GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
Q9Y450	HBS1-like protein	HBS1L HBS1 KIAA1038	3	1
Q9BQE9	B-cell CLL/lymphoma 7 protein family member B	BCL7B	3	1
Q8NGY3	Olfactory receptor 6K3	OR6K3	3	1
Q8NGN1	Olfactory receptor 6T1	OR6T1	3	1
O15321	Transmembrane 9 superfamily member 1	TM9SF1	3	3
Q9Y6R9	Centrosomal protein CCDC61	CCDC61	3	1
Q8WW79	L-selectin	SELL	3	0
Q99996	A-kinase anchor protein 9	AKAP9 AKAP350 AKAP450 KIAA0803	3	3
A0A5P3YYA7	MHC Class I chain-related protein	MICA	3	0
Q9C0B2	Cilia- and flagella-associated protein 74	CFAP74 C1orf222 KIAA1751	3	1
Q9GZT5	Protein Wnt-10a	WNT10A	3	2
Q9BX73	TM2 domain-containing protein 2	TM2D2 BLP1	3	1
Q9Y5F6	Protocadherin gamma-C5	PCDHGC5	3	0
A0A142J239	Truncated MHC class I polypeptide-related sequence A (Fragment)	MICA	3	0
Q8IVF4	Dynein axonemal heavy chain 10	DNAH10 KIAA2017	3	3
Q5JXA9	Signal-regulatory protein beta-2	SIRPB2 PTPN1L PTPNS1L3	3	0
A4UGR9	Xin actin-binding repeat-containing protein 2	XIRP2 CMYA3	3	2
O94766	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3	B3GAT3	3	2	Hailey-Hailey disease Laron syndrome Larsen-like syndrome B3GAT3 type Marfan syndrome Rothmund-Thomson syndrome achondroplasia amblyopia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis 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 cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bicuspid aortic valve disease buphthalmos cancer cleft palate cleidocranial dysplasia clubfoot communicating hydrocephalus congenital heart disease craniosynostosis cutis laxa esotropia geroderma osteodysplasticum glaucoma hepatocellular carcinoma humeroradial synostosis hydrocephalus hydrophthalmos hyperopia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis isolated cleft palate juvenile glaucoma liver cancer liver carcinoma mal de Meleda mitral valve insufficiency mitral valve prolapse monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia obstructive hydrocephalus osteochondrodysplasia osteoporosis patent foramen ovale postinflammatory pulmonary fibrosis postural orthostatic tachycardia syndrome pulmonary fibrosis radioulnar synostosis refractive error restrictive dermopathy scoliosis senile degeneration of brain situs inversus strabismic amblyopia thoracic aortic aneurysm tuberous sclerosis
Q5HYM1	Uncharacterized protein DKFZp686O1553 (Fragment)	DKFZp686O1553	3	0
P32243	Homeobox protein OTX2	OTX2	3	1
P47972	Neuronal pentraxin-2	NPTX2	3	4
A0A7S7M539	MHC class I polypeptide-related sequence A	MICA	3	0
P42224	Signal transducer and activator of transcription 1-alpha/beta	STAT1	3	1
Q8NC51	SERPINE1 mRNA-binding protein 1	SERBP1 PAIRBP1	3	1
Q15061	WD repeat-containing protein 43	WDR43 KIAA0007 UTP5	3	3

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