GlyCosmos Portal

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Displaying entries **9801 - 9825** 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
Q9H1Z4	WD repeat-containing protein 13	WDR13	Homo sapiens (human)	1	1
Q9H1Y3	Opsin-3	OPN3 ECPN	Homo sapiens (human)	2	0
Q9H1Y0	Autophagy protein 5	ATG5 APG5L ASP	Homo sapiens (human)	0	1
Q9H1X1	Radial spoke head protein 9 homolog	RSPH9 C6orf206 MRPS18AL1	Homo sapiens (human)	0	1
Q9H1V8	Sodium-dependent neutral amino acid transporter SLC6A17	SLC6A17 NTT4	Homo sapiens (human)	4	3
Q9H1U4	Multiple epidermal growth factor-like domains protein 9	MEGF9 EGFL5 KIAA0818	Homo sapiens (human)	16	2
Q9H1N7	Adenosine 3'-phospho 5'-phosphosulfate transporter 2	SLC35B3 C6orf196 PAPST2	Homo sapiens (human)	3	0	diabetes mellitus type 2 diabetes mellitus
Q9H1K1	Iron-sulfur cluster assembly enzyme ISCU	ISCU NIFUN	Homo sapiens (human)	0	1
Q9H1K0	Rabenosyn-5	RBSN ZFYVE20	Homo sapiens (human)	2	1
Q9H1J7	Protein Wnt-5b	WNT5B	Homo sapiens (human)	6	3
Q9H1J5	Protein Wnt-8a	WNT8A WNT8D	Homo sapiens (human)	3	0
Q9H1J1	Regulator of nonsense transcripts 3A	UPF3A RENT3A UPF3	Homo sapiens (human)	0	1
Q9H1I8	Activating signal cointegrator 1 complex subunit 2	ASCC2 ASC1P100 RQT3	Homo sapiens (human)	0	1
Q9H1H9	Kinesin-like protein KIF13A	KIF13A RBKIN	Homo sapiens (human)	2	1
Q9H1E5	Thioredoxin-related transmembrane protein 4	TMX4 KIAA1162 TXNDC13	Homo sapiens (human)	2	6
Q9H1E3	Nuclear ubiquitous casein and cyclin-dependent kinase substrate 1	NUCKS1 NUCKS	Homo sapiens (human)	0	1
Q9H1E1	Ribonuclease 7	RNASE7	Homo sapiens (human)	1	0
Q9H1D0	Transient receptor potential cation channel subfamily V member 6	TRPV6 ECAC2	Homo sapiens (human)	4	1
Q9H1C4	Protein unc-93 homolog B1	UNC93B1 UNC93 UNC93B	Homo sapiens (human)	4	0
Q9H1C3	Glycosyltransferase 8 domain-containing protein 2	GLT8D2 GALA4A	Homo sapiens (human)	1	0	hepatitis C liver cirrhosis
Q9H1C0	Lysophosphatidic acid receptor 5	LPAR5 GPR92 GPR93	Homo sapiens (human)	2	0
Q9H1B7	Probable E3 ubiquitin-protein ligase IRF2BPL	IRF2BPL C14orf4 EAP1 KIAA1865	Homo sapiens (human)	17	3
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
Q9H1A4	Anaphase-promoting complex subunit 1	ANAPC1 TSG24	Homo sapiens (human)	3	1
Q9H1A3	Protein-L-histidine N-pros-methyltransferase	METTL9 DREV	Homo sapiens (human)	1	6

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