GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q9UBT3	Dickkopf-related protein 4	DKK4	0	1
Q6W2J9	BCL-6 corepressor	BCOR KIAA1575	12	1
P63010	AP-2 complex subunit beta	AP2B1 ADTB2 CLAPB1	2	1
P0CJ87	Double homeobox protein 4-like protein 4	DUX4L4	1	1
P54296	Myomesin-2	MYOM2	2	1
Q9ULD6	Protein inturned	INTU KIAA1284 PDZD6 PDZK6	2	1
Q9Y2I6	Ninein-like protein	NINL KIAA0980 NLP	0	1
P04629	High affinity nerve growth factor receptor	NTRK1 MTC TRK TRKA	13	1
Q9BXG8	Spermatogenic leucine zipper protein 1	SPZ1 TSP1	0	1
O43175	D-3-phosphoglycerate dehydrogenase	PHGDH PGDH3	5	1
Q8NHP6	Motile sperm domain-containing protein 2	MOSPD2	0	1
Q96JC1	Vam6/Vps39-like protein	VPS39 KIAA0770 TLP VAM6	1	1
P48729	Casein kinase I isoform alpha	CSNK1A1	0	1
Q8NHY0	Beta-1,4 N-acetylgalactosaminyltransferase 2	B4GALNT2 GALGT2	0	1	Duchenne muscular dystrophy autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 campomelic dysplasia cancer carcinoma cerebrotendinous xanthomatosis congenital muscular dystrophy coronary artery disease distal myopathy embryoma facioscapulohumeral muscular dystrophy limb-girdle muscular dystrophy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 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 rippling muscle disease 2 sarcomatoid carcinoma
P0C7P4	Putative cytochrome b-c1 complex subunit Rieske-like protein 1	UQCRFS1P1 UQCRFSL1	2	1
Q99541	Perilipin-2	PLIN2 ADFP	1	1
Q9P219	Protein Daple	CCDC88C DAPLE KIAA1509	7	1
Q13516	Oligodendrocyte transcription factor 2	OLIG2 BHLHB1 BHLHE19 PRKCBP2 RACK17	1	1
Q5T6J7	Probable gluconokinase	IDNK C9orf103	1	1
Q03252	Lamin-B2	LMNB2 LMN2	5	1
P53611	Geranylgeranyl transferase type-2 subunit beta	RABGGTB GGTB	0	1
Q5T442	Gap junction gamma-2 protein	GJC2 GJA12	1	1
Q86VR7	V-set and immunoglobulin domain-containing protein 10-like	VSIG10L	10	1
Q16891	MICOS complex subunit MIC60	IMMT HMP MIC60 MINOS2	0	1
Q9NVK5	FGFR1 oncogene partner 2	FGFR1OP2	0	1

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