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 **15151 - 15175** 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
O75150	E3 ubiquitin-protein ligase BRE1B	RNF40 BRE1B KIAA0661	Homo sapiens (human)	1	1
Q5VTR2	E3 ubiquitin-protein ligase BRE1A	RNF20 BRE1A	Homo sapiens (human)	2	1
Q6ZNA4	E3 ubiquitin-protein ligase Arkadia	RNF111	Homo sapiens (human)	0	1
O95376	E3 ubiquitin-protein ligase ARIH2	ARIH2 ARI2 TRIAD1	Homo sapiens (human)	0	1
Q9Y4X5	E3 ubiquitin-protein ligase ARIH1	ARIH1 ARI MOP6 UBCH7BP	Homo sapiens (human)	0	1
Q6P9F5	E3 ubiquitin ligase TRIM40	TRIM40 RNF35	Homo sapiens (human)	1	2
O43734	E3 ubiquitin ligase TRAF3IP2	TRAF3IP2 C6orf2 C6orf4 C6orf5 C6orf6	Homo sapiens (human)	1	6
O94874	E3 UFM1-protein ligase 1	UFL1 KIAA0776 MAXER NLBP RCAD	Homo sapiens (human)	0	1
Q9Y4E5	E3 SUMO-protein ligase ZNF451	ZNF451 COASTER KIAA0576 KIAA1702	Homo sapiens (human)	0	1
P49792	E3 SUMO-protein ligase RanBP2	RANBP2 NUP358	Homo sapiens (human)	68	6
O75928	E3 SUMO-protein ligase PIAS2	PIAS2 PIASX	Homo sapiens (human)	1	2
O75925	E3 SUMO-protein ligase PIAS1	PIAS1 DDXBP1	Homo sapiens (human)	1	2
Q96MF7	E3 SUMO-protein ligase NSE2	NSMCE2 C8orf36 MMS21	Homo sapiens (human)	0	1
Q9HCI6	E3 SUMO-protein ligase KIAA1586	KIAA1586	Homo sapiens (human)	0	1
P11161	E3 SUMO-protein ligase EGR2	EGR2 KROX20	Homo sapiens (human)	14	3
Q9UII4	E3 ISG15--protein ligase HERC5	HERC5 CEB1 CEBP1	Homo sapiens (human)	1	1
Q96L91	E1A-binding protein p400	EP400 CAGH32 KIAA1498 KIAA1818 TNRC12	Homo sapiens (human)	57	4
P16581	E-selectin	SELE ELAM1	Homo sapiens (human)	11	0	Alzheimer's disease B-cell lymphoma Behcet's disease Clostridium difficile colitis Evans' syndrome Fabry disease Graves' disease IgA glomerulonephritis Japanese encephalitis Kaposi's sarcoma Kawasaki disease Kyasanur forest disease Langerhans-cell histiocytosis Meckel syndrome Mycoplasma pneumoniae pneumonia Plasmodium falciparum malaria Proteus syndrome Sjogren's syndrome T-cell acute lymphoblastic leukemia abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute biphenotypic leukemia acute chest syndrome acute leukemia acute lymphoblastic leukemia acute myocardial infarction acute pancreatitis adult acute lymphocytic leukemia adult lymphoma age related macular degeneration aggressive periodontitis alcoholic liver cirrhosis allergic asthma allergic contact dermatitis angioedema anthracosilicosis anthracosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis asthma atherosclerosis atopic dermatitis atrial fibrillation autoimmune polyendocrine syndrome autoimmune thrombocytopenic purpura autosomal dominant polycystic kidney disease biliary atresia brain ischemia brain stem infarction breast cancer breast carcinoma breast ductal carcinoma bronchiolitis obliterans bronchus cancer bronchus carcinoma brucellosis bullous pemphigoid cancer capillary disease carcinoma cardiac arrest cardiovascular system disease carotid artery disease celiac disease central nervous system lymphoma cerebral artery occlusion cerebral infarction cerebral malaria cerebrovascular disease cervical squamous cell carcinoma chancroid childhood acute lymphocytic leukemia childhood leukemia chromophobe renal cell carcinoma chronic ethmoiditis chronic fatigue syndrome chronic interstitial cystitis chronic kidney disease chronic sphenoidal sinusitis chylomicron retention disease clear cell renal cell carcinoma collagen disease collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart complement deficiency congestive heart failure connective tissue disease coronary artery disease coronary thrombosis degeneration of macula and posterior pole dengue disease dengue hemorrhagic fever depressive disorder dermatitis diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy duodenal ulcer embryoma encephalitis encephalomyelitis endocrine exophthalmos endometriosis of uterus endometriosis episodic kinesigenic dyskinesia 1 essential hypertension essential thrombocythemia familial hypercholesterolemia gastritis generalized atherosclerosis gingivitis glaucoma glomerulonephritis heart disease hemochromatosis type 1 hemochromatosis hepatitis B hepatocellular carcinoma hereditary hemorrhagic telangiectasia human immunodeficiency virus infectious disease hyperglycemia hypertension hyperthyroidism idiopathic interstitial pneumonia immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome inflammatory bowel disease 1 inflammatory bowel disease inflammatory breast carcinoma interstitial cystitis intracranial aneurysm intrinsic asthma invasive ductal carcinoma keratoconjunctivitis sicca keratosis follicularis kidney disease kidney failure large intestine cancer lepromatous leprosy leptospirosis leukemia leukopenia lipid storage disease liver cancer localized scleroderma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphogranuloma venereum lymphoma macular degeneration major depressive disorder malaria melancholic depression melanoma migraine mongolian spot multiple myeloma multiple sclerosis myelitis myocardial infarction myotonic dystrophy type 1 myotonic dystrophy type 2 necrotizing ulcerative gingivitis nephritis nephrosis neuroblastoma non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteoarthritis pancreatic cancer pancreatic carcinoma pancreatitis papillary adenocarcinoma