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 **16101 - 16125** 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
Q15691	Microtubule-associated protein RP/EB family member 1	MAPRE1	Homo sapiens (human)	5	1
P36507	Dual specificity mitogen-activated protein kinase kinase 2	MAP2K2 MEK2 MKK2 PRKMK2	Homo sapiens (human)	5	1
Q7Z7B0	Filamin-A-interacting protein 1	FILIP1 KIAA1275	Homo sapiens (human)	5	1
C9JH25	Proline-rich transmembrane protein 4	PRRT4	Homo sapiens (human)	5	2
Q9Y2A9	N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 3	B3GNT3 B3GALT8 TMEM3	Homo sapiens (human)	5	0	cancer cervical adenocarcinoma cervical cancer cervix carcinoma common wart embryoma influenza lung cancer lung non-small cell carcinoma neuroblastoma
P78539	Sushi repeat-containing protein SRPX	SRPX ETX1	Homo sapiens (human)	5	1
P48723	Heat shock 70 kDa protein 13	HSPA13 STCH	Homo sapiens (human)	5	11
Q9NZQ7	Programmed cell death 1 ligand 1	CD274 B7H1 PDCD1L1 PDCD1LG1 PDL1	Homo sapiens (human)	5	1
Q8IW00	V-set and transmembrane domain-containing protein 4	VSTM4 C10orf72	Homo sapiens (human)	5	3
P53396	ATP-citrate synthase	ACLY	Homo sapiens (human)	5	2	Behcet's disease Zollinger-Ellison syndrome abdominal aortic aneurysm acute myeloid leukemia adult oligodendroglioma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiac arrest cardiovascular system disease childhood oligodendroglioma childhood osteosarcoma chromophobe renal cell carcinoma chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease diabetes mellitus disease of metabolism embryoma enthesopathy exostosis familial hyperlipidemia heart disease hepatocellular carcinoma high grade glioma hyperinsulinism inclusion body myositis kwashiorkor large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma marasmus mast-cell leukemia mastocytosis mixed oligodendroglioma-astrocytoma neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis nonpapillary renal cell carcinoma nutrition disease obesity oligodendroglioma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma papillary renal cell carcinoma periarthritis polycystic kidney disease 3 prostate cancer prostate carcinoma protein-energy malnutrition renal carcinoma renal cell carcinoma renal osteodystrophy sarcomatoid renal cell carcinoma septic arthritis squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma synovitis tendinitis tenosynovitis tongue squamous cell carcinoma trigeminal neuralgia type 2 diabetes mellitus
Q08334	Interleukin-10 receptor subunit beta	IL10RB CRFB4 D21S58 D21S66	Homo sapiens (human)	5	1
Q9Y5E5	Protocadherin beta-4	PCDHB4	Homo sapiens (human)	5	1
P0DN25	C1GALT1-specific chaperone 1-like protein	C1GALT1C1L	Homo sapiens (human)	5	2
P54198	Protein HIRA	HIRA DGCR1 HIR TUPLE1	Homo sapiens (human)	5	1
Q969N2	GPI transamidase component PIG-T	PIGT	Homo sapiens (human)	5	16	Marfan syndrome angioedema blindness brain disease breast cancer breast carcinoma calcinosis calcium metabolism disease cerebral degeneration congenital nystagmus craniosynostosis cystic kidney disease dermatographia diarrhea dissociated nystagmus epilepsy esotropia fibromyalgia hemolytic anemia hypercalcemia hyperopia hypertropia hypophosphatasia mechanical strabismus monocular esotropia multiple congenital anomalies-hypotonia-seizures syndrome 3 myositis nephrocalcinosis non-congenital cyst of kidney ophthalmoplegia osteoporosis paroxysmal nocturnal hemoglobinuria patent ductus arteriosus pathologic nystagmus phosphorus metabolism disease restrictive cardiomyopathy scoliosis situs inversus spontaneous ocular nystagmus strabismus tuberous sclerosis urticaria visual epilepsy
Q13769	THO complex subunit 5 homolog	THOC5 C22orf19 KIAA0983	Homo sapiens (human)	5	1
Q8TEB7	E3 ubiquitin-protein ligase RNF128	RNF128	Homo sapiens (human)	5	2
Q8NDV1	Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	ST6GALNAC3 SIAT7C	Homo sapiens (human)	5	1	diabetes mellitus gestational diabetes idiopathic scoliosis prostate cancer prostate carcinoma type 2 diabetes mellitus
Q8TDQ0	Hepatitis A virus cellular receptor 2	HAVCR2 TIM3 TIMD3	Homo sapiens (human)	5	7
Q8NFP9	Neurobeachin	NBEA BCL8B KIAA1544 LYST2	Homo sapiens (human)	5	5
Q9BRQ5	Protein orai-3	ORAI3 TMEM142C	Homo sapiens (human)	5	2
Q9Y512	Sorting and assembly machinery component 50 homolog	SAMM50 SAM50	Homo sapiens (human)	5	1
O95727	Cytotoxic and regulatory T-cell molecule	CRTAM	Homo sapiens (human)	5	2
P03986	T cell receptor gamma constant 2	TRGC2 TCRGC2	Homo sapiens (human)	5	0
Q9Y5Z0	Beta-secretase 2	BACE2 AEPLC ALP56 ASP21	Homo sapiens (human)	5	5

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