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 **851 - 875** 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
O35764	Neuronal pentraxin receptor	Nptxr Npr	Rattus norvegicus (Norway rat)	3	15
Q8WWI5	Choline transporter-like protein 1	SLC44A1 CD92 CDW92 CTL1	Homo sapiens (human)	3	15
Q9Y287	Integral membrane protein 2B	ITM2B BRI BRI2	Homo sapiens (human)	1	15
Q8K135	Dyslexia-associated protein KIAA0319-like protein	Kiaa0319l Aavr	Mus musculus (house mouse)	9	15
O15394	Neural cell adhesion molecule 2	NCAM2 NCAM21	Homo sapiens (human)	11	15
P12346	Serotransferrin	Tf	Rattus norvegicus (Norway rat)	1	15
P08174	Complement decay-accelerating factor	CD55 CR DAF	Homo sapiens (human)	8	15	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 Barrett's esophagus Budd-Chiari syndrome IgA glomerulonephritis Kallmann syndrome Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Patau syndrome Pick's disease Plasmodium vivax malaria Reye syndrome Richter's syndrome Sheehan syndrome T-cell acute lymphoblastic leukemia Weissenbacher-Zweymuller syndrome Werner syndrome acoustic neuroma acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia adenocarcinoma adenoma adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome agammaglobulinemia age related macular degeneration amphetamine abuse amyloidosis anaplastic astrocytoma anemia angiomatous meningioma aplastic anemia arthritis arthropathy atopic dermatitis atrial fibrillation autoimmune disease autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome bacterial infectious disease benign meningioma beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma bullous pemphigoid cancer carcinoma central nervous system lymphoma cerebral convexity meningioma cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood lymphoma cholangiocarcinoma cholera chronic kidney disease chronic lymphocytic leukemia chronic myeloid leukemia chronic pyelonephritis clear cell meningioma colitis colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma 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 congenital hemolytic anemia cribriform carcinoma critical illness polyneuropathy deficiency anemia degeneration of macula and posterior pole dermatitis diabetes mellitus diabetic ketoacidosis diarrhea embryoma endometrial cancer endometrial carcinoma endometrial serous adenocarcinoma endometriosis of ovary endometriosis of uterus endometriosis esophagus adenocarcinoma essential thrombocythemia eunuchism familial adenomatous polyposis 1 familial adenomatous polyposis favism fetal erythroblastosis fibrillary astrocytoma fibrous meningioma follicular lymphoma gastroenteritis gastrointestinal stromal tumor gemistocytic astrocytoma granular cell carcinoma hemoglobinopathy hemolytic anemia hepatitis C hereditary elliptocytosis hereditary spherocytosis high grade glioma hypochromic anemia hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis ileus immune system disease inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease influenza intestinal obstruction intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma islet cell tumor isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency juvenile pilocytic astrocytoma kwashiorkor large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lymphoma macrocytic anemia macroglobulinemia macular degeneration malaria malignant astrocytoma marasmus meningioma meningoencephalitis meningothelial meningioma microcystic meningioma microcytic anemia myasthenia gravis myelodysplastic syndrome myositis neuroblastoma neuromyelitis optica neuropathy non-Hodgkin lymphoma nutrition disease obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma olfactory groove meningioma ovarian cancer ovarian carcinoma panhypopituitarism parasagittal meningioma paroxysmal nocturnal hemoglobinuria peripheral nervous system disease pilocytic astrocytoma pituitary adenoma pneumonia polyneuropathy progeria prostate cancer prostate carcinoma protein-energy malnutrition protein-losing enteropathy proteinuria protoplasmic astrocytoma psammomatous meningioma pulmonary embolism pure red-cell aplasia recurrent hypersomnia reticulosarcoma rheumatoid arthritis sarcoidosis sarcomatoid carcinoma secondary hypertrophic osteoarthropathy secretory meningioma septooptic dysplasia sickle cell anemia skin squamous cell carcinoma spinal meningioma stomach cancer stomach carcinoma subependymal giant cell astrocytoma systemic primary carnitine deficiency disease thalassemia thrombosis thrombotic thrombocytopenic purpura transitional meningioma tropical sprue tuberculosis tubular adenocarcinoma type 2 diabetes mellitus type I complement component 8 deficiency type II complement component 8 deficiency ulcerative colitis uterine corpus cancer
Q9UH99	SUN domain-containing protein 2	SUN2 FRIGG KIAA0668 RAB5IP UNC84B	Homo sapiens (human)	6	15
Q9UBS9	SUN domain-containing ossification factor	SUCO C1orf9 CH1 OPT SLP1	Homo sapiens (human)	14	15
Q9QY33	Tetraspanin-3	Tspan3 Tm4sf8	Mus musculus (house mouse)	4	15
Q922J6	Tetraspanin-2	Tspan2	Mus musculus (house mouse)	1	15
Q9QYS2	Metabotropic glutamate receptor 3	Grm3 Gprc1c Mglur3	Mus musculus (house mouse)	4	15
Q9UNW1	Multiple inositol polyphosphate phosphatase 1	MINPP1 MIPP	Homo sapiens (human)	7	15	actinic keratosis cancer carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colonic benign neoplasm colorectal cancer head and neck cancer large intestine cancer multiple myeloma nodular goiter papillary adenocarcinoma papillary renal cell carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma seborrheic keratosis skin disease spinal cord disease thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma
P13595	Neural cell adhesion molecule 1	Ncam1 Ncam	Mus musculus (house mouse)	23	15
P48307	Tissue factor pathway inhibitor 2	TFPI2	Homo sapiens (human)	2	15
O09126	Semaphorin-4D	Sema4d Semacl2 Semaj	Mus musculus (house mouse)	9	15
Q9UQP3	Tenascin-N	TNN TNW	Homo sapiens (human)	4	15
P05121	Plasminogen activator inhibitor 1	SERPINE1 PAI1 PLANH1	Homo sapiens (human)	6	15
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
Q9WTS6	Teneurin-3	Tenm3 Kiaa1455 Odz3 Tnm3	Mus musculus (house mouse)	19	14
Q61847	Meprin A subunit beta	Mep1b Mep-1b	Mus musculus (house mouse)	10	14
O35114	Lysosome membrane protein 2	Scarb2	Mus musculus (house mouse)	11	14
P60882	Multiple epidermal growth factor-like domains protein 8	Megf8 Egfl4	Mus musculus (house mouse)	18	14
Q80V42	Carboxypeptidase M	Cpm	Mus musculus (house mouse)	4	14

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