GlyCosmos Portal

Displaying entries **13426 - 13450** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
P01138	Beta-nerve growth factor	NGF NGFB	5	1
P41225	Transcription factor SOX-3	SOX3	0	1
Q9Y394	Dehydrogenase/reductase SDR family member 7	DHRS7 DHRS7A RETSDR4 SDR34C1	0	1
P17987	T-complex protein 1 subunit alpha	TCP1 CCT1 CCTA	0	1
Q8NCN4	E3 ubiquitin-protein ligase RNF169	RNF169 KIAA1991	0	1
Q96QK1	Vacuolar protein sorting-associated protein 35	VPS35 MEM3	0	1
Q6P6B1	Glutamate-rich protein 5	ERICH5 C8orf47	0	1
P48507	Glutamate--cysteine ligase regulatory subunit	GCLM GLCLR	0	1
Q8IVD9	NudC domain-containing protein 3	NUDCD3 KIAA1068	0	1
Q96SI9	Spermatid perinuclear RNA-binding protein	STRBP SPNR	0	1
Q53H96	Pyrroline-5-carboxylate reductase 3	PYCR3 PYCRL	0	1
Q14055	Collagen alpha-2(IX) chain	COL9A2	2	1	Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Dowling-Degos disease Ehlers-Danlos syndrome Laron syndrome Laurin-Sandrow syndrome Osgood-Schlatter's disease Stickler syndrome achondroplasia acrodermatitis adult medulloblastoma allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia alternating hemiplegia of childhood amblyopia arthritis arthropathy asthma astigmatism atrial fibrillation autonomic neuropathy bone disease bone osteosarcoma cancer cardiovascular system disease cartilage disease cataract central nervous system cancer central nervous system disease childhood medulloblastoma childhood osteosarcoma chondrodysplasia punctata chronic kidney disease cleft palate collagen disease connective tissue disease degenerative disc disease depressive disorder dermatitis diabetes mellitus diastrophic dysplasia disease of metabolism dysplastic nevus syndrome dysthymic disorder epithelioid sarcoma essential hypertension eye disease familial hypercholesterolemia familial mediterranean fever familial periodic paralysis gliosarcoma granuloma annulare heart disease hemoglobin H disease high grade glioma hypertension intrinsic asthma isolated cleft palate major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma mevalonic aciduria mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia 2 multiple epiphyseal dysplasia myopathy myopia nervous system disease neurotic disorder obsolete melancholia osteoarthritis osteochondritis dissecans osteochondrodysplasia osteochondrosis osteogenesis imperfecta osteosarcoma pancreatic ductal adenocarcinoma pseudoachondroplasia reticulate acropigmentation of Kitamura retinal detachment rheumatoid arthritis sarcoma sensorineural hearing loss spinal stenosis spindle cell sarcoma strabismic amblyopia thalassemia thoracic aortic aneurysm type 2 diabetes mellitus
Q9BS31	Zinc finger protein 649	ZNF649	1	1
Q9H4R4	Putative nuclear receptor corepressor 1-like protein NCOR1P1	NCOR1P1 C20orf191	0	1
Q9NY37	Acid-sensing ion channel 5	ASIC5 ACCN5 HINAC	2	1
P62241	Small ribosomal subunit protein eS8	RPS8	0	1
Q86SQ3	Putative adhesion G protein-coupled receptor E4P	ADGRE4P EMR4 EMR4P GPR127 PGR16	4	1
Q9HAV5	Tumor necrosis factor receptor superfamily member 27	EDA2R TNFRSF27 XEDAR	1	1
Q9Y2K2	Serine/threonine-protein kinase SIK3	SIK3 KIAA0999 QSK	1	1
Q99714	3-hydroxyacyl-CoA dehydrogenase type-2	HSD17B10 ERAB HADH2 MRPP2 SCHAD SDR5C1 XH98G2	1	1
Q9NZT2	Opioid growth factor receptor	OGFR	0	1
P02489	Alpha-crystallin A chain	CRYAA CRYA1 HSPB4	1	1
Q9H7B4	Histone-lysine N-methyltransferase SMYD3	SMYD3 ZMYND1 ZNFN3A1	0	1
P60842	Eukaryotic initiation factor 4A-I	EIF4A1 DDX2A EIF4A	2	1
Q9HAS0	Protein Njmu-R1	C17orf75	0	1

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