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 **1751 - 1775** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
P69891	Hemoglobin subunit gamma-1	HBG1	Homo sapiens (human)	1
P0CG48	Polyubiquitin-C	UBC	Homo sapiens (human)	1
Q8TCT0	Ceramide kinase	CERK KIAA1646	Homo sapiens (human)	1	Kaposi's sarcoma breast cancer breast carcinoma cancer colitis gastroenteritis ileitis ileocolitis microphthalmia neuroblastoma obesity obsolete Matthew-Wood syndrome schizophrenia 10 schizophrenia
Q5TBC7	Bcl-2-like protein 15	BCL2L15 C1orf178	Homo sapiens (human)	1
P36873	Serine/threonine-protein phosphatase PP1-gamma catalytic subunit	PPP1CC	Homo sapiens (human)	1
Q96S44	EKC/KEOPS complex subunit TP53RK	TP53RK C20orf64 PRPK	Homo sapiens (human)	1
Q15102	Platelet-activating factor acetylhydrolase IB subunit alpha1	PAFAH1B3 PAFAHG	Homo sapiens (human)	1	intellectual disability learning disability
P24941	Cyclin-dependent kinase 2	CDK2 CDKN2	Homo sapiens (human)	1
P55157	Microsomal triglyceride transfer protein large subunit	MTTP MTP	Homo sapiens (human)	1
A8MV65	Transcription cofactor vestigial-like protein 3	VGLL3	Homo sapiens (human)	1
O00232	26S proteasome non-ATPase regulatory subunit 12	PSMD12	Homo sapiens (human)	1
O75901	Ras association domain-containing protein 9	RASSF9 PAMCI PCIP1	Homo sapiens (human)	1
Q5T6V5	Queuosine 5'-phosphate N-glycosylase/hydrolase	QNG1 C9orf64	Homo sapiens (human)	1
P07741	Adenine phosphoribosyltransferase	APRT	Homo sapiens (human)	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
Q6ZWH5	Serine/threonine-protein kinase Nek10	NEK10	Homo sapiens (human)	1
Q8WUD4	Coiled-coil domain-containing protein 12	CCDC12	Homo sapiens (human)	1
Q7Z570	Zinc finger protein 804A	ZNF804A C2orf10	Homo sapiens (human)	1
Q96MP5	Zinc finger SWIM domain-containing protein 3	ZSWIM3 C20orf164	Homo sapiens (human)	1
Q96JN8	Neuralized-like protein 4	NEURL4 KIAA1787	Homo sapiens (human)	1
Q96S90	LysM and putative peptidoglycan-binding domain-containing protein 1	LYSMD1	Homo sapiens (human)	1
Q9ULJ6	Zinc finger MIZ domain-containing protein 1	ZMIZ1 KIAA1224 RAI17 ZIMP10	Homo sapiens (human)	1
O15116	U6 snRNA-associated Sm-like protein LSm1	LSM1 CASM	Homo sapiens (human)	1
P55084	Trifunctional enzyme subunit beta, mitochondrial	HADHB	Homo sapiens (human)	1	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 Norum disease Tangier disease X-linked dilated cardiomyopathy abetalipoproteinemia adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy agnosia beta-ketothiolase deficiency breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease cholestasis choreaacanthocytosis clubfoot colorectal cancer colorectal carcinoma cone-rod dystrophy congestive heart failure critical illness polyneuropathy developmental coordination disorder dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy embryoma endomyocardial fibrosis epilepsy familial hyperlipidemia familial periodic paralysis fibromyalgia fundus albipunctatus heart disease hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hypercalcemia hypertrophic cardiomyopathy hypolipoproteinemia hypoparathyroidism inflammatory and toxic neuropathy intellectual disability lactic acidosis large intestine cancer learning disability melanoma meningoencephalitis mitochondrial trifunctional protein deficiency mitral valve insufficiency mitral valve prolapse motor peripheral neuropathy myoglobinuria myopathy myositis nephrocalcinosis neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease phosphorus metabolism disease placental insufficiency polydactyly polyneuropathy prostate adenocarcinoma prostate cancer prostate carcinoma prostatitis pseudohypoparathyroidism pseudosarcomatous fibromatosis retinitis pigmentosa sick sinus syndrome skin melanoma steatotic liver disease tricuspid valve insufficiency urea cycle disorder visual epilepsy
Q49AR2	UPF0489 protein C5orf22	C5orf22	Homo sapiens (human)	1
Q9BUE0	Mediator of RNA polymerase II transcription subunit 18	MED18	Homo sapiens (human)	1

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