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 **123826 - 123850** 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
A0A9C6X2Z6	Voltage-dependent calcium channel type A subunit alpha-1 isoform X1	LOC113211476	Frankliniella occidentalis (western flower thrips)	1	0
V9SRH7	Matrix protein 2	M2 M	Influenza A virus (A/Peru/PER109/2010(H3N2))	1	0
L8AVA0	Non-structural glycoprotein 4	NSP4	Bovine rotavirus G6	2	0
Q06BI4	Xyloglucan endotransglucosylase/hydrolase	XTH3	Cucumis melo (muskmelon)	1	0
A0A2H4RN86	Matrix protein 2	M2 M	Influenza A virus (A/Nicaragua/9156_03/2016(H3N2))	1	0
C8CRV2	Matrix protein 2	M2 M	Influenza A virus (A/Wisconsin/13/2009(H1N1))	1	0
A0A8B7QB28	Voltage-dependent L-type calcium channel subunit alpha-1F isoform X6	CACNA1F	Hipposideros armiger (great roundleaf bat)	1	0
P13533	Myosin-6	MYH6 MYHCA	Homo sapiens (human)	0	1
V4MFY9	Xyloglucan endotransglucosylase/hydrolase	EUTSA_v10025803mg	Eutrema salsugineum	1	0
A0A6I9QLI2	Xyloglucan endotransglucosylase/hydrolase	LOC105037481	Elaeis guineensis (African oil palm)	1	0
A0A852DX75	Rhodopsin (Fragment)	Rho	Vidua macroura (Pin-tailed whydah)	2	0
D3YZU1	SH3 and multiple ankyrin repeat domains protein 1	Shank1	Mus musculus (house mouse)	13	1
A0A1I9TKU1	Matrix protein 2	M2 M	Influenza A virus (A/Hawaii/67/2016(H3N2))	1	0
A0A0X8EIU7	Matrix protein 2	M2 M	Influenza A virus (A/Florida/87/2015(H3N2))	1	0
Q9D8S4	Oligoribonuclease, mitochondrial	Rexo2 Smfn	Mus musculus (house mouse)	0	1
A0A6P8HZF2	Tartrate-resistant acid phosphatase type 5	LOC116294565	Actinia tenebrosa (Australian red waratah sea anemone)	1	0
A0A1U8NZJ4	UDP-arabinopyranose mutase	LOC107953490	Gossypium hirsutum (cotton)	1	0
Q95227	Kappa-casein (Fragment)	CSN3 CSN10 CSNK	Ovibos moschatus (muskox)	8	0
O60931	Cystinosin	CTNS	Homo sapiens (human)	7	0	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Fanconi anemia Fanconi syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome achondroplasia androgen insensitivity syndrome anhidrosis 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 vaginosis bone disease cartilage disease cerebral degeneration cone-rod dystrophy connective tissue disease cystinosis diabetes mellitus diabetic ketoacidosis disease of metabolism distal myopathy eunuchism exocrine pancreatic insufficiency facioscapulohumeral muscular dystrophy fundus albipunctatus glomerulonephritis hypogonadism hypohidrosis hypokalemia hypophosphatemia kidney disease kidney failure limb-girdle muscular dystrophy lysosomal storage disease male infertility muscular dystrophy nephritis nephrolithiasis nephrosis obsolete asthenopia 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 oculopharyngeal muscular dystrophy osteomalacia premature menopause proteinuria pyoureter recurrent corneal erosion retinal disease retinitis pigmentosa retinitis rickets spondyloepimetaphyseal dysplasia, Sponastrime type uric acid nephrolithiasis vaginitis vulvitis vulvovaginitis
A0A851N9R3	Hyaluronidase (Fragment)	Hyal1	Campylorhamphus procurvoides	1	0
Q7SYC9	Choline transporter-like protein 2	slc44a2 ctl2	Danio rerio (zebrafish)	5	0
A0A8L2QGY3	P2X purinoceptor	P2rx3	Rattus norvegicus (Norway rat)	1	0
Q9NSP4	Centromere protein M	CENPM C22orf18 ICEN39 PANE1	Homo sapiens (human)	2	1
A0A671P3W9	Cathepsin D-like	LOC107695135	Sinocyclocheilus anshuiensis	2	0
B3LP27	Topoisomerase I damage affected protein 7	TDA7	Saccharomyces cerevisiae RM11-1a	6	0

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