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 **17001 - 17025** 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
P02655	Apolipoprotein C-II	APOC2 APC2	Homo sapiens (human)	4	4
Q70JA7	Chondroitin sulfate synthase 3	CHSY3 CHSY2 CSS3	Homo sapiens (human)	8	4	breast cancer central nervous system cancer colorectal cancer colorectal carcinoma gliosarcoma high grade glioma large intestine cancer mixed glioma pancreatic cancer pancreatic carcinoma
P16455	Methylated-DNA--protein-cysteine methyltransferase	MGMT	Homo sapiens (human)	4	4
Q9UKY1	Zinc fingers and homeoboxes protein 1	ZHX1	Homo sapiens (human)	15	4
Q8TDD5	Mucolipin-3	MCOLN3	Homo sapiens (human)	4	4
Q10469	Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	MGAT2	Homo sapiens (human)	8	4	Laron syndrome achondroplasia antithrombin III deficiency autosomal recessive chronic granulomatous disease 3 cancer chronic granulomatous disease clubfoot congenital disorder of glycosylation type II congenital disorder of glycosylation type IIa congenital disorder of glycosylation congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia craniosynostosis diabetes mellitus diabetic ketoacidosis disease of metabolism epilepsy factor XII deficiency gestational diabetes gingival hypertrophy gingival overgrowth microcephaly neuroblastoma obesity protein C deficiency protein S deficiency sensorineural hearing loss stereotypic movement disorder syndromic X-linked intellectual disability 94 thrombophilia type 2 diabetes mellitus ventricular septal defect visual epilepsy
Q96DB9	FXYD domain-containing ion transport regulator 5	FXYD5 DYSAD IWU1	Homo sapiens (human)	15	4
Q8N608	Inactive dipeptidyl peptidase 10	DPP10 DPRP3 KIAA1492	Homo sapiens (human)	7	4
Q14332	Frizzled-2	FZD2	Homo sapiens (human)	8	4
Q12789	General transcription factor 3C polypeptide 1	GTF3C1	Homo sapiens (human)	8	4
P54646	5'-AMP-activated protein kinase catalytic subunit alpha-2	PRKAA2 AMPK AMPK2	Homo sapiens (human)	1	4	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 Chediak-Higashi syndrome Clouston syndrome Duchenne muscular dystrophy Fanconi anemia complementation group A Fanconi anemia Friedreich ataxia 1 Friedreich ataxia Gilbert syndrome Graves' disease Hermansky-Pudlak syndrome 5 Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Lown-Ganong-Levine syndrome Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pelger-Huet anomaly Peutz-Jeghers syndrome Pick's disease Reye syndrome Sjogren's syndrome T-cell acute lymphoblastic leukemia Timothy syndrome Van der Woude syndrome Werner syndrome Wolff-Parkinson-White syndrome Zollinger-Ellison syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute myocarditis adenocarcinoma adenoma adrenoleukodystrophy adult acute lymphocytic leukemia adult acute monocytic leukemia amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome 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 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 basal cell carcinoma bilirubin metabolic disorder bladder carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease central nervous system cancer cerebral degeneration cerebral infarction cerebral malaria cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood leukemia childhood osteosarcoma cholestasis chondrosarcoma chromophobe renal cell carcinoma chronic kidney disease chronic myeloid leukemia clear cell renal cell carcinoma cleidocranial dysplasia cocaine abuse cocaine dependence colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cryptococcosis cyclic hematopoiesis cystic fibrosis cystinosis cystitis dengue disease depressive disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diarrhea diffuse large B-cell lymphoma dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dissociative amnesia distal myopathy early infantile epileptic encephalopathy embryoma endocrine exophthalmos endometrial cancer endometrial carcinoma endomyocardial fibrosis esophageal cancer esophageal carcinoma essential hypertension facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial periodic paralysis fibromyalgia