GlyCosmos Portal

GlyCosmos Glycoproteins

Integrated list of glycoproteins extracted from UniProt and annotated with glycosylation data from GlyGen, GlyConnect, GlycoProtDB and The O-GlcNAc Database. For each entry, information such as glycosylation site, glycans, diseases, 3D structures, and pathway information are available.

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 **116151 - 116175** 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
P12556	Hemagglutinin-neuraminidase	HN	Newcastle disease virus strain Italien/45	6	0
P21303	Merozoite receptor PK66	PK66	Plasmodium knowlesi strain Nuri	6	0
Q63515	C4b-binding protein beta chain	C4bpb	Rattus norvegicus (Norway rat)	6	0
Q5R530	Neurexophilin-1	NXPH1	Pongo abelii (Sumatran orangutan)	6	0
Q96PB7	Noelin-3	OLFM3 NOE3	Homo sapiens (human)	6	1
A0A7D3QMB1	Pre-glycoprotein polyprotein GP complex	GPC	Mammarenavirus tacaribeense	6	0
H9XC94	Hemagglutinin	HA	Influenza A virus (A/Hong Kong/1/1968(H3N2))	6	0
Q12232	Uncharacterized protein SLP1	SLP1	Saccharomyces cerevisiae S288C	6	0
P12824	Envelope glycoprotein H	gH UL75	Human herpesvirus 5 strain AD169	6	0
O77802	Angiopoietin-2	ANGPT2 ANG2	Bos taurus (cattle)	6	0
Q95149	Kappa-casein (Fragment)	CSN3 CSN10 CSNK	Cervus elaphus (red deer)	6	0
B2KWH4	ABC transporter 1	ABC1	Histoplasma capsulatum	6	0
P05156	Complement factor I	CFI IF	Homo sapiens (human)	6	85
Q20176	Zinc metalloproteinase nas-39	nas-39	Caenorhabditis elegans	6	0
Q75V66	Anoctamin-5	ANO5 GDD1 TMEM16E	Homo sapiens (human)	6	0
P56715	Oxygen-regulated protein 1	RP1 ORP1	Homo sapiens (human)	6	1
Q26307	Protein anachronism	ana	Drosophila melanogaster (fruit fly)	6	0
Q9Z2Y9	Klotho	Kl	Rattus norvegicus (Norway rat)	6	0
Q80VM5	Dipeptidyl aminopeptidase-like protein 6	Dpp6	Mus musculus (house mouse)	6	0
Q9UKY4	Protein O-mannosyl-transferase 2	POMT2	Homo sapiens (human)	6	10	Axenfeld-Rieger syndrome Bell's palsy Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome X-linked dilated cardiomyopathy 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 buphthalmos campomelic dysplasia cancer cataract cleft lip cleft palate coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cone-rod dystrophy congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A2 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome craniometaphyseal dysplasia cryptorchidism cystic kidney disease developmental coordination disorder dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy distal myopathy embryoma epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fundus albipunctatus glaucoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hyperopia hypertropia imperforate anus intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly mechanical strabismus megalocornea meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia 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 ophthalmoplegia optic atrophy peripheral retinal degeneration pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion renal agenesis retinal detachment retinitis pigmentosa rippling muscle disease 2 scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus speech disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type tuberous sclerosis visual epilepsy
Q6NXV8	receptor protein-tyrosine kinase	Csf1r	Mus musculus (house mouse)	6	0
Q40161	Polygalacturonase-1 non-catalytic subunit beta	GP1	Solanum lycopersicum (tomato)	6	0
P41731	CD63 antigen	Cd63	Mus musculus (house mouse)	6	3
Q75UR0	Anoctamin-5	Ano5 Gdd1 Tmem16e	Mus musculus (house mouse)	6	0
P14873	Microtubule-associated protein 1B	Map1b Mtap1b Mtap5	Mus musculus (house mouse)	6	1

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