GlyCosmos Portal

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GlyConnect	April 19, 2023
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Displaying entries **16101 - 16125** 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
Q9H0Z9	RNA-binding protein 38	RBM38 RNPC1 SEB4	Homo sapiens (human)	1	1
Q9H106	Signal-regulatory protein delta	SIRPD PTPNS1L2	Homo sapiens (human)	1	0
Q9H112	Cystatin-11	CST11 CST8L	Homo sapiens (human)	1	0
Q9H114	Cystatin-like 1	CSTL1	Homo sapiens (human)	1	0
Q9H115	Beta-soluble NSF attachment protein	NAPB SNAPB	Homo sapiens (human)	0	1
Q9H116	GDNF-inducible zinc finger protein 1	GZF1 ZBTB23 ZNF336	Homo sapiens (human)	0	1
Q9H147	Deoxynucleotidyltransferase terminal-interacting protein 1	DNTTIP1 C20orf167 TDIF1	Homo sapiens (human)	1	1
Q9H156	SLIT and NTRK-like protein 2	SLITRK2 CXorf2 KIAA1854 SLITL1	Homo sapiens (human)	5	2
Q9H158	Protocadherin alpha-C1	PCDHAC1	Homo sapiens (human)	4	0
Q9H159	Cadherin-19	CDH19 CDH7L2	Homo sapiens (human)	8	0
Q9H160	Inhibitor of growth protein 2	ING2 ING1L	Homo sapiens (human)	0	1
Q9H161	Homeobox protein aristaless-like 4	ALX4 KIAA1788	Homo sapiens (human)	2	1
Q9H165	B-cell lymphoma/leukemia 11A	BCL11A CTIP1 EVI9 KIAA1809 ZNF856	Homo sapiens (human)	0	1
Q9H172	ATP-binding cassette sub-family G member 4	ABCG4 WHITE2	Homo sapiens (human)	1	0
Q9H173	Nucleotide exchange factor SIL1	SIL1	Homo sapiens (human)	16	12
Q9H175	Cysteine/serine-rich nuclear protein 2	CSRNP2 C12orf22 FAM130A1 TAIP12	Homo sapiens (human)	1	2
Q9H1A3	Protein-L-histidine N-pros-methyltransferase	METTL9 DREV	Homo sapiens (human)	1	6
Q9H1A4	Anaphase-promoting complex subunit 1	ANAPC1 TSG24	Homo sapiens (human)	3	1
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
Q9H1B7	Probable E3 ubiquitin-protein ligase IRF2BPL	IRF2BPL C14orf4 EAP1 KIAA1865	Homo sapiens (human)	17	3
Q9H1C0	Lysophosphatidic acid receptor 5	LPAR5 GPR92 GPR93	Homo sapiens (human)	2	0
Q9H1C3	Glycosyltransferase 8 domain-containing protein 2	GLT8D2 GALA4A	Homo sapiens (human)	1	0	hepatitis C liver cirrhosis
Q9H1C4	Protein unc-93 homolog B1	UNC93B1 UNC93 UNC93B	Homo sapiens (human)	4	0
Q9H1D0	Transient receptor potential cation channel subfamily V member 6	TRPV6 ECAC2	Homo sapiens (human)	4	1
Q9H1E1	Ribonuclease 7	RNASE7	Homo sapiens (human)	1	0

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