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 **126126 - 126150** 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
O15118	NPC intracellular cholesterol transporter 1	NPC1	Homo sapiens (human)	26	32	Niemann-Pick disease type C1
Q03164	Histone-lysine N-methyltransferase 2A	KMT2A ALL1 CXXC7 HRX HTRX MLL MLL1 TRX1	Homo sapiens (human)	26	6
P00451	Coagulation factor VIII	F8 F8C	Homo sapiens (human)	26	61
N1P212	Periplasmic acid trehalase ATC1	CENPK1137D_1727	Saccharomyces cerevisiae CEN.PK113-7D	26	0
Q80T79	CUB and sushi domain-containing protein 3	Csmd3 Kiaa1894	Mus musculus (house mouse)	26	14
Q8BNA6	Protocadherin Fat 3	Fat3 Gm1132 Gm510	Mus musculus (house mouse)	26	9
P12111	Collagen alpha-3(VI) chain	COL6A3	Homo sapiens (human)	26	97
Q9ERB4	Versican core protein (Fragments)	Vcan Cspg2	Rattus norvegicus (Norway rat)	26	0
Q6UXD5	Seizure 6-like protein 2	SEZ6L2 PSK	Homo sapiens (human)	26	22
P20888	Envelope glycoprotein gp160	env	Human immunodeficiency virus type 1 (OYI ISOLATE)	26	0
Q9ZUK3	Receptor-like protein 19	RLP19	Arabidopsis thaliana (thale cress)	26	0
Q05707	Collagen alpha-1(XIV) chain	COL14A1 UND	Homo sapiens (human)	26	108
Q9ULT8	E3 ubiquitin-protein ligase HECTD1	HECTD1 KIAA1131	Homo sapiens (human)	26	6
O43451	Maltase-glucoamylase	MGAM MGA MGAML	Homo sapiens (human)	26	110	Duchenne muscular dystrophy Fabry disease Gaucher's disease Gerstmann-Straussler-Scheinker syndrome Gorham's disease Japanese encephalitis adenocarcinoma adenoma amyotrophic lateral sclerosis arteriosclerotic cardiovascular disease atherosclerosis 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 brachydactyly type C brachydactyly breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease chylomicron retention disease congenital disorder of glycosylation congenital muscular dystrophy coronary artery disease cribriform carcinoma cystic fibrosis cystinuria dengue disease depressive disorder diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy distal myopathy embryoma endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial periodic paralysis galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease granular cell carcinoma heart disease hyperglycemia hypertrophic cardiomyopathy hypoglycemia limb-girdle muscular dystrophy lipid storage disease lysosomal storage disease major depressive disorder melancholic depression muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myotonic dystrophy type 1 myotonic dystrophy type 2 neuromuscular disease nutmeg liver obesity 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 obsolete constipation obsolete melancholia oculopharyngeal muscular dystrophy progressive muscular atrophy prolactinoma punctate palmoplantar keratoderma type III rippling muscle disease 2 squamous cell carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus viral infectious disease yellow fever
G5ECE3	Laminin subunit alpha lam-3	lam-3 lama1/2	Caenorhabditis elegans	27	0
O00461	Golgi integral membrane protein 4	GOLIM4 GIMPC GOLPH4 GPP130	Homo sapiens (human)	27	8
Q76LX8	A disintegrin and metalloproteinase with thrombospondin motifs 13	ADAMTS13 C9orf8	Homo sapiens (human)	27	15
P82279	Protein crumbs homolog 1	CRB1	Homo sapiens (human)	27	1
P23423	Envelope glycoprotein gp160	env	Visna lentivirus (strain 1514 / clone LV1-1KS2)	27	0
Q8IZP9	Adhesion G-protein coupled receptor G2	ADGRG2 GPR64 HE6 TM7LN2	Homo sapiens (human)	27	6
O96175	Male gametocyte surface protein P230p	PFS230P PF230P PfsMR5 S230P	Plasmodium falciparum 3D7	27	0
Q9BZC7	ATP-binding cassette sub-family A member 2	ABCA2 ABC2 KIAA1062	Homo sapiens (human)	27	14
P54727	UV excision repair protein RAD23 homolog B	RAD23B	Homo sapiens (human)	27	2
P18040	Envelope glycoprotein gp160	env	Human immunodeficiency virus type 2 (ISOLATE GHANA-1)	27	0
P35961	Envelope glycoprotein gp160	env	Human immunodeficiency virus type 1 (isolate YU2)	27	0

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