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 **125851 - 125875** 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
O95479	GDH/6PGL endoplasmic bifunctional protein	H6PD GDH	Homo sapiens (human)	3	20	Alzheimer's disease B-cell lymphoma Laron syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis beta thalassemia breast cancer breast carcinoma cancer cardiovascular system disease cholangiocarcinoma colorectal cancer cone-rod dystrophy 2 cone-rod dystrophy coronary artery disease cortisone reductase deficiency 1 cortisone reductase deficiency dementia diabetes insipidus diabetes mellitus diabetic ketoacidosis diarrhea gallbladder disease giardiasis heart disease hemolytic anemia hyperandrogenism hyperinsulinism hypertrichosis hypoglycemia infertility intrahepatic cholangiocarcinoma large intestine cancer leishmaniasis liver disease luminal breast carcinoma A malaria multiple sclerosis neurohypophyseal diabetes insipidus obesity obsolete ymphosarcoma placental insufficiency polycystic ovary syndrome primary hyperoxaluria steatotic liver disease thalassemia type 2 diabetes mellitus visceral leishmaniasis
O35405	5'-3' exonuclease PLD3	Pld3 Sam9	Mus musculus (house mouse)	4	20
O88998	Noelin	Olfm1 Noe1 Noel Noel1	Mus musculus (house mouse)	12	20
Q01097	Glutamate receptor ionotropic, NMDA 2B	Grin2b	Mus musculus (house mouse)	17	20
Q01459	Di-N-acetylchitobiase	CTBS CTB	Homo sapiens (human)	4	20	Clouston syndrome allergic rhinitis amyotrophic lateral sclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer cholera colon cancer colon carcinoma colonic benign neoplasm colorectal cancer hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease large intestine cancer liver cancer progressive muscular atrophy prostate cancer prostate carcinoma ulcerative colitis vasomotor rhinitis
Q9UJJ9	N-acetylglucosamine-1-phosphotransferase subunit gamma	GNPTG C16orf27 GNPTAG	Homo sapiens (human)	11	20	Fabry disease Laron syndrome achondroplasia alexia aortic valve disease 2 aortic valve insufficiency aortic valve stenosis chylomicron retention disease cone-rod dystrophy dyslexia fundus albipunctatus glycoproteinosis lipid storage disease lysosomal storage disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myopia osteochondrodysplasia retinitis pigmentosa scoliosis stuttering
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
P39060	Collagen alpha-1(XVIII) chain	COL18A1	Homo sapiens (human)	37	21
Q16880	2-hydroxyacylsphingosine 1-beta-galactosyltransferase	UGT8 CGT UGT4	Homo sapiens (human)	5	21	Barrett's esophagus GM2 gangliosidosis adenocarcinoma adenoma adult oligodendroglioma adult respiratory distress syndrome allergic rhinitis anthracosilicosis anthracosis asbestosis brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer childhood oligodendroglioma classic galactosemia congenital hemolytic anemia cribriform carcinoma cystinuria dilated cardiomyopathy 1A dilated cardiomyopathy embryoma epilepsy esophagus adenocarcinoma favism galactokinase deficiency galactosemia gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease granular cell carcinoma hepatocellular carcinoma hereditary elliptocytosis high grade glioma liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma mixed glioma mixed oligodendroglioma-astrocytoma myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 newborn respiratory distress syndrome oligodendroglioma pancreatic cancer pancreatic carcinoma parapsoriasis parietal foramina prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole skin melanoma split hand-foot malformation 1 split hand-foot malformation 2 split hand-foot malformation 3 split hand-foot malformation 4 split hand-foot malformation 5 split hand-foot malformation 6 split hand-foot malformation tubular adenocarcinoma vasomotor rhinitis visual epilepsy
Q8WXD2	Secretogranin-3	SCG3	Homo sapiens (human)	10	21
P26927	Hepatocyte growth factor-like protein	MST1 D3F15S2 DNF15S2 HGFL	Homo sapiens (human)	6	21
Q9UBX1	Cathepsin F	CTSF	Homo sapiens (human)	5	21

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