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 **113551 - 113575** 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
O70583	E3 ubiquitin-protein ligase Midline-1	Mid1 Fxy Trim18	Mus musculus (house mouse)	0	1
F6QPR1	Prohibitin (Fragment)	Phb2	Mus musculus (house mouse)	0	1
Q9VXY2	MAP kinase-activating death domain protein	Rab3-GEF	Drosophila melanogaster (fruit fly)	0	1
P52298	Nuclear cap-binding protein subunit 2	NCBP2 CBP20	Homo sapiens (human)	0	1
Q8VE10	N-alpha-acetyltransferase 40	Naa40 Nat11 Patt1	Mus musculus (house mouse)	0	1
Q9NQ29	Putative RNA-binding protein Luc7-like 1	LUC7L LUC7L1	Homo sapiens (human)	0	1
P11714	Cytochrome P450 2D9	Cyp2d9 Cyp2d-9	Mus musculus (house mouse)	0	1
Q9R061	Cytosolic Fe-S cluster assembly factor NUBP2	Nubp2	Mus musculus (house mouse)	0	1
O88456	Calpain small subunit 1	Capns1 Capn4	Mus musculus (house mouse)	0	1
Q96HS1	Serine/threonine-protein phosphatase PGAM5, mitochondrial	PGAM5	Homo sapiens (human)	0	1
Q8N5F7	NF-kappa-B-activating protein	NKAP	Homo sapiens (human)	1	1
Q9NX61	Transmembrane protein 161A	TMEM161A	Homo sapiens (human)	2	1
Q13630	GDP-L-fucose synthase	GFUS SDR4E1 TSTA3	Homo sapiens (human)	0	1
Q9SW80	BEL1-like homeodomain protein 2	BLH2 SAW1	Arabidopsis thaliana (thale cress)	0	1
P57776	Elongation factor 1-delta	Eef1d	Mus musculus (house mouse)	0	1
Q9FIA3	Gb\|AAF16663.1	At5g55040	Arabidopsis thaliana (thale cress)	0	1
O43747	AP-1 complex subunit gamma-1	AP1G1 ADTG CLAPG1	Homo sapiens (human)	0	1
Q4DXX9	ABC transporter, putative	Tc00.1047053510431.150	Trypanosoma cruzi strain CL Brener	0	1
Q6PEY2	Tubulin alpha-3E chain	TUBA3E	Homo sapiens (human)	0	1
Q99666	RANBP2-like and GRIP domain-containing protein 5/6	RGPD5 RGPD6 RANBP2L1 RANBP2L2 RGP5 RGP6 RGP7 RGPD7	Homo sapiens (human)	2	1
Q6P4T2	U5 small nuclear ribonucleoprotein 200 kDa helicase	Snrnp200 Kiaa0788	Mus musculus (house mouse)	1	1
Q4DMX9	3-hydroxyisobutyryl-CoA hydrolase	Tc00.1047053511529.160	Trypanosoma cruzi strain CL Brener	0	1
P11217	Glycogen phosphorylase, muscle form	PYGM	Homo sapiens (human)	0	1	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Peutz-Jeghers syndrome X-linked myopathy with excessive autophagy 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 bacterial sepsis breast cancer breast carcinoma cancer carcinoma cholestasis coronary artery disease cystinuria disease of metabolism distal myopathy facioscapulohumeral muscular dystrophy familial adenomatous polyposis familial periodic paralysis galactosemia gastrinoma glucosephosphate dehydrogenase deficiency 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 V glycogen storage disease VI glycogen storage disease VII glycogen storage disease gout head and neck squamous cell carcinoma insulinoma invasive lobular carcinoma islet cell tumor isolated elevated serum creatine phosphokinase levels kidney failure limb-girdle muscular dystrophy lipoma melanoma multiple endocrine neoplasia type 1 multiple symmetric lipomatosis muscular dystrophy myoglobinuria myopathy 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 pleomorphic lipoma pre-eclampsia pseudosarcomatous fibromatosis sarcomatoid carcinoma skin melanoma vitelliform macular dystrophy von Hippel-Lindau disease
Q02094	Ammonium transporter Rh type A	RHAG RH50	Homo sapiens (human)	3	1
O35826	Bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase	Gne Glcne	Rattus norvegicus (Norway rat)	0	1

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