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 **4351 - 4375** 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
Q8N7C4	Transmembrane protein 217	TMEM217 C6orf128	Homo sapiens (human)	3	2
Q8CGK7	Guanine nucleotide-binding protein G(olf) subunit alpha	Gnal	Mus musculus (house mouse)	2	2
Q9UBK2	Peroxisome proliferator-activated receptor gamma coactivator 1-alpha	PPARGC1A LEM6 PGC1 PGC1A PPARGC1	Homo sapiens (human)	1	2
P27424	Microfibrillar-associated protein 2	MFAP2 MAGP MAGP1	Bos taurus (cattle)	0	2
O70433	Four and a half LIM domains protein 2	Fhl2	Mus musculus (house mouse)	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
Q9D0D4	Probable dimethyladenosine transferase	Dimt1 Dimt1l	Mus musculus (house mouse)	1	2
Q6P996	Pyridoxal-dependent decarboxylase domain-containing protein 1	PDXDC1 KIAA0251	Homo sapiens (human)	3	2
Q921U8	Smoothelin	Smtn Smsmo	Mus musculus (house mouse)	4	2
Q9DC69	NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9, mitochondrial	Ndufa9	Mus musculus (house mouse)	2	2
P23242	Gap junction alpha-1 protein	Gja1 Cxn-43	Mus musculus (house mouse)	1	2
Q08AF3	Schlafen family member 5	SLFN5	Homo sapiens (human)	2	2
Q3UHD6	Sorting nexin-27	Snx27 Kiaa0488	Mus musculus (house mouse)	1	2
P46937	Transcriptional coactivator YAP1	YAP1 YAP65	Homo sapiens (human)	10	2
Q9BVA6	Protein adenylyltransferase FICD	FICD HIP13 HYPE	Homo sapiens (human)	2	2
Q9CQ75	NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2	Ndufa2	Mus musculus (house mouse)	1	2
Q76M80	MNTK1	Kcnk12 mntk1	Mus musculus (house mouse)	1	2
P17535	Transcription factor JunD	JUND	Homo sapiens (human)	5	2
Q9Z108	Double-stranded RNA-binding protein Staufen homolog 1	Stau1 Stau	Mus musculus (house mouse)	1	2
Q80YA8	Protein crumbs homolog 2	Crb2	Mus musculus (house mouse)	13	2
O95747	Serine/threonine-protein kinase OSR1	OXSR1 KIAA1101 OSR1	Homo sapiens (human)	2	2

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