GlyCosmos Portal

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q86YH2	Zinc finger protein 280B	ZNF280B SUHW2 ZNF279 ZNF632	0	1
Q86YF9	Cilium assembly protein DZIP1	DZIP1 DZIP DZIP2 KIAA0996	1	1
Q86YE8	Zinc finger protein 573	ZNF573	0	1
Q86YD5	Low-density lipoprotein receptor class A domain-containing protein 3	LDLRAD3 LRAD3	1	0
Q86YD3	Transmembrane protein 25	TMEM25	8	6
Q86YD1	Prostate tumor-overexpressed gene 1 protein	PTOV1 ACID2	0	1
Q86YC3	Transforming growth factor beta activator LRRC33	NRROS LRRC33	11	5
Q86YC2	Partner and localizer of BRCA2	PALB2 FANCN	1	1
Q86YB8	ERO1-like protein beta	ERO1B ERO1LB	4	12
Q86YA3	5'-3' DNA helicase ZGRF1	ZGRF1 C4orf21	1	1
Q86Y97	Histone-lysine N-methyltransferase KMT5C	KMT5C SUV420H2	0	1
Q86Y91	Kinesin-like protein KIF18B	KIF18B	1	2
Q86Y82	Syntaxin-12	STX12	0	1
Q86Y78	Ly6/PLAUR domain-containing protein 6	LYPD6	7	2	Gilles de la Tourette syndrome anxiety disorder generalized anxiety disorder phobic disorder
Q86Y56	Dynein axonemal assembly factor 5	DNAAF5 HEATR2	0	1
Q86Y39	NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 11	NDUFA11	0	1
Q86Y38	Xylosyltransferase 1	XYLT1 XT1	9	2	Barber-Say syndrome Bernard-Soulier syndrome Brooke-Spiegler syndrome Desbuquois dysplasia Duchenne muscular dystrophy Ehlers-Danlos syndrome Laron syndrome abdominal aortic aneurysm achondroplasia acne acute myeloid leukemia age related macular degeneration anaplastic astrocytoma angioid streaks anodontia arthritis arthropathy cerebral infarction cerebrovascular disease childhood cerebral astrocytoma chondrodysplasia punctata cleft palate cleidocranial dysplasia clubfoot congestive heart failure degeneration of macula and posterior pole degenerative disc disease diabetes mellitus diabetic ketoacidosis enophthalmos essential hypertension fibrillary astrocytoma gemistocytic astrocytoma glaucoma glomerulonephritis high grade glioma humeroradial synostosis hypertension hypertrichosis hypotrichosis intellectual disability intermittent claudication isolated cleft palate isolated growth hormone deficiency juvenile pilocytic astrocytoma keratosis follicularis kidney disease kidney failure learning disability macular degeneration malignant astrocytoma microcephaly mitral valve insufficiency mitral valve prolapse mitral valve stenosis mongolian spot mucopolysaccharidosis IV multiple epiphyseal dysplasia muscular dystrophy myopia nephritis nephrosis obsolete exophthalmos obsolete type 1 diabetes mellitus 9 orbital disease osteoarthritis osteochondrodysplasia osteogenesis imperfecta pilocytic astrocytoma placental insufficiency pleomorphic adenoma postural orthostatic tachycardia syndrome protoplasmic astrocytoma pseudoxanthoma elasticum pyoureter qualitative platelet defect radioulnar synostosis restrictive cardiomyopathy scoliosis subependymal giant cell astrocytoma substance abuse substance-related disorder tooth agenesis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ventricular septal defect
Q86Y37	CDK2-associated and cullin domain-containing protein 1	CACUL1 C10orf46 CAC1	4	1
Q86Y34	Adhesion G protein-coupled receptor G3	ADGRG3 GPR97 PGR26	4	0
Q86Y33	Cell division cycle protein 20 homolog B	CDC20B	1	1
Q86Y26	NUT family member 1	NUTM1 C15orf55 NUT	0	1
Q86Y25	Zinc finger protein 354C	ZNF354C KID3	0	1
Q86Y22	Collagen alpha-1(XXIII) chain	COL23A1	0	1
Q86XZ4	Spermatogenesis-associated serine-rich protein 2	SPATS2 SCR59 SPATA10	4	2
Q86XX4	Extracellular matrix organizing protein FRAS1	FRAS1 KIAA1500	22	30

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