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 **13926 - 13950** 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
P61813	C-C chemokine receptor type 5	CCR5 CMKBR5	Macaca mulatta (Rhesus monkey)	4	0
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
Q9IB86	Calcitonin gene-related peptide type 1 receptor	calcrl cgrpr	Paralichthys olivaceus (Japanese flounder)	4	0
F7A1B4	Endoglin	Eng	Mus musculus (house mouse)	4	0
Q9LSG3	Galacturonosyltransferase 8	GAUT8 QUA1	Arabidopsis thaliana (thale cress)	4	0
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
Q95R48	Organic cation transporter-like protein	Orct2	Drosophila melanogaster (fruit fly)	4	0
Q00716	Protein A56	HA	Raccoonpox virus	4	0
Q9HCE3	Zinc finger protein 532	ZNF532 KIAA1629	Homo sapiens (human)	4	1
P25357	Probable DNA-binding protein SNT1	SNT1	Saccharomyces cerevisiae S288C	4	1
P61642	Alpha-N-acetylneuraminide alpha-2,8-sialyltransferase	ST8SIA1 SIAT8A	Pan troglodytes (chimpanzee)	4	0
P58876	Histone H2B type 1-D	H2BC5 H2BFB HIRIP2 HIST1H2BD	Homo sapiens (human)	4	1
Q23490	Peroxidase mlt-7	mlt-7	Caenorhabditis elegans	4	0
O62698	Prostaglandin G/H synthase 2	PTGS2 COX2	Bos taurus (cattle)	4	0
B3IUA8	Flocculin	Lg-FLO1	Saccharomyces pastorianus	4	0
P46504	Uncharacterized protein F23F12.8	F23F12.8	Caenorhabditis elegans	4	0
P0DTJ0	Envelopment polyprotein	GP	Orthohantavirus nigrorivense	4	0
Q9FFE8	Wax ester synthase/diacylglycerol acyltransferase 8	WSD8	Arabidopsis thaliana (thale cress)	4	0
Q54WM0	Transmembrane protein 184 homolog DDB_G0279555	tmem184C	Dictyostelium discoideum	4	0
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
O88904	Homeodomain-interacting protein kinase 1	Hipk1 Kiaa0630 Myak Nbak2	Mus musculus (house mouse)	4	2
Q70E73	Ras-associated and pleckstrin homology domains-containing protein 1	RAPH1 ALS2CR18 ALS2CR9 KIAA1681 LPD PREL2 RMO1	Homo sapiens (human)	4	1
Q80V42	Carboxypeptidase M	Cpm	Mus musculus (house mouse)	4	14
Q08509	Epidermal growth factor receptor kinase substrate 8	Eps8	Mus musculus (house mouse)	4	4

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