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 **2001 - 2025** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
O00488	Zinc finger protein 593	ZNF593 ZT86	Homo sapiens (human)	1
Q5VSR9	Sperm protein associated with the nucleus on the X chromosome N1	SPANXN1	Homo sapiens (human)	1
Q86W54	Spermatogenesis-associated protein 24	SPATA24	Homo sapiens (human)	1
Q8N7K0	Zinc finger protein 433	ZNF433	Homo sapiens (human)	1
Q86T90	Protein hinderin	KIAA1328	Homo sapiens (human)	1
Q4V339	Zinc-regulated GTPase metalloprotein activator 1F	ZNG1F CBWD6 CBWD7	Homo sapiens (human)	1
Q9Y4X5	E3 ubiquitin-protein ligase ARIH1	ARIH1 ARI MOP6 UBCH7BP	Homo sapiens (human)	1
Q6ZSJ8	Uncharacterized protein C1orf122	C1orf122	Homo sapiens (human)	1
Q8NEJ9	Neuroguidin	NGDN C14orf120	Homo sapiens (human)	1
P30613	Pyruvate kinase PKLR	PKLR PK1 PKL	Homo sapiens (human)	1	Gaucher's disease acquired polycythemia anemia breast cancer breast carcinoma cancer cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis colorectal cancer colorectal carcinoma congenital hemolytic anemia congenital nonspherocytic hemolytic anemia depressive disorder diabetes mellitus diabetic ketoacidosis episodic kinesigenic dyskinesia 1 erythropoietin polycythemia familial erythrocytosis 1 familial erythrocytosis 2 favism gallbladder cancer gallbladder carcinoma hematopoietic system disease hemoglobinopathy hemolytic anemia hepatocellular carcinoma hereditary elliptocytosis hereditary sensory neuropathy type 4 hereditary sensory neuropathy hyperglycemia large intestine cancer liver cancer lung benign neoplasm macrocytic anemia major depressive disorder malaria melancholic depression obsolete melancholia optic atrophy 1 optic atrophy pancreatic cancer pancreatic carcinoma polycythemia vera polycythemia primary polycythemia prostate cancer prostate carcinoma pyruvate kinase deficiency of red cells sensory peripheral neuropathy stress polycythemia thalassemia type 2 diabetes mellitus
Q13085	Acetyl-CoA carboxylase 1	ACACA ACAC ACC1 ACCA	Homo sapiens (human)	1	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 Bloch-Sulzberger syndrome Clouston syndrome Crohn's colitis Crohn's disease Graves' disease IgA glomerulonephritis Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Wernicke-Korsakoff syndrome Wilson disease Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute chest syndrome acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoid cystic carcinoma adenoma adrenal adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma adult respiratory distress syndrome agenesis of the corpus callosum with peripheral neuropathy allergic rhinitis amyotrophic lateral sclerosis type 1 ankyloblepharon-ectodermal defects-cleft lip/palate syndrome anorexia nervosa anxiety disorder aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy ataxia telangiectasia atherosclerosis atrophic gastritis attention deficit hyperactivity disorder atypical teratoid rhabdoid tumor autism spectrum disorder autistic disorder autoimmune hepatitis benign mesothelioma bipolar disorder brain stem infarction breast adenoid cystic carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma bulimia nervosa cancer carcinoma cardiomyopathy cardiovascular system disease celiac disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia chromophobe renal cell carcinoma chronic kidney disease chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma 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 depressive disorder diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism duodenum cancer dysthymic disorder embryoma endometriosis of uterus endometriosis endomyocardial fibrosis epidermal appendage tumor esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension familial hyperlipidemia familial hypertrophic cardiomyopathy familial periodic paralysis focal segmental glomerulosclerosis follicular adenoma gallbladder disease generalized anxiety disorder gestational diabetes giant cell glioblastoma gingivitis glioblastoma glomerulonephritis head and neck squamous cell carcinoma heart cancer heart disease heart valve disease hemochromatosis hepatitis B hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertension hyperthyroidism hypertrichosis hypertrophic cardiomyopathy hypohidrotic ectodermal dysplasia hypomelanosis of Ito inflammatory bowel disease 1 inflammatory bowel disease iron metabolism disease juvenile rheumatoid arthritis kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer leprosy leukemia liver cancer liver carcinoma liver disease luminal breast carcinoma A lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder malaria malignant mesothelioma malignant pleural mesothelioma megaconial type congenital muscular dystrophy melancholic depression microcystic adenoma middle cerebral artery infarction migraine mitochondrial metabolism disease mitochondrial myopathy mitral valve disease muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myocardial infarction myopathy nemaline myopathy nephritis nephrosis neuropathy neurotic disorder newborn respiratory distress syndrome non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsessive-compulsive disorder obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obsolete ymphosarcoma ovarian cancer ovarian carcinoma papillary adenoma papillary renal cell carcinoma paraganglioma parapsoriasis periodontitis peripheral nervous system disease peroxisome biogenesis disorder 7A pheochromocytoma phobic disorder placental insufficiency polycystic ovary syndrome polyneuropathy primary ovarian insufficiency prostate adenocarcinoma prostate cancer prostate carcinoma psoriasis psoriatic arthritis pulmonary tuberculosis pustulosis of palm and sole pyoureter renal carcinoma renal cell carcinoma reticulosarcoma rheumatoid arthritis rigid spine muscular dystrophy 1 salivary gland adenoid cystic carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia scleroderma seminoma silent myocardial infarction skin benign neoplasm skin cancer small intestine cancer steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder systemic lupus erythematosus systemic scleroderma testicular cancer testis seminoma thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland follicular carcinoma thyrotoxicosis trichuriasis tuberculosis tuberculous pneumothorax type 2 diabetes mellitus ulcerative colitis vasomotor rhinitis viral infectious disease visual epilepsy
Q9BR01	Sulfotransferase 4A1	SULT4A1 SULTX3	Homo sapiens (human)	1
Q6ZNA4	E3 ubiquitin-protein ligase Arkadia	RNF111	Homo sapiens (human)	1
E7ETM0	non-specific serine/threonine protein kinase	CSNK1A1	Homo sapiens (human)	1
P18077	Large ribosomal subunit protein eL33	RPL35A	Homo sapiens (human)	1
P15172	Myoblast determination protein 1	MYOD1 BHLHC1 MYF3 MYOD	Homo sapiens (human)	1
P29558	RNA-binding motif, single-stranded-interacting protein 1	RBMS1 C2orf12 MSSP MSSP1 SCR2	Homo sapiens (human)	1
Q96C00	Zinc finger and BTB domain-containing protein 9	ZBTB9	Homo sapiens (human)	1
Q9BTT4	Mediator of RNA polymerase II transcription subunit 10	MED10	Homo sapiens (human)	1
Q9Y4R8	Telomere length regulation protein TEL2 homolog	TELO2 KIAA0683	Homo sapiens (human)	1
P62714	Serine/threonine-protein phosphatase 2A catalytic subunit beta isoform	PPP2CB	Homo sapiens (human)	1
Q96QR8	Transcriptional regulator protein Pur-beta	PURB	Homo sapiens (human)	1
A5PLN9	Trafficking protein particle complex subunit 13	TRAPPC13 C5orf44	Homo sapiens (human)	1
Q92889	DNA repair endonuclease XPF	ERCC4 ERCC11 XPF	Homo sapiens (human)	1
Q9NQX1	PR domain zinc finger protein 5	PRDM5 PFM2	Homo sapiens (human)	1

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