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 **123776 - 123800** 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
A0A8T3E2L0	P2X purinoceptor	AGOR_G00021070	Albula goreensis	1	0
A0A8T3EBJ8	Peptidyl-glycine alpha-amidating monooxygenase	AGOR_G00013330	Albula goreensis	1	0
Q9H9G7	Protein argonaute-3	AGO3 EIF2C3	Homo sapiens (human)	2	1
Q9UKV8	Protein argonaute-2	AGO2 EIF2C2	Homo sapiens (human)	1	2
Q9UL18	Protein argonaute-1	AGO1 EIF2C1	Homo sapiens (human)	1	2
Q6ZNB7	Alkylglycerol monooxygenase	AGMO TMEM195	Homo sapiens (human)	1	1
A0A6G0SYB1	Potassium channel subfamily K member 1	AGLY_015942	Aphis glycines (soybean aphid)	1	0
A0A6G0T1G3	Angiotensin-converting enzyme	AGLY_015381	Aphis glycines (soybean aphid)	1	0
A0A6G0T7K2	Noggin	AGLY_013420	Aphis glycines (soybean aphid)	1	0
A0A6G0TBY5	EF-hand domain-containing protein	AGLY_011837	Aphis glycines (soybean aphid)	1	0
A0A6G0TMS3	Protein adenylyltransferase Fic	AGLY_007703	Aphis glycines (soybean aphid)	1	0
A0A6G0TZW6	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	AGLY_003512	Aphis glycines (soybean aphid)	1	0
A0A6G0U737	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	AGLY_000132	Aphis glycines (soybean aphid)	1	0
Q750Z6	Vacuolar membrane protease	AGL209W	Eremothecium gossypii ATCC 10895	4	0
Q38836	Agamous-like MADS-box protein AGL11	AGL11 STK	Arabidopsis thaliana (thale cress)	0	1
P35573	Glycogen debranching enzyme	AGL GDE	Homo sapiens (human)	2	1	Duchenne muscular dystrophy Laron syndrome achondroplasia acute promyelocytic leukemia atrichia with papular lesions 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 bladder carcinoma cancer cardiomyopathy colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital muscular dystrophy cystinuria disease of metabolism distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hyperlipidemia familial partial lipodystrophy familial periodic paralysis galactosemia giardiasis glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatitis C hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels kidney failure large intestine cancer limb-girdle muscular dystrophy lipoatrophic diabetes mellitus lipodystrophy liver cirrhosis lung cancer lung non-small cell carcinoma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy nodular nonsuppurative panniculitis 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 panniculitis primary immunodeficiency disease rippling muscle disease 2 uremia urinary bladder cancer
Q86SA8	Androgenic gland hormone	AGH	Porcellio dilatatus	1	0
Q8I7X1	Androgenic gland hormone	AGH	Porcellio scaber	1	0
O95081	Arf-GAP domain and FG repeat-containing protein 2	AGFG2 HRBL RABR	Homo sapiens (human)	14	2
Q2TA45	Arf-GAP domain and FG repeat-containing protein 1	AGFG1 HRB RIP	Bos taurus (cattle)	1	0
P52594	Arf-GAP domain and FG repeat-containing protein 1	AGFG1 HRB RAB RIP	Homo sapiens (human)	40	3
A0A9N9CWJ1	6172_t:CDS:1	AGERDE_LOCUS9938	Ambispora gerdemannii	2	0
A0A9N9ASN1	12922_t:CDS:1	AGERDE_LOCUS6147	Ambispora gerdemannii	1	0
A0A9N8Z141	4454_t:CDS:1	AGERDE_LOCUS2151	Ambispora gerdemannii	1	0
Q28173	Advanced glycosylation end product-specific receptor	AGER RAGE	Bos taurus (cattle)	2	0

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