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 **726 - 750** 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
P15260	Interferon gamma receptor 1	IFNGR1	Homo sapiens (human)	5	13
P35527	Keratin, type I cytoskeletal 9	KRT9	Homo sapiens (human)	3	13
Q14643	Inositol 1,4,5-trisphosphate-gated calcium channel ITPR1	ITPR1 INSP3R1	Homo sapiens (human)	6	13
P17927	Complement receptor type 1	CR1 C3BR	Homo sapiens (human)	21	13
Q96BZ4	5'-3' exonuclease PLD4	PLD4 C14orf175	Homo sapiens (human)	10	13	Usher syndrome type 2 Usher syndrome type 3 Usher syndrome colon cancer colon carcinoma colonic benign neoplasm colorectal cancer hepatitis large intestine cancer retinitis pigmentosa-deafness syndrome rheumatoid arthritis scleroderma systemic scleroderma
Q9BVK6	Transmembrane emp24 domain-containing protein 9	TMED9 GP25L2	Homo sapiens (human)	1	13	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia Unverricht-Lundborg syndrome adult T-cell leukemia/lymphoma alternating hemiplegia of childhood amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease autonomic neuropathy autosomal recessive distal hereditary motor neuronopathy 1 cancer central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer dentatorubral-pallidoluysian atrophy early myoclonic encephalopathy epilepsy frontotemporal dementia generalized anxiety disorder large intestine cancer lateral sclerosis malaria motor neuron disease nervous system disease neurodegenerative disease nonpapillary renal cell carcinoma obsolete T-cell lymphoblastic leukemia/lymphoma optic atrophy 1 optic atrophy papillary renal cell carcinoma phototoxic dermatitis progressive muscular atrophy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma status epilepticus tuberculosis visual epilepsy
Q02223	Tumor necrosis factor receptor superfamily member 17	TNFRSF17 BCM BCMA	Homo sapiens (human)	1	13
Q9UQC9	Calcium-activated chloride channel regulator 2	CLCA2 CACC3	Homo sapiens (human)	10	13
P17181	Interferon alpha/beta receptor 1	IFNAR1 IFNAR	Homo sapiens (human)	13	13
P08582	Melanotransferrin	MELTF MAP97 MFI2	Homo sapiens (human)	3	13	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease MHC class II deficiency Pick's disease Reye syndrome Roberts syndrome Zollinger-Ellison syndrome adenosine deaminase deficiency angiomyolipoma astigmatism bone osteosarcoma cancer carcinoma central nervous system cancer cerebral degeneration cerebral primitive neuroectodermal tumor cervical cancer cervix carcinoma childhood osteosarcoma colorectal cancer colorectal carcinoma dysplastic nevus syndrome embryoma gliosarcoma high grade glioma hyperinsulinism large intestine cancer lung adenocarcinoma lung cancer medulloblastoma medulloepithelioma melanoma melanotic neuroectodermal tumor mixed glioma neuroectodermal tumor obsolete SC phocomelia syndrome obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered osteosarcoma polycystic ovary syndrome sarcomatoid carcinoma severe combined immunodeficiency skin melanoma stomach cancer stomach carcinoma supratentorial primitive neuroectodermal tumor
Q9GZX9	Twisted gastrulation protein homolog 1	TWSG1 TSG	Homo sapiens (human)	3	13
Q9ULF5	Zinc transporter ZIP10	SLC39A10 KIAA1265 ZIP10	Homo sapiens (human)	14	13
P06028	Glycophorin-B	GYPB GPB	Homo sapiens (human)	4	13
Q5T2D2	Trem-like transcript 2 protein	TREML2 C6orf76 TLT2	Homo sapiens (human)	1	13
O60566	Mitotic checkpoint serine/threonine-protein kinase BUB1 beta	BUB1B BUBR1 MAD3L SSK1	Homo sapiens (human)	4	13
Q06418	Tyrosine-protein kinase receptor TYRO3	TYRO3 BYK DTK RSE SKY TIF	Homo sapiens (human)	7	13
P05981	Serine protease hepsin	HPN TMPRSS1	Homo sapiens (human)	1	13
O00462	Beta-mannosidase	MANBA MANB1	Homo sapiens (human)	8	13	Fabry disease allergic asthma allergic disease alternating hemiplegia of childhood angiokeratoma ascending cholangitis asthma attention deficit hyperactivity disorder autonomic neuropathy beta-mannosidosis central nervous system disease cholangitis chronic kidney disease chylomicron retention disease colorectal cancer colorectal carcinoma complement deficiency congenital nystagmus dissociated nystagmus epilepsy intellectual disability intrinsic asthma large intestine cancer learning disability lipid storage disease lysosomal storage disease multiple sclerosis nervous system disease obsolete constipation pathologic nystagmus primary biliary cholangitis primary sclerosing cholangitis sarcoidosis sclerosing cholangitis sensorineural hearing loss speech disorder spontaneous ocular nystagmus suppurative cholangitis uveoparotid fever visual epilepsy
O94905	Erlin-2	ERLIN2 C8orf2 SPFH2	Homo sapiens (human)	7	13
Q16585	Beta-sarcoglycan	SGCB	Homo sapiens (human)	4	13
Q92791	Endoplasmic reticulum protein SC65	P3H4 LEPREL4 NOL55 SC65	Homo sapiens (human)	3	13
P27701	CD82 antigen	CD82 KAI1 SAR2 ST6 TSPAN27	Homo sapiens (human)	5	13
P07093	Glia-derived nexin	SERPINE2 PI7 PN1	Homo sapiens (human)	5	12
Q96DT5	Dynein axonemal heavy chain 11	DNAH11	Homo sapiens (human)	2	12
P42702	Leukemia inhibitory factor receptor	LIFR	Homo sapiens (human)	22	12

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