GlyCosmos Portal

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9H7D7	WD repeat-containing protein 26	WDR26 CDW2 MIP2	0	1
Q9H7D0	Dedicator of cytokinesis protein 5	DOCK5	4	3
Q9H7B4	Histone-lysine N-methyltransferase SMYD3	SMYD3 ZMYND1 ZNFN3A1	0	1
Q9H7B2	Ribosome production factor 2 homolog	RPF2 BXDC1	0	1
Q9H792	Inactive tyrosine-protein kinase PEAK1	PEAK1 KIAA2002	7	12
Q9H788	SH2 domain-containing protein 4A	SH2D4A PPP1R38 SH2A	1	1
Q9H773	dCTP pyrophosphatase 1	DCTPP1 XTP3TPA	1	1
Q9H772	Gremlin-2	GREM2 CKTSF1B2 DAND3 PRDC	2	0
Q9H765	Ankyrin repeat and SOCS box protein 8	ASB8	0	1
Q9H756	Leucine-rich repeat-containing protein 19	LRRC19	10	0
Q9H741	SREBP regulating gene protein	SPRING1 C12orf49 SPRING	8	2
Q9H720	PGAP2-interacting protein	CWH43 PGAP2IP	1	0
Q9H707	Zinc finger protein 552	ZNF552	1	1
Q9H6Z4	Ran-binding protein 3	RANBP3	1	2
Q9H6Y7	E3 ubiquitin-protein ligase RNF167	RNF167 RING105	2	0
Q9H6Y2	WD repeat-containing protein 55	WDR55	0	1
Q9H6X2	Anthrax toxin receptor 1	ANTXR1 ATR TEM8	3	2
Q9H6U8	Alpha-1,2-mannosyltransferase ALG9	ALG9 DIBD1	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	0	1
Q9H6T3	RNA polymerase II-associated protein 3	RPAP3	0	1
Q9H6S3	Epidermal growth factor receptor kinase substrate 8-like protein 2	EPS8L2 EPS8R2	1	1
Q9H6S0	3'-5' RNA helicase YTHDC2	YTHDC2	2	2
Q9H6R7	WD repeat and coiled-coil-containing protein	WDCP C2orf44	1	1
Q9H6R4	Nucleolar protein 6	NOL6	0	1
Q9H6R3	Acyl-CoA synthetase short-chain family member 3, mitochondrial	ACSS3	1	1	cancer embryoma stomach cancer stomach carcinoma

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