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 **2576 - 2600** 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
P0CJ87	Double homeobox protein 4-like protein 4	DUX4L4	Homo sapiens (human)	1	1
O75339	Cartilage intermediate layer protein 1	CILP	Homo sapiens (human)	17	19
Q8NH42	Olfactory receptor 4K13	OR4K13	Homo sapiens (human)	1	0
P54296	Myomesin-2	MYOM2	Homo sapiens (human)	2	1
Q9Y6D5	Brefeldin A-inhibited guanine nucleotide-exchange protein 2	ARFGEF2 ARFGEP2 BIG2	Homo sapiens (human)	2	2
Q9ULD6	Protein inturned	INTU KIAA1284 PDZD6 PDZK6	Homo sapiens (human)	2	1
P02748	Complement component C9	C9	Homo sapiens (human)	10	55
Q9Y2I6	Ninein-like protein	NINL KIAA0980 NLP	Homo sapiens (human)	0	1
P04629	High affinity nerve growth factor receptor	NTRK1 MTC TRK TRKA	Homo sapiens (human)	13	1
E7ETJ6	Gamma-glutamyltransferase 1 (Fragment)	GGT1	Homo sapiens (human)	1	0
S5CJY0	MHC class I antigen (Fragment)	HLA-A	Homo sapiens (human)	1	0
A0A6G7S6G2	MHC class I protein	HLA-B	Homo sapiens (human)	1	0
D5FWB5	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9BXG8	Spermatogenic leucine zipper protein 1	SPZ1 TSP1	Homo sapiens (human)	0	1
O43175	D-3-phosphoglycerate dehydrogenase	PHGDH PGDH3	Homo sapiens (human)	5	1
Q96MH6	DGAT1/2-independent enzyme synthesizing storage lipids	TMEM68	Homo sapiens (human)	1	0
P48546	Gastric inhibitory polypeptide receptor	GIPR	Homo sapiens (human)	2	0
Q8NHP6	Motile sperm domain-containing protein 2	MOSPD2	Homo sapiens (human)	0	1
G1ENJ5	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9NZP5	Olfactory receptor 5AC2	OR5AC2	Homo sapiens (human)	1	0
A0A2I6Q792	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
Q96JC1	Vam6/Vps39-like protein	VPS39 KIAA0770 TLP VAM6	Homo sapiens (human)	1	1
P48729	Casein kinase I isoform alpha	CSNK1A1	Homo sapiens (human)	0	1
A0A3B1EVQ0	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
Q8NHY0	Beta-1,4 N-acetylgalactosaminyltransferase 2	B4GALNT2 GALGT2	Homo sapiens (human)	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

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