gallbladder disease gastric adenocarcinoma gastroenteritis gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucose intolerance granular cell carcinoma gyrate atrophy head and neck squamous cell carcinoma heart disease hematologic cancer hepatitis B hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease humeroradial synostosis hyperglycemia hyperinsulinism hyperkalemic periodic paralysis hypertension hyperthyroidism hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy hypoglycemia hypokalemic periodic paralysis hypothyroidism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease inflammatory and toxic neuropathy inflammatory bowel disease influenza invasive ductal carcinoma islet cell tumor keratoconjunctivitis sicca kidney disease kidney failure large intestine cancer laryngeal squamous cell carcinoma leishmaniasis leukemia limb-girdle muscular dystrophy liver cancer liver carcinoma liver cirrhosis liver disease long QT syndrome 8 lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoblastic lymphoma lysosomal storage disease malignant pleural mesothelioma megaconial type congenital muscular dystrophy melanoma middle cerebral artery infarction mitral valve insufficiency mitral valve prolapse mixed glioma multiple myeloma muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myocardial infarction myopathy myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 myxedema nasopharynx carcinoma nemaline myopathy nephritis nephrogenic diabetes insipidus nephrosis neuroblastoma neurodegenerative disease nonpapillary renal cell carcinoma nutmeg liver obesity obsolete Opitz-GBBB 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 obstructive sleep apnea oculopharyngeal muscular dystrophy optic atrophy 1 optic atrophy osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma overnutrition pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary renal cell carcinoma pituitary adenoma pituitary cancer pituitary carcinoma placental insufficiency polycystic kidney disease 1 polycystic ovary syndrome postinflammatory pulmonary fibrosis postural orthostatic tachycardia syndrome prediabetes syndrome primary pulmonary hypertension prion disease progeria prostate cancer prostate carcinoma pulmonary fibrosis pyoureter radioulnar synostosis renal carcinoma renal cell carcinoma retrograde amnesia rigid spine muscular dystrophy 1 sarcomatoid carcinoma sarcomatoid renal cell carcinoma sick sinus syndrome silent myocardial infarction situs inversus skin melanoma spindle cell hemangioma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma synovitis systemic lupus erythematosus tauopathy tenosynovitis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma trigonitis 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 ureteral obstruction urinary bladder cancer uterine corpus cancer vascular disease viral infectious disease visceral leishmaniasis von Hippel-Lindau disease yellow fever
A8MYU2	Potassium channel subfamily U member 1	KCNU1 KCNMA3 KCNMC1 SLO3	Homo sapiens (human)	2	4
Q6IEE7	Transmembrane protein 132E	TMEM132E	Homo sapiens (human)	7	4
Q13286	Battenin	CLN3 BTS	Homo sapiens (human)	4	4
P11142	Heat shock cognate 71 kDa protein	HSPA8 HSC70 HSP73 HSPA10	Homo sapiens (human)	8	4
Q9H2Y7	Zinc finger protein 106	ZNF106 SH3BP3 ZFP106 ZNF474	Homo sapiens (human)	8	4
P53794	Sodium/myo-inositol cotransporter	SLC5A3	Homo sapiens (human)	2	4
P38398	Breast cancer type 1 susceptibility protein	BRCA1 RNF53	Homo sapiens (human)	2	4
P16989	Y-box-binding protein 3	YBX3 CSDA DBPA	Homo sapiens (human)	5	4
P08514	Integrin alpha-IIb	ITGA2B GP2B ITGAB	Homo sapiens (human)	9	4
Q8IWB1	Inositol 1,4,5-trisphosphate receptor-interacting protein	ITPRIP DANGER KIAA1754	Homo sapiens (human)	3	4
O43660	Pleiotropic regulator 1	PLRG1	Homo sapiens (human)	6	4
Q16819	Meprin A subunit alpha	MEP1A	Homo sapiens (human)	8	4
Q9BQF6	Sentrin-specific protease 7	SENP7 KIAA1707 SSP2 SUSP2	Homo sapiens (human)	2	4
Q9Y4P3	Transducin beta-like protein 2	TBL2 WBSCR13	Homo sapiens (human)	3	4

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