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 **651 - 675** 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
P03393	Glycoprotein 55	env	Friend spleen focus-forming virus (isolate 502)	4	22
P02461	Collagen alpha-1(III) chain	COL3A1	Homo sapiens (human)	11	22
P48357	Leptin receptor	LEPR DB OBR	Homo sapiens (human)	19	22
Q91XG7	Tubulointerstitial nephritis antigen	Tinag	Mus musculus (house mouse)	4	22
Q9P273	Teneurin-3	TENM3 KIAA1455 ODZ3 TNM3	Homo sapiens (human)	24	22
Q8TAX7	Mucin-7	MUC7 MG2	Homo sapiens (human)	10	22
Q13641	Trophoblast glycoprotein	TPBG 5T4	Homo sapiens (human)	8	22
P17342	Atrial natriuretic peptide receptor 3	NPR3 ANPRC C5orf23 NPRC	Homo sapiens (human)	6	22
Q6UXD5	Seizure 6-like protein 2	SEZ6L2 PSK	Homo sapiens (human)	26	22
P15309	Prostatic acid phosphatase	ACP3 ACPP	Homo sapiens (human)	3	22
O75718	Cartilage-associated protein	CRTAP CASP	Homo sapiens (human)	5	22
Q9UHX3	Adhesion G protein-coupled receptor E2	ADGRE2 EMR2	Homo sapiens (human)	14	21
P17047	Lysosome-associated membrane glycoprotein 2	Lamp2 Lamp-2	Mus musculus (house mouse)	17	21
Q6GTX8	Leukocyte-associated immunoglobulin-like receptor 1	LAIR1 CD305	Homo sapiens (human)	2	21
P02668	Kappa-casein	CSN3 CSN10 CSNK	Bos taurus (cattle)	8	21
Q12860	Contactin-1	CNTN1	Homo sapiens (human)	11	21	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 Compton-North congenital myopathy Guillain-Barre syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome adenocarcinoma adenoma arthritis arthropathy attention deficit hyperactivity disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy colorectal cancer colorectal carcinoma congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A craniosynostosis cribriform carcinoma embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis familial nephrotic syndrome familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome gliosarcoma granular cell carcinoma high grade glioma islet cell tumor large intestine cancer lipoid nephrosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma megaconial type congenital muscular dystrophy membranous glomerulonephritis mixed glioma multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myopathy nemaline myopathy nephrotic syndrome neuropathy peripheral nervous system disease placental insufficiency polyhydramnios polyneuropathy progressive muscular atrophy prostate cancer prostate carcinoma rigid spine muscular dystrophy 1 spinal muscular atrophy squamous cell carcinoma stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma tubular adenocarcinoma
P04843	Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1	RPN1	Homo sapiens (human)	13	21	Burkitt lymphoma acute myeloid leukemia arteriosclerotic cardiovascular disease atherosclerosis childhood leukemia chronic kidney disease coronary artery disease leukemia nutmeg liver
Q6UY14	ADAMTS-like protein 4	ADAMTSL4 TSRC1	Homo sapiens (human)	19	21
Q9UBR2	Cathepsin Z	CTSZ	Homo sapiens (human)	2	21
P02452	Collagen alpha-1(I) chain	COL1A1	Homo sapiens (human)	15	21
Q9NY97	N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2	B3GNT2 B3GALT7 B3GNT1	Homo sapiens (human)	8	21	Graves' disease Walker-Warburg syndrome acute myocardial infarction cancer congenital muscular dystrophy-dystroglycanopathy type A1 coronary thrombosis hyperthyroidism myocardial infarction parapsoriasis prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole schizophrenia silent myocardial infarction thyrotoxicosis transitional cell carcinoma
O94769	Extracellular matrix protein 2	ECM2	Homo sapiens (human)	6	21
Q9Y6X5	Bis(5'-adenosyl)-triphosphatase ENPP4	ENPP4 KIAA0879 NPP4	Homo sapiens (human)	9	21
P01889	HLA class I histocompatibility antigen, B alpha chain	HLA-B HLAB	Homo sapiens (human)	2	21
O14594	Neurocan core protein	NCAN CSPG3 NEUR	Homo sapiens (human)	9	21	adrenoleukodystrophy alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alexia alternating hemiplegia of childhood attention deficit hyperactivity disorder autonomic neuropathy bipolar I disorder bipolar disorder bladder carcinoma brain disease cancer central nervous system disease depressive disorder dyslexia hepatitis C hepatitis hepatocellular carcinoma kidney failure liver cancer liver cirrhosis major depressive disorder melancholic depression morbid obesity multiple sclerosis nervous system disease neuroblastoma neuropathy neurotic disorder normal pressure hydrocephalus obsolete melancholia peripheral nervous system disease polyneuropathy schizophrenia steatotic liver disease urinary bladder cancer

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