GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **16151 - 16175** 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
Q86VP1	Tax1-binding protein 1	TAX1BP1 T6BP	Homo sapiens (human)	1	2
Q14204	Cytoplasmic dynein 1 heavy chain 1	DYNC1H1 DHC1 DNCH1 DNCL DNECL DYHC KIAA0325	Homo sapiens (human)	7	2
O95831	Apoptosis-inducing factor 1, mitochondrial	AIFM1 AIF PDCD8	Homo sapiens (human)	2	2
O43318	Mitogen-activated protein kinase kinase kinase 7	MAP3K7 TAK1	Homo sapiens (human)	4	2
P24928	DNA-directed RNA polymerase II subunit RPB1	POLR2A POLR2	Homo sapiens (human)	10	2
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
Q9Y385	Ubiquitin-conjugating enzyme E2 J1	UBE2J1 NCUBE1	Homo sapiens (human)	2	2
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
Q9HCF6	Transient receptor potential cation channel subfamily M member 3	TRPM3 KIAA1616 LTRPC3	Homo sapiens (human)	2	2
P78332	RNA-binding protein 6	RBM6 DEF3	Homo sapiens (human)	4	2
Q8IWG1	Dynein axonemal intermediate chain 3	DNAI3 WDR63	Homo sapiens (human)	1	2
P0DMV9	Heat shock 70 kDa protein 1B	HSPA1B HSP72	Homo sapiens (human)	3	2
Q9NR21	Protein mono-ADP-ribosyltransferase PARP11	PARP11 C12orf6	Homo sapiens (human)	1	2	microcephaly viral infectious disease
P57740	Nuclear pore complex protein Nup107	NUP107	Homo sapiens (human)	8	2
Q9UPN9	E3 ubiquitin-protein ligase TRIM33	TRIM33 KIAA1113 RFG7 TIF1G	Homo sapiens (human)	5	2
Q8N2E6	Prosalusin	TOR2A	Homo sapiens (human)	1	2
Q9NRJ7	Protocadherin beta-16	PCDHB16 KIAA1621 PCDH3X	Homo sapiens (human)	4	2
Q5JSZ5	Protein PRRC2B	PRRC2B BAT2L BAT2L1 KIAA0515	Homo sapiens (human)	9	2
A7MBM2	Protein dispatched homolog 2	DISP2 C15orf36 DISPB KIAA1742 LINC00594	Homo sapiens (human)	4	2
Q6P4F7	Rho GTPase-activating protein 11A	ARHGAP11A KIAA0013	Homo sapiens (human)	2	2
Q15847	Adipogenesis regulatory factor	ADIRF AFRO APM2 C10orf116	Homo sapiens (human)	2	2
Q5U623	Activating transcription factor 7-interacting protein 2	ATF7IP2 MCAF2	Homo sapiens (human)	1	2
P55198	Protein AF-17	MLLT6 AF17	Homo sapiens (human)	31	2
Q92597	Protein NDRG1	NDRG1 CAP43 DRG1 RTP	Homo sapiens (human)	3	2
O14545	TRAF-type zinc finger domain-containing protein 1	TRAFD1 FLN29	Homo sapiens (human)	3	2

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