GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
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Displaying entries **14176 - 14200** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P24928	DNA-directed RNA polymerase II subunit RPB1	POLR2A POLR2	Homo sapiens (human)	10	2
P26583	High mobility group protein B2	HMGB2 HMG2	Homo sapiens (human)	0	1
Q99536	Synaptic vesicle membrane protein VAT-1 homolog	VAT1	Homo sapiens (human)	0	1
O15218	G-protein coupled receptor 182	GPR182 ADMR	Homo sapiens (human)	2	0
P46976	Glycogenin-1	GYG1 GYG	Homo sapiens (human)	1	1	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Lafora disease cardiomyopathy catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia central nervous system origin vertigo coronary artery disease cystinuria diabetes mellitus disease of metabolism endomyocardial fibrosis familial periodic paralysis galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease XV glycogen storage disease hypertrophic cardiomyopathy myopathy sick sinus syndrome type 2 diabetes mellitus
Q6R2W3	SCAN domain-containing protein 3	SCAND3 Buster4 KIAA1925 ZBED9 ZNF305P2 ZNF452	Homo sapiens (human)	2	3
Q8N9B5	Junction-mediating and -regulatory protein	JMY	Homo sapiens (human)	1	1
K7P5R9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
A6NC98	Coiled-coil domain-containing protein 88B	CCDC88B BRLZ	Homo sapiens (human)	0	1
D6ML81	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q86Y38	Xylosyltransferase 1	XYLT1 XT1	Homo sapiens (human)	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
Q8NI35	InaD-like protein	PATJ CIPP INADL	Homo sapiens (human)	3	3
Q9Y385	Ubiquitin-conjugating enzyme E2 J1	UBE2J1 NCUBE1	Homo sapiens (human)	2	2
P60953	Cell division control protein 42 homolog	CDC42	Homo sapiens (human)	2	1
E2GJH5	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A0A0X7YL54	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P51957	Serine/threonine-protein kinase Nek4	NEK4 STK2	Homo sapiens (human)	1	1
F6IQL7	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P30050	Large ribosomal subunit protein uL11	RPL12	Homo sapiens (human)	0	1
Q96AP7	Endothelial cell-selective adhesion molecule	ESAM	Homo sapiens (human)	5	28
Q9H9B1	Histone-lysine N-methyltransferase EHMT1	EHMT1 EUHMTASE1 GLP KIAA1876 KMT1D	Homo sapiens (human)	1	5
O94874	E3 UFM1-protein ligase 1	UFL1 KIAA0776 MAXER NLBP RCAD	Homo sapiens (human)	0	1
Q6P9F7	Volume-regulated anion channel subunit LRRC8B	LRRC8B KIAA0231	Homo sapiens (human)	2	1
Q5JTB6	Placenta-specific protein 9	PLAC9	Homo sapiens (human)	1	1
Q9HBU6	Ethanolamine kinase 1	ETNK1 EKI1	Homo sapiens (human)	2	2	aggressive systemic mastocytosis atypical chronic myeloid leukemia, BCR-ABL1 negative cancer chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia disseminated eosinophilic collagen disease hypereosinophilic syndrome indolent systemic mastocytosis juvenile myelomonocytic leukemia mastocytosis myeloid leukemia obsolete subacute myeloid leukemia seminoma systemic mastocytosis testicular cancer testicular germ cell cancer testis seminoma

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