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 **151 - 175** 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
A0A193AH98	Matrix protein 2	M2 M	Influenza A virus (A/Arizona/53/2015(H3N2))	1	0
A0A7L3NFT0	PANX3 protein (Fragment)	Panx3	Oreotrochilus melanogaster	1	0
A0A075SLD6	Matrix protein 2	M2 M	Influenza A virus (A/Singapore/H2013.721a/2013(H3N2))	1	0
G5AE35	Glucanase inhibitor protein 3	GIP3	Phytophthora sojae strain P6497	1	0
M9PA20	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
P08603	Complement factor H	CFH HF HF1 HF2	Homo sapiens (human)	10	140
O43808	Peroxisomal membrane protein PMP34	SLC25A17 PMP34	Homo sapiens (human)	0	1
I3JZD2	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	B3GAT1	Oreochromis niloticus (Nile tilapia)	1	0
L0MSB3	Matrix protein 2	M2 M	Influenza A virus (A/swine/Ohio/09SW83M/2009(H3N2))	1	0
A0A452THM5	Voltage-dependent P/Q-type calcium channel subunit alpha	CACNA1A	Ursus maritimus (polar bear)	1	0
A0A8X7X2K8	Hyaluronidase (Fragment)	Hyal4	Polypterus senegalus (gray bichir)	1	0
Q3TSW6	L-selectin	Sell	Mus musculus (house mouse)	6	0
Q5NTB3	Coagulation factor XI	F11	Bos taurus (cattle)	4	0
Q4DJF1	High-temperature-induced dauer-formation protein	Tc00.1047053507991.80	Trypanosoma cruzi strain CL Brener	0	1
A0A2H8TJQ4	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase (Fragment)	GlcAT-S_0	Melanaphis sacchari	1	0
P28106	Protein Wnt-7b (Fragment)	WNT-7B	Alopias vulpinus (thresher shark)	1	0
A0A2H4ZEQ2	Non-structural glycoprotein 4	NSP4	Rotavirus A	2	0
Q01320	DNA topoisomerase 2-alpha	Top2a Top-2 Top2	Mus musculus (house mouse)	1	2
A0A097F4Q1	Pre-glycoprotein polyprotein GP complex	GPC	Mammarenavirus lassaense	11	0
A1YL82	Agouti-signaling protein	ASIP	Leontopithecus rosalia (golden lion tamarin)	1	0
V5AUM3	Methyltransferase type 11 domain-containing protein	TCDM_07419	Trypanosoma cruzi Dm28c	0	1
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
Q9W6T7	Presenilin-1	psen1	Danio rerio (zebrafish)	0	1
Q09991	Serine carboxypeptidase ctsa-4.1	ctsa-4.1 ctsa-1 drd-7	Caenorhabditis elegans	3	0
A0A096MWA1	Pannexin	PANX1 PANX	Papio anubis (olive baboon)	1	0

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