GlyCosmos Portal

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The O-GlcNAc Database	June 3, 2024
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Displaying entries **111001 - 111025** 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
Q9SFC4	O-fucosyltransferase 24	OFUT24	Arabidopsis thaliana (thale cress)	4	0
P35659	Protein DEK	DEK	Homo sapiens (human)	4	1
Q8R2E9	ERO1-like protein beta	Ero1b Ero1lb	Mus musculus (house mouse)	4	5
Q9DAV2	Platelet-derived growth factor receptor-like protein	Flt1	Mus musculus (house mouse)	4	0
Q3UCC3	Interferon alpha/beta receptor 2	Ifnar2	Mus musculus (house mouse)	4	0
B8XGQ8	Subtilisin-like protease 5	SUB5	Trichophyton tonsurans	4	0
Q5DRD2	Protocadherin beta-2	PCDHB2	Pan troglodytes (chimpanzee)	4	0
P11841	Kappa-casein	CSN3 CSN10 CSNK	Sus scrofa (pig)	4	0
Q96S37	Solute carrier family 22 member 12	SLC22A12 OATL4 URAT1	Homo sapiens (human)	4	1
E9PX01	Glutamate receptor, ionotropic, AMPA4 (alpha 4)	Gria4	Mus musculus (house mouse)	4	0
Q9FWA4	Probable galacturonosyltransferase 9	GAUT9	Arabidopsis thaliana (thale cress)	4	0
P17945	Hepatocyte growth factor	Hgf	Rattus norvegicus (Norway rat)	4	0
F4K6F1	Xyloglucan galactosyltransferase XLT2	XLT2 GT18	Arabidopsis thaliana (thale cress)	4	0
A0A2K5M6L7	N-acylethanolamine-hydrolyzing acid amidase	NAAA	Cercocebus atys (sooty mangabey)	4	0
P47937	Neuromedin-K receptor	Tacr3 Tac3r	Mus musculus (house mouse)	4	0
Q3UWN7	V-type proton ATPase subunit S1 (Fragment)	Atp6ap1	Mus musculus (house mouse)	4	0
P29122	Proprotein convertase subtilisin/kexin type 6	PCSK6 PACE4	Homo sapiens (human)	4	2
Q9QUT0	Ammonium transporter Rh type A	Rhag Rh50	Mus musculus (house mouse)	4	0
Q9ZR79	L-type lectin-domain containing receptor kinase V.7	LECRK57 LECRKA3	Arabidopsis thaliana (thale cress)	4	0
P0DTN6	Putative amino acid/polyamine transporter MPH_07630_2	MPH_07630_2	Macrophomina phaseolina MS6	4	0
Q5S248	Transmembrane protease serine 11E	Tmprss11e Desc1	Mus musculus (house mouse)	4	0
E4UYL6	Probable dipeptidyl-aminopeptidase B	DAPB	Nannizzia gypsea CBS 118893	4	0
Q9H6U8	Alpha-1,2-mannosyltransferase ALG9	ALG9 DIBD1	Homo sapiens (human)	4	2	Gilles de la Tourette syndrome Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome autosomal dominant polycystic kidney disease cardiovascular system disease congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital heart disease congestive heart failure craniosynostosis cystic kidney disease cystinuria enophthalmos epilepsy esotropia galactokinase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease heart disease heart septal defect hemopericardium intellectual disability learning disability microcephaly monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia neuroendocrine carcinoma neuroendocrine tumor obsolete exophthalmos orbital disease osteochondrodysplasia pericardial effusion polycystic kidney disease 1 polycystic liver disease psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder situs inversus tuberous sclerosis visual epilepsy
P16157	Ankyrin-1	ANK1 ANK	Homo sapiens (human)	4	1
A0A0C4DGL8	Haptoglobin	HP	Homo sapiens (human)	4	0

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