GlyCosmos Portal

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GlyConnect	April 19, 2023
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GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **124776 - 124800** 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
Q8NBS9	Thioredoxin domain-containing protein 5	TXNDC5 TLP46	Homo sapiens (human)	14	6
E9PVD3	Protocadherin-16	Dchs1	Mus musculus (house mouse)	7	6
Q9JMB8	Contactin-6	Cntn6	Mus musculus (house mouse)	13	6
Q91YY2	Beta-1,4-galactosyltransferase 3	B4galt3	Mus musculus (house mouse)	4	6
Q9UJT0	Tubulin epsilon chain	TUBE1 TUBE	Homo sapiens (human)	1	6
F2Z4A3	FAT atypical cadherin 1	Fat1	Mus musculus (house mouse)	9	6
Q14157	Ubiquitin-associated protein 2-like	UBAP2L KIAA0144 NICE4	Homo sapiens (human)	105	6
O95857	Tetraspanin-13	TSPAN13 NET6 TM4SF13	Homo sapiens (human)	4	6
P49792	E3 SUMO-protein ligase RanBP2	RANBP2 NUP358	Homo sapiens (human)	68	6
Q61627	Glutamate receptor ionotropic, delta-1	Grid1	Mus musculus (house mouse)	7	6
Q6PIE5	Sodium/potassium-transporting ATPase subunit alpha-2	Atp1a2	Mus musculus (house mouse)	9	6
P13866	Sodium/glucose cotransporter 1	SLC5A1 NAGT SGLT1	Homo sapiens (human)	4	6	Bartter disease Conn's syndrome Fanconi syndrome Waterhouse-Friderichsen syndrome X-linked juvenile retinoschisis 1 abdominal obesity-metabolic syndrome 1 acute myocardial infarction adenocarcinoma adenoma arteriosclerotic cardiovascular disease atherosclerosis bacterial infectious disease bacterial sepsis brain stem infarction breast cancer breast carcinoma calcinosis calcium metabolism disease cancer cardiomyopathy cardiovascular system disease cerebral artery occlusion cerebral infarction cerebrovascular disease cholera colon adenocarcinoma congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cutaneous leishmaniasis cystinosis diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism embryoma endomyocardial fibrosis essential hypertension familial hypertrophic cardiomyopathy galactosemia glomerulonephritis glucose intolerance granular cell carcinoma heart disease hepatocellular carcinoma hypercalcemia hyperglycemia hypertension hypertrophic cardiomyopathy hypoglycemia intestinal atresia kidney disease kidney failure kwashiorkor lactic acidosis listeriosis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma marasmus middle cerebral artery infarction myocardial infarction nephritis nephrocalcinosis nephrosis nutmeg liver nutrition disease obesity obsolete type 1 diabetes mellitus 9 optic atrophy 1 optic atrophy pancreatic cancer pancreatic carcinoma phosphorus metabolism disease pneumonia prediabetes syndrome primary hyperaldosteronism protein-energy malnutrition pyoureter renal glycosuria silent myocardial infarction squamous cell carcinoma tongue squamous cell carcinoma toxic shock syndrome tropical sprue tubular adenocarcinoma 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
Q6Y288	Beta-1,3-glucosyltransferase	B3GLCT B3GALTL B3GTL	Homo sapiens (human)	3	6	Axenfeld-Rieger syndrome IGSF1 deficiency syndrome Klippel-Feil syndrome Kuhnt-Junius degeneration Meckel syndrome Peters anomaly Peters plus syndrome Tn polyagglutination syndrome age related macular degeneration anemia 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 autism spectrum disorder autistic disorder autosomal dominant polycystic kidney disease blindness cataract cerebral degeneration cleft lip cleft palate coloboma communicating hydrocephalus congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nystagmus congenital ptosis cornea plana craniosynostosis cryptorchidism degeneration of macula and posterior pole depressive disorder dissociated nystagmus epilepsy eye disease glaucoma heart septal defect hydrocephalus hydronephrosis hypoplastic left heart syndrome hypospadias hypothyroidism imperforate anus inguinal hernia intellectual disability isolated cleft palate learning disability macrocytic anemia macular degeneration major depressive disorder melancholic depression microcephaly myopia myxedema obsolete melancholia obstructive hydrocephalus omphalocele optic atrophy patent ductus arteriosus patent foramen ovale pathologic nystagmus placental insufficiency polyhydramnios popliteal pterygium syndrome ptosis pulmonary valve stenosis recurrent corneal erosion renal hypoplasia scoliosis senile degeneration of brain sensorineural hearing loss spina bifida occulta spondylolisthesis spontaneous ocular nystagmus syndactyly trichohepatoenteric syndrome 1 trichohepatoenteric syndrome umbilical hernia ventricular septal defect visual epilepsy
E9Q612	Receptor-type tyrosine-protein phosphatase O	Ptpro GLEPP1 PTPU2 Ptpn15	Mus musculus (house mouse)	11	6
P01127	Platelet-derived growth factor subunit B	PDGFB PDGF2 SIS	Homo sapiens (human)	3	6
Q8VI51	VPS10 domain-containing receptor SorCS3	Sorcs3	Mus musculus (house mouse)	7	6
Q86SJ2	Amphoterin-induced protein 2	AMIGO2 ALI1	Homo sapiens (human)	9	6
Q08481	Platelet endothelial cell adhesion molecule	Pecam1 Pecam Pecam-1	Mus musculus (house mouse)	7	6
P43356	Melanoma-associated antigen 2	MAGEA2 MAGEA2B MAGE2 MAGEA2 MAGEA2A	Homo sapiens (human)	1	6
Q9H2A7	C-X-C motif chemokine 16	CXCL16 SCYB16 SRPSOX	Homo sapiens (human)	14	6
Q9Z247	Peptidyl-prolyl cis-trans isomerase FKBP9	Fkbp9 Fkbp60 Fkbp63	Mus musculus (house mouse)	4	6
O60242	Adhesion G protein-coupled receptor B3	ADGRB3 BAI3 KIAA0550	Homo sapiens (human)	14	6
Q9EQU3	Toll-like receptor 9	Tlr9	Mus musculus (house mouse)	18	6
P10809	60 kDa heat shock protein, mitochondrial	HSPD1 HSP60	Homo sapiens (human)	5	6
Q8JZS4	Alkaline phosphatase	Alpl Akp2	Mus musculus (house mouse)	3	6

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