GlyCosmos Portal

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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 **9601 - 9625** 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
Q9H788	SH2 domain-containing protein 4A	SH2D4A PPP1R38 SH2A	Homo sapiens (human)	1	1
Q9H773	dCTP pyrophosphatase 1	DCTPP1 XTP3TPA	Homo sapiens (human)	1	1
Q9H772	Gremlin-2	GREM2 CKTSF1B2 DAND3 PRDC	Homo sapiens (human)	2	0
Q9H765	Ankyrin repeat and SOCS box protein 8	ASB8	Homo sapiens (human)	0	1
Q9H756	Leucine-rich repeat-containing protein 19	LRRC19	Homo sapiens (human)	10	0
Q9H741	SREBP regulating gene protein	SPRING1 C12orf49 SPRING	Homo sapiens (human)	8	2
Q9H720	PGAP2-interacting protein	CWH43 PGAP2IP	Homo sapiens (human)	1	0
Q9H707	Zinc finger protein 552	ZNF552	Homo sapiens (human)	1	1
Q9H6Z4	Ran-binding protein 3	RANBP3	Homo sapiens (human)	1	2
Q9H6Y7	E3 ubiquitin-protein ligase RNF167	RNF167 RING105	Homo sapiens (human)	2	0
Q9H6Y2	WD repeat-containing protein 55	WDR55	Homo sapiens (human)	0	1
Q9H6X2	Anthrax toxin receptor 1	ANTXR1 ATR TEM8	Homo sapiens (human)	3	2
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
Q9H6U6	BCAS3 microtubule associated cell migration factor	BCAS3	Homo sapiens (human)	0	1
Q9H6T3	RNA polymerase II-associated protein 3	RPAP3	Homo sapiens (human)	0	1
Q9H6S3	Epidermal growth factor receptor kinase substrate 8-like protein 2	EPS8L2 EPS8R2	Homo sapiens (human)	1	1
Q9H6S0	3'-5' RNA helicase YTHDC2	YTHDC2	Homo sapiens (human)	2	2
Q9H6R7	WD repeat and coiled-coil-containing protein	WDCP C2orf44	Homo sapiens (human)	1	1
Q9H6R4	Nucleolar protein 6	NOL6	Homo sapiens (human)	0	1
Q9H6R3	Acyl-CoA synthetase short-chain family member 3, mitochondrial	ACSS3	Homo sapiens (human)	1	1	cancer embryoma stomach cancer stomach carcinoma
Q9H6Q4	Cytosolic iron-sulfur assembly component 3	CIAO3 NARFL PRN	Homo sapiens (human)	2	1
Q9H6N6	Putative uncharacterized protein MYH16	MYH16 MYH5	Homo sapiens (human)	0	1
Q9H6L5	Reticulophagy regulator 1	RETREG1 FAM134B JK1	Homo sapiens (human)	0	1
Q9H6L2	Transmembrane protein 231	TMEM231	Homo sapiens (human)	5	6
Q9H6K5	Proline-rich protein 36	PRR36	Homo sapiens (human)	0	1

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