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 **4076 - 4100** 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
O15294	UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit	OGT	Homo sapiens (human)	13	1	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 Pick's disease Reye syndrome Zollinger-Ellison syndrome amblyopia aortic valve disease 2 aortic valve stenosis autoimmune hepatitis breast cancer breast carcinoma cancer cardiovascular system disease cerebral degeneration chromophobe renal cell carcinoma chronic ulcer of skin clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma congenital nystagmus congestive heart failure cryptorchidism diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diffuse large B-cell lymphoma dissociated nystagmus embryoma heart disease hepatitis C hepatocellular carcinoma hyperinsulinism hypospadias intellectual disability large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer learning disability liver cancer liver carcinoma liver cirrhosis microcephaly microphthalmia myoepithelioma neurodegenerative disease non-syndromic X-linked intellectual disability 106 nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma pathologic nystagmus renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma spontaneous ocular nystagmus steatotic liver disease stomach cancer stomach carcinoma strabismic amblyopia tauopathy type 2 diabetes mellitus
Q9H4L7	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1	SMARCAD1 KIAA1122	Homo sapiens (human)	0	1
O60231	Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16	DHX16 DBP2 DDX16 KIAA0577 PRP2	Homo sapiens (human)	0	1
P56645	Period circadian protein homolog 3	PER3	Homo sapiens (human)	1	1
Q9NPI1	Bromodomain-containing protein 7	BRD7 BP75 CELTIX1	Homo sapiens (human)	0	1
Q6WRX3	Protein zyg-11 homolog A	ZYG11A ZYG11	Homo sapiens (human)	1	1
Q9BTW9	Tubulin-specific chaperone D	TBCD KIAA0988 SSD1 TFCD	Homo sapiens (human)	2	1
P57053	Histone H2B type F-S	H2BC12L H2BFS H2BS1	Homo sapiens (human)	1	1
Q9UJ70	N-acetyl-D-glucosamine kinase	NAGK	Homo sapiens (human)	0	1	prostate cancer prostate carcinoma
P41161	ETS translocation variant 5	ETV5 ERM	Homo sapiens (human)	0	1
Q8WVM0	Dimethyladenosine transferase 1, mitochondrial	TFB1M	Homo sapiens (human)	0	1
Q9UM00	Calcium load-activated calcium channel	TMCO1 TMCC4	Homo sapiens (human)	2	1
O75955	Flotillin-1	FLOT1	Homo sapiens (human)	0	1
Q9UNW9	RNA-binding protein Nova-2	NOVA2 ANOVA NOVA3	Homo sapiens (human)	0	1
Q14240	Eukaryotic initiation factor 4A-II	EIF4A2 DDX2B EIF4F	Homo sapiens (human)	0	1
Q6EMB2	Tubulin polyglutamylase TTLL5	TTLL5 KIAA0998 STAMP	Homo sapiens (human)	1	1
Q02790	Peptidyl-prolyl cis-trans isomerase FKBP4	FKBP4 FKBP52	Homo sapiens (human)	3	1
O75586	Mediator of RNA polymerase II transcription subunit 6	MED6 ARC33	Homo sapiens (human)	0	1
Q01650	Large neutral amino acids transporter small subunit 1	SLC7A5 CD98LC LAT1 MPE16	Homo sapiens (human)	0	1
Q8TE49	OTU domain-containing protein 7A	OTUD7A C15orf16 CEZANNE2 OTUD7	Homo sapiens (human)	1	1
P43304	Glycerol-3-phosphate dehydrogenase, mitochondrial	GPD2	Homo sapiens (human)	2	1	cancer central nervous system cancer citrullinemia communication disorder diabetes mellitus embryoma esophagus squamous cell carcinoma gliosarcoma high grade glioma insulinoma intellectual disability intrahepatic cholestasis language disorder learning disability mixed glioma motion sickness myopia osteoporosis reflex sympathetic dystrophy thyroid adenoma thyroid cancer thyroid gland carcinoma type 2 diabetes mellitus
P10827	Thyroid hormone receptor alpha	THRA EAR7 ERBA1 NR1A1 THRA1 THRA2	Homo sapiens (human)	0	1
Q5U5X0	Complex III assembly factor LYRM7	LYRM7 C5orf31 MZM1L	Homo sapiens (human)	0	1
Q01085	Nucleolysin TIAR	TIAL1	Homo sapiens (human)	2	1
Q13614	Myotubularin-related protein 2	MTMR2 KIAA1073	Homo sapiens (human)	0	1	Bell's palsy Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease agenesis of the corpus callosum with peripheral neuropathy agnosia axonal neuropathy cancer centronuclear myopathy X-linked centronuclear myopathy clubfoot congenital structural myopathy demyelinating polyneuropathy developmental coordination disorder facial nerve disease facial paralysis familial periodic paralysis glaucoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 motor peripheral neuropathy myopathy neurodegenerative disease neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease polyneuropathy scoliosis sensory peripheral neuropathy stomach cancer stomach carcinoma

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