide synthetase	PAICS ADE2 AIRC PAIS	Homo sapiens (human)	0	1
Q3ZCQ8	Mitochondrial import inner membrane translocase subunit TIM50	TIMM50 TIM50	Homo sapiens (human)	0	1
Q8ND71	GTPase IMAP family member 8	GIMAP8 IAN9 IANT	Homo sapiens (human)	0	1
Q8NBP7	Proprotein convertase subtilisin/kexin type 9	PCSK9 NARC1	Homo sapiens (human)	1	1
Q5H8A4	GPI ethanolamine phosphate transferase 2	PIGG GPI7	Homo sapiens (human)	1	0	cerebral degeneration epilepsy intellectual disability learning disability placental insufficiency visual epilepsy
Q9C0E2	Exportin-4	XPO4 KIAA1721	Homo sapiens (human)	2	3
Q9Y616	Interleukin-1 receptor-associated kinase 3	IRAK3	Homo sapiens (human)	2	2
O75564	Jerky protein homolog	JRK JH8	Homo sapiens (human)	1	1
Q9UHX3	Adhesion G protein-coupled receptor E2	ADGRE2 EMR2	Homo sapiens (human)	14	21
Q5RI15	Cytochrome c oxidase assembly protein COX20, mitochondrial	COX20 FAM36A	Homo sapiens (human)	0	1
O15431	High affinity copper uptake protein 1	SLC31A1 COPT1 CTR1	Homo sapiens (human)	2	0
Q8NBW4	Neutral amino acid transporter 9	SLC38A9 URLC11	Homo sapiens (human)	4	0
A0A583ZBG3	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9BQ67	Glutamate-rich WD repeat-containing protein 1	GRWD1 GRWD KIAA1942 WDR28	Homo sapiens (human)	0	1
Q2I2T0	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9BZR6	Reticulon-4 receptor	RTN4R NOGOR	Homo sapiens (human)	7	5	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 Balo concentric sclerosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome X-linked ichthyosis acute myeloid leukemia adrenoleukodystrophy adult lymphoma amyotrophic lateral sclerosis type 1 anaplastic astrocytoma autism spectrum disorder autistic disorder brain cancer brain disease brain stem infarction cancer central nervous system cancer central nervous system disease central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood cerebral astrocytoma childhood leukemia childhood lymphoma chronic fatigue syndrome ciliary body disease colorectal cancer colorectal carcinoma diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy embryoma encephalitis encephalomyelitis essential tremor fibrillary astrocytoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance hepatocellular carcinoma high grade glioma iris disease juvenile pilocytic astrocytoma large intestine cancer leukemia liver cancer liver carcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma lung small cell carcinoma lymphoma malignant astrocytoma malignant pleural mesothelioma melanoma mixed glioma multiple sclerosis myelitis narcolepsy nasopharynx carcinoma nervous system disease neuroblastoma obsolete ymphosarcoma optic neuritis panuveitis pilocytic astrocytoma prediabetes syndrome protoplasmic astrocytoma psychotic disorder relapsing-remitting multiple sclerosis schizoaffective disorder schizophrenia schizophreniform disorder skin melanoma squamous cell carcinoma subependymal giant cell astrocytoma teratocarcinoma tongue squamous cell carcinoma uveitis
D7NNV9	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A0A3S6RG33	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0

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