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 **5101 - 5125** 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
Q9BZE4	GTP-binding protein 4	GTPBP4 CRFG NOG1	Homo sapiens (human)	1	1
Q9NYZ3	G2 and S phase-expressed protein 1	GTSE1	Homo sapiens (human)	1	2
Q8WW33	Gametocyte-specific factor 1	GTSF1 FAM112B	Homo sapiens (human)	1	1
P33402	Guanylate cyclase soluble subunit alpha-2	GUCY1A2 GUC1A2 GUCSA2	Homo sapiens (human)	0	1
P25092	Guanylyl cyclase C	GUCY2C GUC2C STAR	Homo sapiens (human)	8	1
Q02846	Retinal guanylyl cyclase 1	GUCY2D CORD6 GUC1A4 GUC2D RETGC RETGC1	Homo sapiens (human)	2	1
Q8N442	Translation factor GUF1, mitochondrial	GUF1	Homo sapiens (human)	0	1
Q5J875	GUGU gamma form	GUGU	Homo sapiens (human)	1	0
Q9UBP9	PTB domain-containing engulfment adapter protein 1	GULP1 CED6 GULP	Homo sapiens (human)	1	1
P08236	Beta-glucuronidase	GUSB	Homo sapiens (human)	7	38	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 Clouston syndrome Crohn's colitis Crohn's disease De Quervain disease Fabry disease Laron syndrome Pick's disease Reye syndrome Richter's syndrome Sly syndrome Werner syndrome achondroplasia acute myeloid leukemia adenocarcinoma adenoma adenosarcoma adrenal gland cancer alcohol dependence alcohol use disorder alternating hemiplegia of childhood arteriosclerotic cardiovascular disease arteriovenous malformation arthritis arthropathy atherosclerosis autonomic neuropathy bladder carcinoma bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system disease cerebral degeneration cholecystolithiasis choledocholithiasis cholelithiasis chondrodysplasia punctata chronic lymphocytic leukemia chronic myeloid leukemia chylomicron retention disease clubfoot colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communicating hydrocephalus congestive heart failure coronary artery disease cystic fibrosis diabetes mellitus diabetic ketoacidosis diarrhea duodenum cancer elephantiasis embryoma endomyocardial fibrosis factor VIII deficiency familial adenomatous polyposis 1 familial adenomatous polyposis follicular adenoma gallbladder disease gastroenteritis gastrointestinal system disease gingival hypertrophy gingival overgrowth glycoproteinosis head and neck cancer head and neck squamous cell carcinoma heart cancer hepatitis B hepatitis C hepatitis hepatocellular carcinoma herpes simplex hydrocephalus hyperglycemia hypertrichosis hypertrophic cardiomyopathy ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intestinal disease islet cell tumor large intestine cancer learning disability lipid storage disease liver cancer liver disease lung adenocarcinoma lung cancer lung carcinoma lymphedema lysosomal storage disease microcystic adenoma mucolipidosis II alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myeloproliferative neoplasm nasopharynx carcinoma nephroblastoma nervous system disease neuroblastoma neurodegenerative disease obstructive hydrocephalus omphalocele ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma paraganglioma pheochromocytoma progeria prostate cancer prostate carcinoma proteinuria pulmonary tuberculosis recurrent corneal erosion retinal disease retinitis rheumatoid arthritis sarcomatoid carcinoma schizophrenia scoliosis senile degeneration of brain sensorineural hearing loss shigellosis small intestine cancer stomach cancer stomach carcinoma subacute thyroiditis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tuberculosis tuberculous pneumothorax type 2 diabetes mellitus ulcerative colitis umbilical hernia urinary bladder cancer
Q6P575	Putative inactive beta-glucuronidase protein GUSBP11	GUSBP11	Homo sapiens (human)	1	1
Q7Z2Y8	Interferon-induced very large GTPase 1	GVINP1 GVIN1 VLIG1	Homo sapiens (human)	3	1
Q3ZCU0	Protein GVQW3	GVQW3	Homo sapiens (human)	0	1
Q4G148	Glucoside xylosyltransferase 1	GXYLT1 GLT8D3	Homo sapiens (human)	6	13
A0PJZ3	Glucoside xylosyltransferase 2	GXYLT2 GLT8D4	Homo sapiens (human)	2	0
P46976	Glycogenin-1	GYG1 GYG	Homo sapiens (human)	1	1	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Lafora disease cardiomyopathy catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia central nervous system origin vertigo coronary artery disease cystinuria diabetes mellitus disease of metabolism endomyocardial fibrosis familial periodic paralysis galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease XV glycogen storage disease hypertrophic cardiomyopathy myopathy sick sinus syndrome type 2 diabetes mellitus
O15488	Glycogenin-2	GYG2	Homo sapiens (human)	1	0	Leigh disease cystinuria galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease
P02724	Glycophorin-A	GYPA GPA	Homo sapiens (human)	19	30
P06028	Glycophorin-B	GYPB GPB	Homo sapiens (human)	4	13
B8Q179	Glycophorin B Miltenberger subtype III	GYPB	Homo sapiens (human)	0	5
P04921	Glycophorin-C	GYPC GLPC GPC	Homo sapiens (human)	15	15
P13807	Glycogen [starch] synthase, muscle	GYS1 GYS	Homo sapiens (human)	2	1	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease abdominal obesity-metabolic syndrome 1 acute myocardial infarction arthritis arthropathy cardiomyopathy coronary thrombosis diabetes mellitus diabetic ketoacidosis endomyocardial fibrosis essential thrombocythemia hypertrophic cardiomyopathy hypoglycemia myelodysplastic syndrome myocardial infarction obsolete type 1 diabetes mellitus 9 rheumatoid arthritis silent myocardial infarction 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 visual epilepsy
P54840	Glycogen [starch] synthase, liver	GYS2	Homo sapiens (human)	1	1	Baraitser-Winter syndrome Fraser syndrome Gerstmann-Straussler-Scheinker syndrome Goldenhar syndrome Gorham's disease Joubert syndrome 1 Joubert syndrome Laron syndrome Moebius syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome achondroplasia adult medulloblastoma branchiootic syndrome cancer childhood medulloblastoma cystinuria disease of metabolism epilepsy familial hyperlipidemia galactosemia gestational diabetes glucosephosphate dehydrogenase deficiency glycogen storage disease III glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatitis B hepatocellular carcinoma hyperglycemia hypoglycemia liver cancer medulloblastoma medullomyoblastoma melanotic medulloblastoma orofaciodigital syndrome I orofaciodigital syndrome X orofaciodigital syndrome polycystic ovary syndrome visual epilepsy
Q9H116	GDNF-inducible zinc finger protein 1	GZF1 ZBTB23 ZNF336	Homo sapiens (human)	0	1
P12544	Granzyme A	GZMA CTLA3 HFSP	Homo sapiens (human)	1	8

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