GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
O00398	Putative P2Y purinoceptor 10	P2RY10	4	2
Q69YN4	Protein virilizer homolog	VIRMA KIAA1429	2	2
Q9UK61	Protein TASOR	TASOR C3orf63 FAM208A KIAA1105	6	2
P47897	Glutamine--tRNA ligase	QARS1 QARS	2	2
Q96A49	Synapse-associated protein 1	SYAP1	4	2
P05412	Transcription factor Jun	JUN	8	2
Q7Z403	Transmembrane channel-like protein 6	TMC6 EVER1 EVIN1	2	2
Q02750	Dual specificity mitogen-activated protein kinase kinase 1	MAP2K1 MEK1 PRKMK1	1	2
P35580	Myosin-10	MYH10	2	2
P54764	Ephrin type-A receptor 4	EPHA4 HEK8 SEK TYRO1	4	2
P49589	Cysteine--tRNA ligase, cytoplasmic	CARS1 CARS	2	2
Q13261	Interleukin-15 receptor subunit alpha	IL15RA	6	2
Q13356	RING-type E3 ubiquitin-protein ligase PPIL2	PPIL2	1	2
Q15363	Transmembrane emp24 domain-containing protein 2	TMED2 RNP24	2	2
Q14676	Mediator of DNA damage checkpoint protein 1	MDC1 KIAA0170 NFBD1	14	2
O15085	Rho guanine nucleotide exchange factor 11	ARHGEF11 KIAA0380	3	2
Q15813	Tubulin-specific chaperone E	TBCE	1	2
Q2TAY7	WD40 repeat-containing protein SMU1	SMU1	1	2
Q86VP1	Tax1-binding protein 1	TAX1BP1 T6BP	1	2
Q14204	Cytoplasmic dynein 1 heavy chain 1	DYNC1H1 DHC1 DNCH1 DNCL DNECL DYHC KIAA0325	7	2
O95831	Apoptosis-inducing factor 1, mitochondrial	AIFM1 AIF PDCD8	2	2
O43318	Mitogen-activated protein kinase kinase kinase 7	MAP3K7 TAK1	4	2
P24928	DNA-directed RNA polymerase II subunit RPB1	POLR2A POLR2	10	2
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
Q9Y385	Ubiquitin-conjugating enzyme E2 J1	UBE2J1 NCUBE1	2	2

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