GlyCosmos Portal

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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 **125801 - 125825** 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
Q96RV3	Pecanex-like protein 1	PCNX1 KIAA0805 KIAA0995 PCNX PCNXL1	Homo sapiens (human)	20	3
Q92854	Semaphorin-4D	SEMA4D C9orf164 CD100 SEMAJ	Homo sapiens (human)	20	41
P10253	Lysosomal alpha-glucosidase	GAA	Homo sapiens (human)	20	85	Becker muscular dystrophy Clouston syndrome Duchenne muscular dystrophy Fabry disease Friedreich ataxia 1 Friedreich ataxia aortic aneurysm ataxia telangiectasia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cancer cardiomyopathy cerebellar ataxia cerebellar disease chylomicron retention disease cystinuria cytochrome-c oxidase deficiency disease diaphragm disease disease of metabolism distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial periodic paralysis galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease VI glycogen storage disease VII glycogen storage disease hypertrophic cardiomyopathy isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lipid storage disease lysosomal storage disease membranous glomerulonephritis mitochondrial metabolism disease mitochondrial myopathy muscular dystrophy myopathy neurodegenerative disease neuromuscular disease obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy patent foramen ovale peroxisome biogenesis disorder 7A primary immunodeficiency disease sensorineural hearing loss thyroid gland anaplastic carcinoma
P47035	Nucleolar protein NET1	NET1 CFI1 ESC5 SRM8	Saccharomyces cerevisiae S288C	20	1
Q6UN15	Pre-mRNA 3'-end-processing factor FIP1	FIP1L1 FIP1 RHE	Homo sapiens (human)	20	4
Q8WYP5	Protein ELYS	AHCTF1 ELYS TMBS62	Homo sapiens (human)	20	2
Q12427	Protein STB3	STB3	Saccharomyces cerevisiae S288C	20	1
Q8TER0	Sushi, nidogen and EGF-like domain-containing protein 1	SNED1	Homo sapiens (human)	20	5
Q96PV0	Ras/Rap GTPase-activating protein SynGAP	SYNGAP1 KIAA1938	Homo sapiens (human)	20	1
Q9WVT0	Adhesion G protein-coupled receptor F5	Adgrf5 Gpr116 Gprhep	Rattus norvegicus (Norway rat)	20	0
Q8CJ11	Adhesion G-protein coupled receptor G2	Adgrg2 Gpr64 Re6	Rattus norvegicus (Norway rat)	20	0
Q9SD62	Putative receptor-like protein kinase At3g47110	At3g47110	Arabidopsis thaliana (thale cress)	20	0
Q6ZRP7	Sulfhydryl oxidase 2	QSOX2 QSCN6L1 SOXN	Homo sapiens (human)	20	7
O08710	Thyroglobulin	Tg Tgn	Mus musculus (house mouse)	20	0
P58751	Reelin	Reln	Rattus norvegicus (Norway rat)	20	0
P53708	Integrin alpha-8	ITGA8	Homo sapiens (human)	20	11
C0LGQ5	LRR receptor-like serine/threonine-protein kinase GSO1	GSO1 SGN3	Arabidopsis thaliana (thale cress)	20	0
O36633	Major surface glycoprotein G	G	Human respiratory syncytial virus B1	20	0
Q04995	Envelope glycoprotein gp150	env	Feline immunodeficiency virus (strain UK8)	20	0
Q9MYL0	Leptin receptor	LEPR OBR	Macaca mulatta (Rhesus monkey)	20	0
P26006	Integrin alpha-3	ITGA3 MSK18	Homo sapiens (human)	20	95
Q868Z9	Papilin	Ppn	Drosophila melanogaster (fruit fly)	20	1
Q60841	Reelin	Reln Rl	Mus musculus (house mouse)	20	12
Q9Y6R7	IgGFc-binding protein	FCGBP	Homo sapiens (human)	20	47
Q6R5N8	Toll-like receptor 13	Tlr13	Mus musculus (house mouse)	20	0

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