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 **15151 - 15175** 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
A0A7I2V3X6	Angiotensin-converting enzyme	ACE2	Homo sapiens (human)	4	0
Q8L7W8	Alpha-L-fucosidase 2	FUC95A AXY8	Arabidopsis thaliana (thale cress)	4	0
P31042	T-cell-specific surface glycoprotein CD28	Cd28	Rattus norvegicus (Norway rat)	4	0
B8A4W9	Lysyl oxidase homolog 3B	loxl3b	Danio rerio (zebrafish)	4	0
Q91WJ2	Solute carrier family 22 (organic cation transporter), member 26	Slc22a26 BC014805	Mus musculus (house mouse)	4	0
A5A6P2	Acid ceramidase	ASAH1	Pan troglodytes (chimpanzee)	4	0
Q5DRD8	Protocadherin beta-11	PCDHB11	Pan troglodytes (chimpanzee)	4	0
Q22396	Zinc metalloproteinase nas-20	nas-20	Caenorhabditis elegans	4	0
O75311	Glycine receptor subunit alpha-3	GLRA3	Homo sapiens (human)	4	1
Q8JIY1	Disintegrin and metalloproteinase domain-containing protein 10	adam10 kuz	Xenopus laevis (African clawed frog)	4	0
A7Y2W8	Sodium- and chloride-dependent glycine transporter 1	slc6a9 glyt1	Xenopus laevis (African clawed frog)	4	0
Q09500	Cystinosin homolog	ctns-1	Caenorhabditis elegans	4	0
A0A7K6A403	Angiotensin-converting enzyme (Fragment)	Ace	Onychorhynchus coronatus	4	0
Q3L245	Pyranose dehydrogenase 1	pdh1	Leucoagaricus meleagris	4	0
P86044	Anoctamin-9	Ano9 Tmem16j	Mus musculus (house mouse)	4	0
P68327	Envelope glycoprotein D	gD GP17/18	Equine herpesvirus type 1 (strain Kentucky D)	4	0
A0A1E1FFN4	FAD-binding monooxygenase prhK	prhK	Penicillium brasilianum	4	0
Q91WV4	Parathyroid hormone/parathyroid hormone-related peptide receptor	Pth1r	Mus musculus (house mouse)	4	0
Q810C0	SLIT and NTRK-like protein 2	Slitrk2	Mus musculus (house mouse)	4	3
B2RWT9	Plexin B1	Plxnb1	Mus musculus (house mouse)	4	0
Q6NT32	Carboxylesterase 5A	CES5A CES7	Homo sapiens (human)	4	0
A0A140T8T2	Slit guidance ligand 2	Slit2	Mus musculus (house mouse)	4	0
Q9UN74	Protocadherin alpha-4	PCDHA4	Homo sapiens (human)	4	0
Q15075	Early endosome antigen 1	EEA1 ZFYVE2	Homo sapiens (human)	4	2
Q9Y2B1	Ribitol-5-phosphate xylosyltransferase 1	RXYLT1 TMEM5	Homo sapiens (human)	4	2	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Turner syndrome Walker-Warburg syndrome 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 cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A10 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma gonadal dysgenesis hydranencephaly hydrocephalus intellectual disability learning disability limb-girdle muscular dystrophy lissencephaly microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy 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 septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy

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