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 **2601 - 2625** 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
P20933	N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase	AGA	Homo sapiens (human)	4	11	Clostridium difficile colitis Down syndrome Fabry disease Klippel-Feil syndrome Laron syndrome abdominal obesity-metabolic syndrome 1 achalasia achondroplasia acne acrodermatitis agranulocytosis alcoholic hepatitis allergic bronchopulmonary aspergillosis alopecia androgenic alopecia arthritis arthropathy aspartylglucosaminuria attention deficit hyperactivity disorder cancer cataract celiac disease cerebral degeneration cervical squamous cell carcinoma cholecystitis chylomicron retention disease clubfoot common wart congenital disorder of glycosylation craniosynostosis dental caries dentin caries dermatitis herpetiformis diabetes mellitus diabetic ketoacidosis diarrhea dystonia encephalitis encephalomyelitis enterocele eosinophilic esophagitis epilepsy esophageal disease familial isolated hypoparathyroidism fucosidosis functional diarrhea gestational diabetes gingival hypertrophy gingival overgrowth goiter hepatitis C hepatocellular carcinoma hypoparathyroidism immunoglobulin alpha deficiency inflammatory bowel disease 1 inflammatory bowel disease influenza inguinal hernia intellectual disability irritable bowel syndrome learning disability lingual-facial-buccal dyskinesia lipid storage disease livedoid vasculitis liver cancer liver cirrhosis lupus nephritis lysosomal storage disease megaesophagus microcephaly mitral valve insufficiency mitral valve prolapse mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple sclerosis myelitis neurocirculatory asthenia neutropenia obsolete dyspepsia obsolete type 1 diabetes mellitus 9 omphalocele otitis media peroxisome biogenesis disorder 10A placental insufficiency primary sclerosing cholangitis schizoaffective disorder schizophrenia schizophreniform disorder sclerosing cholangitis scoliosis selective IgA deficiency disease severe congenital neutropenia skeletal tuberculosis speech disorder spondylolisthesis spondylolysis stomach cancer stomach carcinoma stomach disease thyroid gland disease tropical sprue tuberculosis 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 ulcerative colitis umbilical hernia vascular skin disease visual epilepsy
Q15393	Splicing factor 3B subunit 3	SF3B3 KIAA0017 SAP130	Homo sapiens (human)	4	3
O60828	Polyglutamine-binding protein 1	PQBP1 NPW38	Homo sapiens (human)	4	1
Q6UWM9	UDP-glucuronosyltransferase 2A3	UGT2A3	Homo sapiens (human)	4	19
Q96TA0	Putative protocadherin beta-18	PCDHB18P PCDHB18	Homo sapiens (human)	4	0
P30988	Calcitonin receptor	CALCR	Homo sapiens (human)	4	0
Q68EM7	Rho GTPase-activating protein 17	ARHGAP17 RICH1	Homo sapiens (human)	4	1
P22670	MHC class II regulatory factor RFX1	RFX1	Homo sapiens (human)	4	1
B5A930	Soluble MET variant 2	MET	Homo sapiens (human)	4	0
Q8TC56	Golgi-associated RAB2 interactor protein 3	GARIN3 FAM71B	Homo sapiens (human)	4	2
O95427	GPI ethanolamine phosphate transferase 1	PIGN MCD4	Homo sapiens (human)	4	8	Dandy-Walker syndrome Hirschsprung's disease Marfan syndrome Meckel syndrome Miller-Dieker lissencephaly syndrome Paget's disease of bone acute monocytic leukemia acute myeloid leukemia amblyopia 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 polycystic kidney disease basal ganglia disease blepharitis blepharospasm cerebral degeneration chromosome 17p13.1 deletion syndrome chronic recurrent multifocal osteomyelitis cleft palate colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congenital nystagmus cryptorchidism dissociated nystagmus duodenal atresia epilepsy esophagitis esotropia essential thrombocythemia focal hand dystonia gastroesophageal reflux disease gingival hypertrophy gingival overgrowth heart septal defect holoprosencephaly 1 holoprosencephaly hydrocephalus hydronephrosis hypospadias idiopathic interstitial pneumonia imperforate anus intellectual disability isolated cleft palate large intestine cancer learning disability lingual-facial-buccal dyskinesia lissencephaly lung adenocarcinoma lung cancer mammary Paget's disease microphthalmia monocular esotropia movement disease multiple congenital anomalies-hypotonia-seizures syndrome 1 myelodysplastic syndrome omphalocele patent ductus arteriosus patent foramen ovale pathologic nystagmus peptic esophagitis polyhydramnios postinflammatory pulmonary fibrosis primary pulmonary hypertension pulmonary fibrosis recurrent corneal erosion renal agenesis situs inversus spontaneous ocular nystagmus strabismic amblyopia tetralogy of Fallot tuberous sclerosis umbilical hernia vesicoureteral reflux visual epilepsy
Q9HCE3	Zinc finger protein 532	ZNF532 KIAA1629	Homo sapiens (human)	4	1
P58876	Histone H2B type 1-D	H2BC5 H2BFB HIRIP2 HIST1H2BD	Homo sapiens (human)	4	1
P35503	UDP-glucuronosyltransferase 1A3	UGT1A3 GNT1 UGT1	Homo sapiens (human)	4	41	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis allergic asthma asthma beta thalassemia bilirubin metabolic disorder breast cancer breast carcinoma cancer carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis cryptococcosis diabetes mellitus differentiated thyroid gland carcinoma embryoma epilepsy familial adenomatous polyposis 1 familial adenomatous polyposis gallbladder disease glycogen storage disease II hepatitis D influenza intrinsic asthma islet cell tumor leukopenia liver disease lung adenocarcinoma lung cancer neonatal jaundice neutropenia obesity pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma sarcomatoid carcinoma schizophrenia severe congenital neutropenia sickle cell anemia thalassemia type 2 diabetes mellitus visual epilepsy xeroderma pigmentosum group D
Q70E73	Ras-associated and pleckstrin homology domains-containing protein 1	RAPH1 ALS2CR18 ALS2CR9 KIAA1681 LPD PREL2 RMO1	Homo sapiens (human)	4	1
Q9HDB5	Neurexin-3-beta	NRXN3 KIAA0743	Homo sapiens (human)	4	0
P07550	Beta-2 adrenergic receptor	ADRB2 ADRB2R B2AR	Homo sapiens (human)	4	1
Q12907	Vesicular integral-membrane protein VIP36	LMAN2 C5orf8	Homo sapiens (human)	4	49	neuroblastoma stomach cancer stomach carcinoma
H0Y300	Haptoglobin	HP	Homo sapiens (human)	4	0
Q92628	Uncharacterized protein KIAA0232	KIAA0232	Homo sapiens (human)	4	9
Q07699	Sodium channel subunit beta-1	SCN1B	Homo sapiens (human)	4	0
Q6UWH4	Golgi-associated kinase 1B	GASK1B C4orf18 ENED FAM198B	Homo sapiens (human)	4	2
Q06413	Myocyte-specific enhancer factor 2C	MEF2C	Homo sapiens (human)	4	1
E9PFZ2	Ceruloplasmin	CP	Homo sapiens (human)	4	0
B5A933	Soluble MET variant 5	MET	Homo sapiens (human)	4	0

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