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 **2876 - 2900** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▲	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q96RT6	cTAGE family member 2	CTAGE1 CTAGE2	Homo sapiens (human)	0	1
Q13363	C-terminal-binding protein 1	CTBP1 CTBP	Homo sapiens (human)	0	1
P56545	C-terminal-binding protein 2	CTBP2	Homo sapiens (human)	0	1
Q01459	Di-N-acetylchitobiase	CTBS CTB	Homo sapiens (human)	4	20	Clouston syndrome allergic rhinitis amyotrophic lateral sclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer cholera colon cancer colon carcinoma colonic benign neoplasm colorectal cancer hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease large intestine cancer liver cancer progressive muscular atrophy prostate cancer prostate carcinoma ulcerative colitis vasomotor rhinitis
P49711	Transcriptional repressor CTCF	CTCF	Homo sapiens (human)	0	1
Q9Y5B0	RNA polymerase II subunit A C-terminal domain phosphatase	CTDP1 FCP1	Homo sapiens (human)	4	2
Q9GZU7	Carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1	CTDSP1 NIF3 NLIIF SCP1	Homo sapiens (human)	1	1
Q6FHL8	CCN family member 2	CTGF	Homo sapiens (human)	1	0
Q5M8T4	CCN family member 2	CTGF	Homo sapiens (human)	1	0
P32929	Cystathionine gamma-lyase	CTH	Homo sapiens (human)	1	1
Q96CG8	Collagen triple helix repeat-containing protein 1	CTHRC1	Homo sapiens (human)	1	0
P16410	Cytotoxic T-lymphocyte protein 4	CTLA4 CD152	Homo sapiens (human)	2	0
P35221	Catenin alpha-1	CTNNA1	Homo sapiens (human)	2	2
P26232	Catenin alpha-2	CTNNA2 CAPR	Homo sapiens (human)	0	1
Q9UI47	Catenin alpha-3	CTNNA3	Homo sapiens (human)	1	1
Q9UBT7	Alpha-catulin	CTNNAL1	Homo sapiens (human)	1	1
P35222	Catenin beta-1	CTNNB1 CTNNB	Homo sapiens (human)	5	2
Q8WYA6	Beta-catenin-like protein 1	CTNNBL1 C20orf33	Homo sapiens (human)	2	1
O60716	Catenin delta-1	CTNND1 KIAA0384	Homo sapiens (human)	2	5
Q9UQB3	Catenin delta-2	CTNND2 NPRAP	Homo sapiens (human)	13	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
P17812	CTP synthase 1	CTPS1 CTPS	Homo sapiens (human)	1	3
Q9NRF8	CTP synthase 2	CTPS2	Homo sapiens (human)	0	1
Q6PD62	RNA polymerase-associated protein CTR9 homolog	CTR9 KIAA0155 SH2BP1	Homo sapiens (human)	0	1
Q99895	Chymotrypsin-C	CTRC CLCR	Homo sapiens (human)	4	0

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