GlyCosmos Portal

Displaying entries **6601 - 6625** of **18496** in total

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
O76082	Organic cation/carnitine transporter 2	SLC22A5 OCTN2	3	6
O76083	High affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A	PDE9A	0	1
O76093	Fibroblast growth factor 18	FGF18	2	0
O76094	Signal recognition particle subunit SRP72	SRP72	4	3
O76095	Protein JTB	JTB	1	1
O76096	Cystatin-F	CST7	4	2
O76099	Olfactory receptor 7C1	OR7C1 OR7C4	2	1
O76100	Olfactory receptor 7A10	OR7A10	1	0
O78043	Leucocyte antigen B (Fragment)	HLA-B	1	0
O78075	MHC class I antigen (Fragment)	HLA-B	1	0
O78130	MHC class I antigen (Fragment)	HLA-B	1	0
O78137	MHC class I antigen (Fragment)	HLA-B	1	0
O78164	MHC class I antigen (Fragment)	HLA-C	1	0
O78170	HLA-B15IL protein (Fragment)	HLA-B*15IL	1	0
O94760	N(G),N(G)-dimethylarginine dimethylaminohydrolase 1	DDAH1 DDAH	0	1
O94761	ATP-dependent DNA helicase Q4	RECQL4 RECQ4	3	1
O94762	ATP-dependent DNA helicase Q5	RECQL5 RECQ5	2	1
O94763	Unconventional prefoldin RPB5 interactor 1	URI1 C19orf2 NNX3 PPP1R19 RMP URI	3	1
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
O94768	Serine/threonine-protein kinase 17B	STK17B DRAK2	0	1
O94769	Extracellular matrix protein 2	ECM2	6	21
O94772	Lymphocyte antigen 6H	LY6H	1	0
O94776	Metastasis-associated protein MTA2	MTA2 MTA1L1 PID	0	1
O94778	Aquaporin-8	AQP8	2	0
O94779	Contactin-5	CNTN5	9	0	Behcet's disease Hirschsprung's disease Parkinson's disease 2 anorexia nervosa atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar disorder communicating hydrocephalus congestive heart failure depressive disorder differentiated thyroid gland carcinoma essential hypertension gout hydrocephalus hypertension major depressive disorder melancholic depression neurotic disorder obsolete melancholia obstructive hydrocephalus primary biliary cholangitis schizophrenia senile degeneration of brain

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