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 **110851 - 110875** 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
Q8NHL6	Leukocyte immunoglobulin-like receptor subfamily B member 1	LILRB1 ILT2 LIR1 MIR7	Homo sapiens (human)	4	11
Q8NHM5	Lysine-specific demethylase 2B	KDM2B CXXC2 FBL10 FBXL10 JHDM1B NDY1 PCCX2	Homo sapiens (human)	1	2
Q8NHP1	Aflatoxin B1 aldehyde reductase member 4	AKR7L AFAR3 AKR7A4	Homo sapiens (human)	0	1
Q8NHP6	Motile sperm domain-containing protein 2	MOSPD2	Homo sapiens (human)	0	1
Q8NHP8	Putative phospholipase B-like 2	PLBD2	Homo sapiens (human)	11	22
Q8NHQ9	ATP-dependent RNA helicase DDX55	DDX55 KIAA1595	Homo sapiens (human)	1	1
Q8NHS3	Major facilitator superfamily domain-containing protein 8	MFSD8 CLN7	Homo sapiens (human)	3	1
Q8NHS4	Clathrin heavy chain linker domain-containing protein 1	CLHC1 C2orf63	Homo sapiens (human)	0	1
Q8NHU0	Cancer/testis antigen family 45 member A3	CT45A3 CT45-3 CT45-4 CT45A4	Homo sapiens (human)	1	0
Q8NHU2	Cilia- and flagella-associated protein 61	CFAP61 C20orf26	Homo sapiens (human)	2	1
Q8NHU6	Tudor domain-containing protein 7	TDRD7 PCTAIRE2BP	Homo sapiens (human)	2	1
Q8NHV1	GTPase IMAP family member 7	GIMAP7 IAN7	Homo sapiens (human)	1	2
Q8NHV4	Protein NEDD1	NEDD1	Homo sapiens (human)	5	2
Q8NHV5	Modulator of smoothened protein	MOSMO ATTHOG C16orf52	Homo sapiens (human)	1	0
Q8NHW3	Transcription factor MafA	MAFA	Homo sapiens (human)	0	1
Q8NHW5	Putative ribosomal protein uL10-like	RPLP0P6	Homo sapiens (human)	0	1
Q8NHX9	Two pore channel protein 2	TPCN2 TPC2	Homo sapiens (human)	2	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
Q8NHY2	E3 ubiquitin-protein ligase COP1	COP1 RFWD2 RNF200	Homo sapiens (human)	1	2
Q8NHY6	Zinc finger protein 28 homolog	ZFP28 KIAA1431	Homo sapiens (human)	0	1
Q8NI08	Nuclear receptor coactivator 7	NCOA7 ERAP140 ESNA1	Homo sapiens (human)	0	1
Q8NI15	Fibroblast growth factor receptor 3 (Fragment)	FGFR3	Homo sapiens (human)	2	0
Q8NI16	Fibroblast growth factor receptor 3 (Fragment)	FGFR3	Homo sapiens (human)	2	0
Q8NI17	Interleukin-31 receptor subunit alpha	IL31RA CRL3 GPL	Homo sapiens (human)	10	0
Q8NI22	Multiple coagulation factor deficiency protein 2	MCFD2 SDNSF	Homo sapiens (human)	4	3	arteriosclerotic cardiovascular disease atherosclerosis blood coagulation disease cancer congenital afibrinogenemia congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia coronary artery disease embryoma factor V deficiency factor VII deficiency factor VIII deficiency hematopoietic system disease nutmeg liver obsolete inherited blood coagulation disease seminoma testicular cancer testicular germ cell cancer testis seminoma transient cerebral ischemia vertebrobasilar insufficiency vitamin K deficiency bleeding

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