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 **15601 - 15625** 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
Q8NA72	Centrosomal protein POC5	POC5 C5orf37	Homo sapiens (human)	1	2
O43674	NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 5, mitochondrial	NDUFB5	Homo sapiens (human)	1	2
Q05397	Focal adhesion kinase 1	PTK2 FAK FAK1	Homo sapiens (human)	2	2
Q8IWZ8	SURP and G-patch domain-containing protein 1	SUGP1 SF4	Homo sapiens (human)	8	2
Q460N5	Protein mono-ADP-ribosyltransferase PARP14	PARP14 BAL2 KIAA1268	Homo sapiens (human)	2	2	allergic asthma asthma cancer depressive disorder diffuse large B-cell lymphoma embryoma hepatocellular carcinoma intrinsic asthma liver cancer major depressive disorder melancholic depression multiple myeloma neurotic disorder obsolete melancholia pancreatic cancer pancreatic carcinoma
P16473	Thyrotropin receptor	TSHR LGR3	Homo sapiens (human)	6	2
Q9UKA9	Polypyrimidine tract-binding protein 2	PTBP2 NPTB PTB PTBLP	Homo sapiens (human)	1	2
Q8N7C4	Transmembrane protein 217	TMEM217 C6orf128	Homo sapiens (human)	3	2
Q9UBK2	Peroxisome proliferator-activated receptor gamma coactivator 1-alpha	PPARGC1A LEM6 PGC1 PGC1A PPARGC1	Homo sapiens (human)	1	2
Q9H1B5	Xylosyltransferase 2	XYLT2 XT2	Homo sapiens (human)	19	2	Cockayne syndrome Cornelia de Lange syndrome Desbuquois dysplasia Dubowitz syndrome Ewing sarcoma Gilbert syndrome Meckel 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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome T-cell acute lymphoblastic leukemia X-linked Aarskog syndrome acute biphenotypic leukemia acute leukemia acute myocardial infarction age related macular degeneration amblyopia angioid streaks ataxia telangiectasia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant polycystic kidney disease autosomal recessive Robinow syndrome bacterial infectious disease bilirubin metabolic disorder bladder carcinoma blindness brain stem infarction cancer cannabis abuse cannabis dependence cataract cerebral artery occlusion cerebral infarction cerebrovascular disease cholera chondrodysplasia-pseudohermaphroditism syndrome chronic kidney disease chronic monocytic leukemia chronic myelomonocytic leukemia clubfoot congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital nystagmus congestive heart failure coronary thrombosis degeneration of macula and posterior pole depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus dysthymic disorder embryoma essential hypertension gallbladder disease glomerulonephritis hepatic veno-occlusive disease hepatitis B herpes simplex hypertension intellectual disability intermittent claudication juvenile myelomonocytic leukemia keratosis follicularis kidney disease kidney failure learning disability lichen disease lipoatrophic diabetes mellitus lipodystrophy liver disease localized scleroderma macular degeneration major depressive disorder melancholic depression microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microphthalmia mitral valve insufficiency mitral valve prolapse mitral valve stenosis mongolian spot myocardial infarction myopia nephritis nephrosis neurotic disorder obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 osteoporosis papilloma patent foramen ovale pathologic nystagmus pleomorphic adenoma pneumocystosis postural orthostatic tachycardia syndrome pseudoxanthoma elasticum psoriatic arthritis pyoureter restrictive cardiomyopathy retinal detachment scleroderma sensorineural hearing loss silent myocardial infarction skin benign neoplasm skin cancer spontaneous ocular nystagmus squamous cell papilloma steatotic liver disease strabismic amblyopia systemic scleroderma thrombocytopenia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome 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 urinary bladder cancer ventricular septal defect viral infectious disease xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
P12272	Parathyroid hormone-related protein	PTHLH PTHRP	Homo sapiens (human)	3	2
Q14119	Vascular endothelial zinc finger 1	VEZF1 DB1 ZNF161	Homo sapiens (human)	24	2
Q8N228	Sex comb on midleg-like protein 4	SCML4	Homo sapiens (human)	2	2
Q9BQ69	ADP-ribose glycohydrolase MACROD1	MACROD1 LRP16	Homo sapiens (human)	1	2	acute monocytic leukemia atypical chronic myeloid leukemia, BCR-ABL1 negative bipolar disorder breast cancer breast carcinoma cancer cardiovascular system disease childhood leukemia chronic monocytic leukemia colorectal cancer colorectal carcinoma disease of metabolism embryoma endometrial cancer endometrial carcinoma gout heart disease hepatocellular carcinoma large intestine cancer leukemia liver cancer lymphoid leukemia monocytic leukemia myeloid leukemia nicotine dependence pancreatic cancer pancreatic carcinoma prolactinoma uterine corpus cancer
Q6P996	Pyridoxal-dependent decarboxylase domain-containing protein 1	PDXDC1 KIAA0251	Homo sapiens (human)	3	2
Q08AF3	Schlafen family member 5	SLFN5	Homo sapiens (human)	2	2
P46937	Transcriptional coactivator YAP1	YAP1 YAP65	Homo sapiens (human)	10	2
Q9BVA6	Protein adenylyltransferase FICD	FICD HIP13 HYPE	Homo sapiens (human)	2	2
P17535	Transcription factor JunD	JUND	Homo sapiens (human)	5	2
O95747	Serine/threonine-protein kinase OSR1	OXSR1 KIAA1101 OSR1	Homo sapiens (human)	2	2
P49593	Protein phosphatase 1F	PPM1F KIAA0015 POPX2	Homo sapiens (human)	3	2
Q8WWF1	Uncharacterized protein C1orf54	C1orf54	Homo sapiens (human)	2	2
Q9C0I3	Serine-rich coiled-coil domain-containing protein 1	CCSER1 FAM190A KIAA1680	Homo sapiens (human)	2	2
P63104	14-3-3 protein zeta/delta	YWHAZ	Homo sapiens (human)	2	2
O43399	Tumor protein D54	TPD52L2	Homo sapiens (human)	7	2

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