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 **13926 - 13950** 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
Q9NWX6	Probable tRNA(His) guanylyltransferase	THG1L ICF45	Homo sapiens (human)	1	1
A0A2R8VHF9	Myosin-11	Myh11	Mus musculus (house mouse)	0	1
A0A1P8B895	K-box region and MADS-box transcription factor family protein	STK AGAMOUS-like 11 AGL11 SEEDSTICK	Arabidopsis thaliana (thale cress)	0	1
O42486	Catenin beta-1	Bcat	Gallus gallus (chicken)	4	1
Q62010	Oviduct-specific glycoprotein	Ovgp1 Chit5 Ogp	Mus musculus (house mouse)	4	1
Q8JZK6	RING finger protein 35	Trim61 Rnf35	Mus musculus (house mouse)	2	1
Q8K1A6	Coiled-coil and C2 domain-containing protein 1A	Cc2d1a	Mus musculus (house mouse)	0	1
Q9UPN7	Serine/threonine-protein phosphatase 6 regulatory subunit 1	PPP6R1 KIAA1115 PP6R1 SAPS1	Homo sapiens (human)	3	1
O00232	26S proteasome non-ATPase regulatory subunit 12	PSMD12	Homo sapiens (human)	0	1
O75901	Ras association domain-containing protein 9	RASSF9 PAMCI PCIP1	Homo sapiens (human)	0	1
O43541	Mothers against decapentaplegic homolog 6	SMAD6 MADH6	Homo sapiens (human)	2	1
Q5T6V5	Queuosine 5'-phosphate N-glycosylase/hydrolase	QNG1 C9orf64	Homo sapiens (human)	0	1
P07741	Adenine phosphoribosyltransferase	APRT	Homo sapiens (human)	0	1	Albright's hereditary osteodystrophy 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 Becker muscular dystrophy Bloom syndrome Brucella melitensis brucellosis Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome Carney complex Danon disease Duchenne muscular dystrophy Gerstmann-Straussler-Scheinker syndrome Gorham's disease Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Langerhans-cell histiocytosis Lesch-Nyhan syndrome Lown-Ganong-Levine syndrome Marfan syndrome McCune Albright syndrome Meckel syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Peutz-Jeghers syndrome Pick's disease Q fever Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia Werdnig-Hoffmann disease Werner syndrome Wolff-Parkinson-White syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acquired hyperkeratosis acrodermatitis acrodysostosis acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction acute promyelocytic leukemia adenine phosphoribosyltransferase deficiency adenocarcinoma adenoma adenosarcoma adrenal gland cancer adrenal gland hyperfunction adrenoleukodystrophy adult T-cell leukemia/lymphoma adult acute lymphocytic leukemia adult fibrosarcoma adult hepatocellular carcinoma adult medulloblastoma alcohol dependence alcohol use disorder allergic asthma amyloidosis amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anaplastic astrocytoma anterior horn cell disease arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atrichia with papular lesions atrioventricular block attention deficit hyperactivity disorder autistic disorder autoimmune polyendocrine syndrome autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal dominant polycystic kidney disease autosomal recessive distal hereditary motor neuronopathy 1 autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bacterial infectious disease bacterial sepsis benign mesothelioma bile duct adenocarcinoma bile duct cancer bile duct carcinoma bladder carcinoma bone osteosarcoma brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ cherubism childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood hepatocellular carcinoma childhood leukemia childhood medulloblastoma childhood optic nerve glioma childhood osteosarcoma childhood spinal muscular atrophy cholangiocarcinoma cholera chondrosarcoma choriocarcinoma chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation congenital muscular dystrophy congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cystic fibrosis cystinosis cystinuria dengue disease depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diarrhea diffuse large B-cell lymphoma disease of metabolism distal arthrogryposis distal myopathy duodenum cancer dysentery dysthymic disorder embryoma encephalitis encephalomyelitis endocarditis endocrine exophthalmos endometrial cancer endometrial carcinoma endomyocardial fibrosis epilepsy episodic kinesigenic dyskinesia 1 esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension exostosis facioscapulohumeral muscular dystrophy familial hyperlipidemia familial hypertrophic cardiomyopathy familial retinoblastoma fibrillary astrocytoma fibrodysplasia ossificans progressiva fibrolamellar carcinoma fibromyalgia fibrosarcoma fibrous dysplasia follicular adenoma fragile X syndrome galactosemia gallbladder cancer gallbladder carcinoma gemistocytic astrocytoma giant cell glioblastoma glaucoma glioblastoma gliosarcoma glomerulonephritis glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease V glycogen storage disease VI glycogen storage disease VII glycogen storage disease glycoproteinosis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart