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 **16101 - 16125** 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
Q07E16	Cystic fibrosis transmembrane conductance regulator	CFTR ABCC7	Mustela putorius furo (domestic ferret)	2	0
P34158	Cystic fibrosis transmembrane conductance regulator	Cftr Abcc7	Rattus norvegicus (Norway rat)	2	0
Q00555	Cystic fibrosis transmembrane conductance regulator	CFTR ABCC7	Ovis aries (sheep)	2	0
Q07DZ6	Cystic fibrosis transmembrane conductance regulator	CFTR ABCC7	Ornithorhynchus anatinus (platypus)	3	0
Q2QL83	Cystic fibrosis transmembrane conductance regulator	CFTR ABCC7	Microcebus murinus (gray mouse lemur)	2	0
Q5U820	Cystic fibrosis transmembrane conductance regulator	CFTR ABCC7	Canis lupus familiaris (dog)	3	0
P17261	Cystine transporter	ERS1	Saccharomyces cerevisiae S288C	1	0
Q5RAG7	Cystine/glutamate transporter	SLC7A11	Pongo abelii (Sumatran orangutan)	1	0
Q9UPY5	Cystine/glutamate transporter	SLC7A11	Homo sapiens (human)	2	1
Q3TC99	Cystinosin	Ctns	Mus musculus (house mouse)	4	0
Q542U5	Cystinosin	Ctns	Mus musculus (house mouse)	4	0
A7MB63	Cystinosin	CTNS	Bos taurus (cattle)	5	0
P57757	Cystinosin	Ctns	Mus musculus (house mouse)	6	1
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
P57758	Cystinosin homolog	At5g40670	Arabidopsis thaliana (thale cress)	2	0
Q09500	Cystinosin homolog	ctns-1	Caenorhabditis elegans	4	0
A8WN56	Cystinosin homolog	ctns-1	Caenorhabditis briggsae	4	0
Q9VCR7	Cystinosin homolog	CG17119	Drosophila melanogaster (fruit fly)	2	1
P32320	Cytidine deaminase	CDA CDD	Homo sapiens (human)	0	1
V4YI37	Cytochrome C family oxidase subunit III subfamily protein (Fragment)	TGVEG_442760	Toxoplasma gondii VEG	0	1
Q3LFU0	Cytochrome P450 1A1	CYP1A1	Balaenoptera acutorostrata (minke whale)	1	0
P56591	Cytochrome P450 1A1	CYP1A1	Ovis aries (sheep)	1	0
P56590	Cytochrome P450 1A1	CYP1A1	Canis lupus familiaris (dog)	1	0
Q5KQT7	Cytochrome P450 1A1	CYP1A1	Felis catus (domestic cat)	1	0
Q6GUR1	Cytochrome P450 1A1	CYP1A1	Macaca mulatta (Rhesus monkey)	1	0

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