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 **7776 - 7800** 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
A0A427AAV7	Xyloglucan endotransglucosylase/hydrolase	B296_00013413	Ensete ventricosum	1	0
A0A426YWF8	Xyloglucan endotransglucosylase/hydrolase	B296_00014281	Ensete ventricosum	1	0
A0A426ZVH8	GH16 domain-containing protein	B296_00018353	Ensete ventricosum	1	0
A0A426ZQ91	Xyloglucan endotransglucosylase/hydrolase (Fragment)	B296_00038419	Ensete ventricosum	1	0
A0A426X2R1	Xyloglucan endotransglucosylase/hydrolase	B296_00052383	Ensete ventricosum	1	0
A0A426Y0H4	Xyloglucan endotransglucosylase/hydrolase (Fragment)	B296_00055249	Ensete ventricosum	1	0
P61769	Beta-2-microglobulin	B2M	Homo sapiens (human)	12	2
P01887	Beta-2-microglobulin	B2m	Mus musculus (house mouse)	0	1
W8AEU2	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	B3G2P	Ceratitis capitata (Mediterranean fruit fly)	1	0
V5H1C4	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase (Fragment)	B3G2P	Anoplophora glabripennis (Asian longhorned beetle)	1	0
W8BLI9	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	B3G2S	Ceratitis capitata (Mediterranean fruit fly)	1	0
A0A0S7IMB1	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	B3GA1	Poeciliopsis prolifica (blackstripe livebearer)	1	0
A0A0S7IRR7	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase (Fragment)	B3GA1	Poeciliopsis prolifica (blackstripe livebearer)	1	0
A0A0S7IPP7	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase (Fragment)	B3GA1	Poeciliopsis prolifica (blackstripe livebearer)	1	0
A0A0S7IB68	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase (Fragment)	B3GA3	Poeciliopsis prolifica (blackstripe livebearer)	1	0
U6CR01	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	B3GA3	Neogale vison (American mink)	1	0
Q864U6	UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 1	B3GALNT1 B3GALT3	Sus scrofa (pig)	5	0
O75752	UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 1	B3GALNT1 B3GALT3	Homo sapiens (human)	9	1	brain cancer cancer lung cancer lung non-small cell carcinoma pancreatic ductal adenocarcinoma
Q5RAL7	UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 1	B3GALNT1 B3GALT3	Pongo abelii (Sumatran orangutan)	5	0
R4X5Z4	Hexosyltransferase	B3GALNT1	Homo sapiens (human)	1	0
A0A494C0Y5	Hexosyltransferase (Fragment)	B3GALNT1	Homo sapiens (human)	1	0
Q49AT3	Hexosyltransferase	B3GALNT1	Homo sapiens (human)	1	0
Q8NCR0	UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 2	B3GALNT2	Homo sapiens (human)	2	0	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia 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 bilateral optic nerve hypoplasia blindness breast cancer breast carcinoma cancer cataract cerebral degeneration choreatic disease coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A11 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism depressive disorder developmental coordination disorder distal myopathy dysthymic disorder dystonia embryoma epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis focal epilepsy fundus dystrophy glaucoma hepatocellular carcinoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lissencephaly liver cancer major depressive disorder mechanical strabismus melancholic depression meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia neurotic disorder 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 infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy partial motor epilepsy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder stereotypic movement disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type syndromic X-linked intellectual disability type 10 visual epilepsy
Q9Y5Z6	Beta-1,3-galactosyltransferase 1	B3GALT1	Homo sapiens (human)	2	0	Peters plus syndrome adenocarcinoma adenoma cribriform carcinoma granular cell carcinoma tubular adenocarcinoma
Q7JK25	Beta-1,3-galactosyltransferase 1	B3GALT1	Pan paniscus (pygmy chimpanzee)	2	0

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