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 **4601 - 4625** 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
O43286	Beta-1,4-galactosyltransferase 5	B4GALT5	Homo sapiens (human)	10	2	cancer central nervous system cancer colorectal cancer colorectal carcinoma diabetes mellitus diabetic ketoacidosis embryoma gliosarcoma high grade glioma large intestine cancer mixed glioma obesity type 2 diabetes mellitus
Q13422	DNA-binding protein Ikaros	IKZF1 IK1 IKAROS LYF1 ZNFN1A1	Homo sapiens (human)	3	2
Q969U6	F-box/WD repeat-containing protein 5	FBXW5 FBW5	Homo sapiens (human)	1	2
Q96JF0	Beta-galactoside alpha-2,6-sialyltransferase 2	ST6GAL2 KIAA1877 SIAT2	Homo sapiens (human)	8	2	breast cancer esophageal cancer esophageal carcinoma thyroid gland follicular carcinoma
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
Q9HBD1	Roquin-2	RC3H2 MNAB RNF164	Homo sapiens (human)	25	2
P61106	Ras-related protein Rab-14	RAB14	Homo sapiens (human)	1	2
P18858	DNA ligase 1	LIG1	Homo sapiens (human)	1	2
O00566	U3 small nucleolar ribonucleoprotein protein MPP10	MPHOSPH10 MPP10	Homo sapiens (human)	4	2
Q8WX77	Insulin-like growth factor-binding protein-like 1	IGFBPL1 IGFBPRP4	Homo sapiens (human)	2	2
O75113	NEDD4-binding protein 1	N4BP1 KIAA0615	Homo sapiens (human)	8	2
P15923	Transcription factor E2-alpha	TCF3 BHLHB21 E2A ITF1	Homo sapiens (human)	4	2
O70551	SRSF protein kinase 1	Srpk1	Mus musculus (house mouse)	2	2
Q8TDM6	Disks large homolog 5	DLG5 KIAA0583 PDLG	Homo sapiens (human)	9	2
P42128	Forkhead box protein K1	Foxk1 Mnf	Mus musculus (house mouse)	10	2
P61981	14-3-3 protein gamma	YWHAG	Homo sapiens (human)	1	2
Q9UBK8	Methionine synthase reductase	MTRR	Homo sapiens (human)	1	2
Q96ST3	Paired amphipathic helix protein Sin3a	SIN3A	Homo sapiens (human)	10	2
O75170	Serine/threonine-protein phosphatase 6 regulatory subunit 2	PPP6R2 KIAA0685 PP6R2 SAPS2	Homo sapiens (human)	7	2
O14763	Tumor necrosis factor receptor superfamily member 10B	TNFRSF10B DR5 KILLER TRAILR2 TRICK2 ZTNFR9	Homo sapiens (human)	2	2
Q64105	Sepiapterin reductase	Spr	Mus musculus (house mouse)	1	2
Q9DBC3	Cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 1	Cmtr1 Ftsjd2 Kiaa0082	Mus musculus (house mouse)	1	2
Q62108	Disks large homolog 4	Dlg4 Dlgh4 Psd95	Mus musculus (house mouse)	1	2
O35710	Nocturnin	Noct Ccr4 Ccrn4l Noc	Mus musculus (house mouse)	1	2
P09405	Nucleolin	Ncl Nuc	Mus musculus (house mouse)	1	2

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