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 **676 - 700** 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
Q40235	Receptor-like protein Cf-9	CF-9	Solanum pimpinellifolium	21	0
P18490	Protein pecanex	pcx	Drosophila melanogaster (fruit fly)	21	0
A5DZQ4	Maintenance of telomere capping protein 6	MTC6	Lodderomyces elongisporus NRRL YB-4239	21	0
C0LGJ1	Probable LRR receptor-like serine/threonine-protein kinase At1g74360	At1g74360	Arabidopsis thaliana (thale cress)	21	0
A2A654	Bromodomain PHD finger transcription factor	Bptf	Mus musculus (house mouse)	21	5
P15999	ATP synthase subunit alpha, mitochondrial	Atp5f1a Atp5a1	Rattus norvegicus (Norway rat)	21	1
O95817	BAG family molecular chaperone regulator 3	BAG3 BIS	Homo sapiens (human)	21	2
Q02505	Mucin-3A	MUC3A MUC3	Homo sapiens (human)	21	1
Q9UHD9	Ubiquilin-2	UBQLN2 N4BP4 PLIC2	Homo sapiens (human)	21	3
Q9EPN1	Neurobeachin	Nbea Lyst2	Mus musculus (house mouse)	21	6
O94907	Dickkopf-related protein 1	DKK1	Homo sapiens (human)	21	1
Q76M96	Coiled-coil domain-containing protein 80	CCDC80 DRO1 URB	Homo sapiens (human)	21	7
Q8AV57	Protein sidekick-2	SDK2	Gallus gallus (chicken)	21	0
Q5XNR9	Leukemia inhibitory factor receptor	LIFR	Canis lupus familiaris (dog)	20	0
Q12265	Ribose-phosphate pyrophosphokinase 5	PRS5 PRPS5	Saccharomyces cerevisiae S288C	20	1
P39113	Regulatory protein CAT8	CAT8 MSP8	Saccharomyces cerevisiae S288C	20	1
Q14515	SPARC-like protein 1	SPARCL1	Homo sapiens (human)	20	19
Q9C637	Receptor-like protein 6	RLP6	Arabidopsis thaliana (thale cress)	20	0
E1C8P7	Cell adhesion molecule DSCAML1	DSCAML1	Gallus gallus (chicken)	20	0
P52583	Vascular endothelial growth factor receptor 2	KDR EK1 FLK-1	Coturnix japonica (Japanese quail)	20	0
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

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