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 **201 - 225** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
P43652	Afamin	AFM ALB2 ALBA	Homo sapiens (human)	6	67
P05546	Heparin cofactor 2	SERPIND1 HCF2	Homo sapiens (human)	14	66
Q99571	P2X purinoceptor 4	P2RX4	Homo sapiens (human)	7	66
P02710	Acetylcholine receptor subunit alpha	CHRNA1	Tetronarce californica (Pacific electric ray)	1	66
P16422	Epithelial cell adhesion molecule	EPCAM GA733-2 M1S2 M4S1 MIC18 TACSTD1 TROP1	Homo sapiens (human)	6	66
P50895	Basal cell adhesion molecule	BCAM LU MSK19	Homo sapiens (human)	7	66
P14625	Endoplasmin	HSP90B1 GRP94 HSPC4 TRA1	Homo sapiens (human)	15	66
O75503	Bis(monoacylglycero)phosphate synthase CLN5	CLN5 BMPS	Homo sapiens (human)	8	66	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 Lafora disease MERRF syndrome Pick's disease Reye syndrome Unverricht-Lundborg syndrome agnosia blepharospasm blindness brain disease cerebellar ataxia cerebellar disease cerebral degeneration early myoclonic encephalopathy epilepsy eye disease focal hand dystonia intellectual disability learning disability neurodegenerative disease 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 retinal degeneration visual epilepsy
P04216	Thy-1 membrane glycoprotein	THY1	Homo sapiens (human)	4	66
O60637	Tetraspanin-3	TSPAN3 TM4SF8	Homo sapiens (human)	7	65
O00592	Podocalyxin	PODXL PCLP PCLP1	Homo sapiens (human)	72	65
P00747	Plasminogen	PLG	Homo sapiens (human)	17	65
Q02487	Desmocollin-2	DSC2 CDHF2 DSC3	Homo sapiens (human)	6	65
P20701	Integrin alpha-L	ITGAL CD11A	Homo sapiens (human)	12	64
P17948	Vascular endothelial growth factor receptor 1	FLT1 FLT FRT VEGFR1	Homo sapiens (human)	13	64
Q16563	Synaptophysin-like protein 1	SYPL1 SYPL	Homo sapiens (human)	5	64
P26201	Platelet glycoprotein 4	CD36 PAS4	Bos taurus (cattle)	8	64
Q9UGT4	Sushi domain-containing protein 2	SUSD2	Homo sapiens (human)	7	64
P43251	Biotinidase	BTD	Homo sapiens (human)	6	63
P34810	Macrosialin	CD68	Homo sapiens (human)	13	63
P35613	Basigin	BSG	Homo sapiens (human)	12	63
P20774	Mimecan	OGN OIF SLRR3A	Homo sapiens (human)	4	63
Q62005	Zona pellucida sperm-binding protein 1	Zp1	Mus musculus (house mouse)	6	63
O00754	Lysosomal alpha-mannosidase	MAN2B1 LAMAN MANB	Homo sapiens (human)	14	63	IgA glomerulonephritis Klippel-Feil syndrome age related macular degeneration alpha-mannosidosis aspartylglucosaminuria cerebral degeneration congenital nystagmus degeneration of macula and posterior pole dissociated nystagmus fucosidosis gingival hypertrophy gingival overgrowth glycogen storage disease II hypertrichosis inguinal hernia intellectual disability learning disability lingual-facial-buccal dyskinesia lysosomal storage disease macular degeneration methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency movement disease mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis pathologic nystagmus retinal degeneration sensorineural hearing loss spondylolisthesis spontaneous ocular nystagmus
P19823	Inter-alpha-trypsin inhibitor heavy chain H2	ITIH2 IGHEP2	Homo sapiens (human)	17	62

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