cancer heart disease hepatitis B hepatitis C hepatitis hepatoblastoma hepatocellular carcinoma hereditary breast ovarian cancer syndrome high grade glioma hyperglycemia hypertension hyperthyroidism hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy hypoglycemia hypoparathyroidism hypothalamic disease idiopathic interstitial pneumonia immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome impulse control disorder influenza intermittent explosive disorder interstitial nephritis intestinal infectious disease intrahepatic cholangiocarcinoma intrinsic asthma irritant dermatitis juvenile pilocytic astrocytoma juvenile spinal muscular atrophy keratosis follicularis kidney cancer kidney disease kidney failure kleptomania large intestine cancer lateral sclerosis leishmaniasis leukemia leukoencephalopathy with vanishing white matter limb-girdle muscular dystrophy lipoatrophic diabetes mellitus lipodystrophy liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder malignant astrocytoma malignant mesothelioma malignant pleural mesothelioma maturity-onset diabetes of the young measles medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningitis methemoglobinemia microcystic adenoma microphthalmia mitochondrial metabolism disease mitochondrial myopathy mixed glioma mongolian spot motor neuron disease mucolipidosis II alpha/beta mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis VI mucopolysaccharidosis multiple acyl-CoA dehydrogenase deficiency multiple endocrine neoplasia type 1 multiple myeloma multiple sclerosis muscular dystrophy myasthenia gravis myelitis myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myositis ossificans myositis nasopharynx carcinoma nephritis nephroblastoma nephrolithiasis nephrosis neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neurofibromatosis 1 neurofibromatosis neuromuscular disease neuropathy neurotic disorder non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver obesity obsolete Cushing's syndrome obsolete Matthew-Wood syndrome obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oculopharyngeal muscular dystrophy optic nerve glioma osteoarthritis osteoblastoma osteomalacia osteosarcoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma parapsoriasis parathyroid gland disease periodontitis peripheral nervous system disease pheochromocytoma pilocytic astrocytoma placenta cancer pneumonia polycystic kidney disease 1 polycystic ovary syndrome polyneuropathy postinflammatory pulmonary fibrosis prediabetes syndrome primary hyperaldosteronism primary hyperoxaluria primary hyperparathyroidism primary immunodeficiency disease primary pigmented nodular adrenocortical disease primary pulmonary hypertension progeria progressive muscular atrophy prostate adenocarcinoma prostate cancer prostate carcinoma protoplasmic astrocytoma pseudohypoparathyroidism pseudopseudohypoparathyroidism pseudoxanthoma elasticum psoriasis psoriatic arthritis pulmonary fibrosis purine-pyrimidine metabolic disorder pustulosis of palm and sole pyelitis pyelonephritis pyoureter radiculopathy renal carcinoma renal cell carcinoma reticulosarcoma retinoblastoma rheumatoid arthritis rickets rippling muscle disease 2 sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia sick sinus syndrome silent myocardial infarction situs inversus skin melanoma skin squamous cell carcinoma small intestine cancer steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma sulfhemoglobinemia systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma thyrotoxicosis trilateral retinoblastoma trypanosomiasis tuberculosis tuberous sclerosis 1 tuberous sclerosis tubular adenocarcinoma 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 typhus uremia uric acid nephrolithiasis urinary bladder cancer urinary tract obstruction uterine corpus cancer viral infectious disease visceral leishmaniasis von Hippel-Lindau disease yellow fever
Q8VCC9	Spondin-1	Spon1	Mus musculus (house mouse)	2	1
D3YWS3	Profilin	Pfn2	Mus musculus (house mouse)	0	1
Q6ZWH5	Serine/threonine-protein kinase Nek10	NEK10	Homo sapiens (human)	0	1
P54577	Tyrosine--tRNA ligase, cytoplasmic	YARS1 YARS	Homo sapiens (human)	3	1
Q9NQL9	Doublesex- and mab-3-related transcription factor 3	DMRT3 DMRTA3	Homo sapiens (human)	1	1
Q9Z331	Keratin, type II cytoskeletal 6B	Krt6b K6-beta Krt2-6b	Mus musculus (house mouse)	0	1
Q96EQ0	Small glutamine-rich tetratricopeptide repeat-containing protein beta	SGTB SGT2	Homo sapiens (human)	5	1
Q9EQU5	Protein SET	Set	Mus musculus (house mouse)	0	1
Q7Z422	SUZ RNA-binding domain-containing	SZRD1 C1orf144	Homo sapiens (human)	3	1
Q99NG0	Helicase ARIP4	Rad54l2 Arip4 Srisnf2l	Mus musculus (house mouse)	5	1
Q9CQI7	U2 small nuclear ribonucleoprotein B''	Snrpb2	Mus musculus (house mouse)	0	1
Q8WUD4	Coiled-coil domain-containing protein 12	CCDC12	Homo sapiens (human)	0	1

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