GlyCosmos Portal

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GlyConnect	April 19, 2023
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The O-GlcNAc Database	June 3, 2024
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Displaying entries **120451 - 120475** 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
Q99584	Protein S100-A13	S100A13	Homo sapiens (human)	0	1
P30419	Glycylpeptide N-tetradecanoyltransferase 1	NMT1 NMT	Homo sapiens (human)	0	1
Q9CY16	Small ribosomal subunit protein bS1m	Mrps28	Mus musculus (house mouse)	0	1
A0A0A6YX26	Large ribosomal subunit protein eL31	Rpl31	Mus musculus (house mouse)	0	1
A1A6K6	Nuclear speckle RNA-binding protein A	NSRA	Arabidopsis thaliana (thale cress)	0	1
P11884	Aldehyde dehydrogenase, mitochondrial	Aldh2	Rattus norvegicus (Norway rat)	2	1
V5BI09	Sec1 family transport protein	TCDM_07923	Trypanosoma cruzi Dm28c	0	1
P09897	Large ribosomal subunit protein eL18A	rpl18-a rpl14a	Xenopus laevis (African clawed frog)	0	1
O00308	NEDD4-like E3 ubiquitin-protein ligase WWP2	WWP2	Homo sapiens (human)	0	1
Q5JY77	G-protein coupled receptor-associated sorting protein 1	GPRASP1 GASP KIAA0443	Homo sapiens (human)	0	1
Q91YT0	NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial	Ndufv1	Mus musculus (house mouse)	0	1
Q9UHF7	Zinc finger transcription factor Trps1	TRPS1	Homo sapiens (human)	4	1
V5B6G9	Aconitate hydratase	TCDM_02343	Trypanosoma cruzi Dm28c	0	1
P11498	Pyruvate carboxylase, mitochondrial	PC	Homo sapiens (human)	1	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 Burkitt lymphoma Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Langerhans-cell histiocytosis Pick's disease Reye syndrome Sjogren's syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction adult fibrosarcoma alcohol dependence alcohol use disorder allergic asthma antiphospholipid syndrome antithrombin III deficiency anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis attention deficit hyperactivity disorder autistic disorder autoimmune polyendocrine syndrome autosomal dominant familial periodic fever bacterial sepsis beta thalassemia bipolar disorder blood coagulation disease breast cancer breast carcinoma cancer cardiovascular system disease cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma colitis congenital afibrinogenemia coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis disseminated intravascular coagulation embryoma enterobiasis epilepsy essential hypertension factor V deficiency factor VII deficiency familial hyperlipidemia fibrosarcoma gallbladder cancer gallbladder carcinoma gastroenteritis generalized anxiety disorder glomerulonephritis heart disease hemoglobin H disease hepatitis hepatocellular carcinoma holocarboxylase synthetase deficiency hyperglycemia hyperhomocysteinemia hyperlysinemia hypertension hyperthyroidism hyperuricemia hypoglycemia ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome inflammatory bowel disease intellectual disability intestinal schistosomiasis intracranial sinus thrombosis ischemic colitis keratoconjunctivitis sicca kidney disease kwashiorkor lactic acidosis learning disability leukodystrophy liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lupus erythematosus lymphoma malignant exocrine pancreas neoplasm marasmus melanoma multiple sclerosis myocardial infarction nephritis nephrosis non-Hodgkin lymphoma nutrition disease obesity obsolete inherited blood coagulation disease obsolete ymphosarcoma papillary adenocarcinoma papillary renal cell carcinoma periventricular leukomalacia phobic disorder portal vein thrombosis protein C deficiency protein S deficiency protein-energy malnutrition purpura fulminans pyoureter pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency renal tubular acidosis reticulosarcoma schistosomiasis silent myocardial infarction skin melanoma steatotic liver disease synovial sarcoma systemic lupus erythematosus thalassemia thrombophilia thyroid gland papillary carcinoma thyrotoxicosis trichinosis tuberculosis type 2 diabetes mellitus urea cycle disorder visual epilepsy vitamin K deficiency bleeding
V5B4D8	TATA-binding protein interacting (TIP20) domain-containing protein	TCDM_03179	Trypanosoma cruzi Dm28c	0	1
Q9BWT6	Meiotic nuclear division protein 1 homolog	MND1 GAJ	Homo sapiens (human)	1	1
Q63450	Calcium/calmodulin-dependent protein kinase type 1	Camk1	Rattus norvegicus (Norway rat)	0	1
K7SWG8	adenylate cyclase	C4B63_14g22	Trypanosoma cruzi	0	1
D3YWK1	WD repeat domain phosphoinositide-interacting protein 2	Wipi2	Mus musculus (house mouse)	0	1
V5BLI8	Cytoskeleton associated protein	TCDM_02558	Trypanosoma cruzi Dm28c	0	1
P34949	Mannose-6-phosphate isomerase	MPI PMI1	Homo sapiens (human)	0	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 Pick's disease Reye syndrome Zollinger-Ellison syndrome acute myeloid leukemia acute myocardial infarction antithrombin III deficiency anxiety disorder arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant cerebellar ataxia autosomal recessive hypercholesterolemia autosomal recessive polycystic kidney disease blindness blood coagulation disease campomelic dysplasia cancer cardiovascular system disease celiac disease central nervous system cancer cerebral degeneration chronic kidney disease congenital disorder of glycosylation Ia congenital disorder of glycosylation Ib congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congestive heart failure coronary artery disease coronary thrombosis craniometaphyseal dysplasia cryptococcosis cystic fibrosis developmental and epileptic encephalopathy 36 diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy dry eye syndrome egg allergy elephantiasis embryoma epilepsy essential hypertension familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 gallbladder disease generalized anxiety disorder gliosarcoma heart disease hepatitis B high grade glioma hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia laryngeal disease liver cirrhosis liver disease lymphedema marasmus mixed glioma myocardial infarction neurotic disorder nutmeg liver obsolete inherited blood coagulation disease phobic disorder placental insufficiency polycystic kidney disease 4 post-traumatic stress disorder postpartum depression protein C deficiency protein S deficiency protein-losing enteropathy schizophrenia silent myocardial infarction spinocerebellar ataxia type 6 steatotic liver disease thrombocytopenia thrombophilia tracheal disease tropical sprue type 2 diabetes mellitus visual epilepsy xerophthalmia
O00165	HCLS1-associated protein X-1	HAX1 HS1BP1	Homo sapiens (human)	1	1
P02666	Beta-casein	CSN2	Bos taurus (cattle)	0	1
Q6GV06	IP20609p (Fragment)	lectin-30A AC 005889A AC005889a CG17011-RA Dmel\CG17011 Lectin-30A Lectin30A	Drosophila melanogaster (fruit fly)	0	1
A0A125YII2	60S ribosomal protein L13	TGVEG_263050	Toxoplasma gondii VEG	0	1

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