papillary renal cell carcinoma parapsoriasis perinatal necrotizing enterocolitis periodontitis periodontosis postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma prune belly syndrome pseudoxanthoma elasticum psoriasis pulmonary embolism pulmonary fibrosis pulmonary tuberculosis pustulosis of palm and sole pyoureter renal carcinoma renal cell carcinoma reticulosarcoma retinal disease retinitis rheumatoid arthritis sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma scleroderma sickle cell anemia silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma synovial sarcoma systemic lupus erythematosus systemic scleroderma telangiectasis temporal arteritis thromboangiitis obliterans thrombophilia thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma tuberculous pneumothorax 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 ulcerative colitis urticaria uveoparotid fever varicose veins vascular disease viral infectious disease yaws yellow fever
Q13474	Dystrophin-related protein 2	DRP2	Homo sapiens (human)	4	1
P11532	Dystrophin	DMD	Homo sapiens (human)	6	3	Duchenne muscular dystrophy
Q09019	Dystrophia myotonica WD repeat-containing protein	DMWD DM9	Homo sapiens (human)	0	1
Q14118	Dystroglycan 1	DAG1	Homo sapiens (human)	59	22	Alzheimer's disease Becker muscular dystrophy Bethlem myopathy Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease Dandy-Walker syndrome Dubowitz syndrome Duchenne muscular dystrophy Ebola hemorrhagic fever Fukuyama congenital muscular dystrophy Joubert syndrome Lassa fever Lyme disease Marfan syndrome Miller-Dieker lissencephaly syndrome 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 Peters anomaly Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Walker-Warburg syndrome X-linked Aarskog syndrome X-linked dilated cardiomyopathy abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult medulloblastoma agnosia allergic asthma ameloblastoma ankylosing spondylitis anterior horn cell disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 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 recessive Robinow syndrome 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 brain cancer breast cancer breast carcinoma buphthalmos campomelic dysplasia cancer carcinoma cardiomyopathy cataract celiac disease central nervous system cancer childhood leukemia childhood medulloblastoma childhood type dermatomyositis chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coloboma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer common variable immunodeficiency communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A9 congenital muscular dystrophy congestive heart failure cornea plana coronary artery disease coronary thrombosis cortical dysplasia-focal epilepsy syndrome craniometaphyseal dysplasia cribriform carcinoma cryptorchidism dental caries dentin caries depressive disorder dermatomyositis developmental coordination disorder diabetes mellitus dilated cardiomyopathy 1A 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 distal myopathy embryoma endometrial cancer endometrial carcinoma endomyocardial fibrosis epilepsy esophageal cancer esophageal carcinoma essential hypertension facioscapulohumeral muscular dystrophy familial periodic paralysis focal epilepsy fundus dystrophy giant cell glioblastoma glaucoma glioblastoma gliosarcoma granular cell carcinoma heart septal defect high grade glioma hydranencephaly hydrocephalus hydrophthalmos hypertension hypertrophic cardiomyopathy immune system disease inclusion body myositis inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intrinsic asthma isolated elevated serum creatine phosphokinase levels juvenile rheumatoid arthritis large intestine cancer learning disability leukemia leukodystrophy limb-girdle muscular dystrophy lissencephaly lymphocytic choriomeningitis major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly microphthalmia mixed glioma muscular atrophy muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia myositis myotonic dystrophy type 1 myotonic dystrophy type 2 neurodegenerative disease neuromuscular disease neuropathy nonpapillary renal cell carcinoma obesity 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma parapsoriasis partial motor epilepsy peripheral nervous system disease polyneuropathy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 primary biliary cholangitis prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole recurrent corneal erosion renal carcinoma renal cell carcinoma retinal detachment rhabdomyosarcoma rippling muscle disease 2 sarcomatoid carcinoma sarcomatoid renal cell carcinoma senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly silent myocardial infarction situs inversus squamous cell carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type systemic lupus erythematosus tongue cancer tongue squamous cell carcinoma tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uterine corpus cancer visual epilepsy
Q9Y4J8	Dystrobrevin alpha	DTNA DRP3	Homo sapiens (human)	1	3
Q03001	Dystonin	DST BP230 BP240 BPAG1 DMH DT KIAA0728	Homo sapiens (human)	14	2
Q8IZA0	Dyslexia-associated protein KIAA0319-like protein	KIAA0319L AAVR KIAA1837	Homo sapiens (human)	27	32

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