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 **17751 - 17775** 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
O95998	Interleukin-18-binding protein	IL18BP	Homo sapiens (human)	7	13
Q9HCE0	Ectopic P granules protein 5 homolog	EPG5 KIAA1632	Homo sapiens (human)	1	13
O94813	Slit homolog 2 protein	SLIT2 SLIL3	Homo sapiens (human)	12	13
P46531	Neurogenic locus notch homolog protein 1	NOTCH1 TAN1	Homo sapiens (human)	57	13
Q6P4Q7	Metal transporter CNNM4	CNNM4 ACDP4 KIAA1592	Homo sapiens (human)	5	13
Q96G97	Seipin	BSCL2	Homo sapiens (human)	2	13
P23280	Carbonic anhydrase 6	CA6	Homo sapiens (human)	3	13
Q96AE7	Tetratricopeptide repeat protein 17	TTC17	Homo sapiens (human)	7	13
P07307	Asialoglycoprotein receptor 2	ASGR2 CLEC4H2	Homo sapiens (human)	3	13
P54753	Ephrin type-B receptor 3	EPHB3 ETK2 HEK2 TYRO6	Homo sapiens (human)	3	13
Q6UXH9	Inactive serine protease PAMR1	PAMR1 RAMP	Homo sapiens (human)	9	13
Q4G148	Glucoside xylosyltransferase 1	GXYLT1 GLT8D3	Homo sapiens (human)	6	13
O95490	Adhesion G protein-coupled receptor L2	ADGRL2 KIAA0786 LEC1 LPHH1 LPHN2	Homo sapiens (human)	17	13
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

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