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 **110876 - 110900** 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
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
Q5DRE6	Protocadherin alpha-6	PCDHA6	Pan troglodytes (chimpanzee)	4	0
D4D4Z2	Probable extracellular metalloproteinase 1	MEP1	Trichophyton verrucosum HKI 0517	4	0
P48022	3-hydroxy-3-methylglutaryl-coenzyme A reductase 2	HMG2	Solanum lycopersicum (tomato)	4	0
F4KG58	Exocyst complex component EXO70A3	EXO70A3	Arabidopsis thaliana (thale cress)	4	0
Q8AWC7	Alpha-(1,3)-fucosyltransferase 11	FUT11	Gallus gallus (chicken)	4	0
P20848	Alpha-1-antitrypsin-related protein	SERPINA2 ARGS ATR PIL SERPINA2P	Homo sapiens (human)	4	0
Q8SQG7	Hyaluronidase-2	HYAL2	Ovis aries (sheep)	4	0
C9SM62	Vacuolar protein sorting/targeting protein 10	VPS10	Verticillium alfalfae VaMs.102	4	0
Q9Z4P9	Alpha-1,6-mannanase	aman6	Niallia circulans	4	0
A5A4L1	Growth hormone secretagogue receptor type 1	GHSR	Mustela putorius furo (domestic ferret)	4	0
P99027	Large ribosomal subunit protein P2	Rplp2	Mus musculus (house mouse)	4	2
Q80X76	Serine protease inhibitor A3F	Serpina3f	Mus musculus (house mouse)	4	1
Q5I6E4	Interleukin-13	IL13	Macaca thibetana (Pere David's macaque)	4	0
A0A8D2F8D5	N-acylethanolamine-hydrolyzing acid amidase	NAAA	Theropithecus gelada (gelada)	4	0
Q8VD65	Phosphoinositide 3-kinase regulatory subunit 4	Pik3r4 Vps15	Mus musculus (house mouse)	4	2
Q3UV38	Ion transport domain-containing protein (Fragment)	Tpcn1	Mus musculus (house mouse)	4	0
A0A851AI63	Angiotensin-converting enzyme (Fragment)	Ace	Sula dactylatra	4	0

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