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 **109351 - 109375** 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
A0A9L0S8R4	N-acylethanolamine-hydrolyzing acid amidase	NAAA	Equus caballus (horse)	4	0
Q38J84	Interleukin-2 receptor subunit beta	IL2RB	Pan troglodytes (chimpanzee)	4	0
Q9R1E0	Forkhead box protein O1	Foxo1 Fkhr Foxo1a	Mus musculus (house mouse)	4	1
P28039	Acyloxyacyl hydrolase	AOAH	Homo sapiens (human)	4	5
P07759	Serine protease inhibitor A3K	Serpina3k Mcm2 Spi2	Mus musculus (house mouse)	4	10
Q0IZZ8	Beta-galactosidase 12	Os09g0539200	Oryza sativa Japonica Group (Japanese rice)	4	0
Q9SKG5	Somatic embryogenesis receptor kinase 4	SERK4 BKK1	Arabidopsis thaliana (thale cress)	4	0
Q8IZF0	Sodium leak channel NALCN	NALCN VGCNL1	Homo sapiens (human)	4	2
O95461	Xylosyl- and glucuronyltransferase LARGE1	LARGE1 KIAA0609 LARGE	Homo sapiens (human)	4	1	Axenfeld-Rieger syndrome Becker muscular dystrophy Bell's palsy Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome achondroplasia acoustic neuroma agnosia amphetamine abuse angiomatous meningioma atypical chronic myeloid leukemia, BCR-ABL1 negative 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 benign meningioma bilateral optic nerve hypoplasia blindness buphthalmos cancer cataract centronuclear myopathy cerebral convexity meningioma chronic monocytic leukemia clear cell meningioma 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 merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A6 congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism depressive disorder developmental coordination disorder diabetes mellitus dissociated nystagmus distal myopathy endomyocardial fibrosis epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial periodic paralysis fibrous meningioma fundus albipunctatus fundus dystrophy glaucoma hepatocellular carcinoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hypertropia idiopathic scoliosis imperforate anus intellectual disability intraorbital meningioma intraventricular meningioma isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly liver cancer lymphoid leukemia lymphoplasmacyte-rich meningioma major depressive disorder mechanical strabismus megaconial type congenital muscular dystrophy megalocornea melancholic depression meningioma meningocele meningothelial meningioma microcephaly microcystic meningioma microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myeloid leukemia myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia nemaline myopathy 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 melancholia obstructive hydrocephalus oculopharyngeal muscular dystrophy olfactory groove meningioma ophthalmoplegia optic atrophy parasagittal meningioma pathologic nystagmus peripheral retinal degeneration pituitary adenoma pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 psammomatous meningioma recurrent corneal erosion renal agenesis retinal detachment retinitis pigmentosa rhabdomyosarcoma rigid spine muscular dystrophy 1 rippling muscle disease 2 scoliosis secretory meningioma senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder spinal meningioma spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type transitional meningioma type 2 diabetes mellitus visual epilepsy
Q78IQ7	Zinc transporter ZIP4	Slc39a4 Zip4	Mus musculus (house mouse)	4	0
P49687	Nucleoporin NUP145	NUP145 RAT10	Saccharomyces cerevisiae S288C	4	1
Q8SPS7	Haptoglobin	HP	Sus scrofa (pig)	4	0
Q96BA8	Cyclic AMP-responsive element-binding protein 3-like protein 1	CREB3L1 OASIS	Homo sapiens (human)	4	4
O75533	Splicing factor 3B subunit 1	SF3B1 SAP155	Homo sapiens (human)	4	1
Q5U9S1	Mannose-binding protein A	MBL1 MBL-A	Sus scrofa (pig)	4	0
P23498	Osteopontin	SPP1	Gallus gallus (chicken)	4	0
P49001	Bone morphogenetic protein 2	Bmp2 Bmp-2	Rattus norvegicus (Norway rat)	4	0
Q90751	Bone morphogenetic protein 2 (Fragment)	BMP2 BMP-2	Gallus gallus (chicken)	4	0
Q5R4M0	Glutamate receptor 2	GRIA2 GLUR2 GluA2	Pongo abelii (Sumatran orangutan)	4	0
A0A1S5UZH4	Neuronal cell adhesion molecule	NRCAM	Homo sapiens (human)	4	0
Q148V7	RAB11-binding protein RELCH	Relch Kiaa1468	Mus musculus (house mouse)	4	3
Q05962	ADP/ATP translocase 1	Slc25a4 Aac1 Ant1	Rattus norvegicus (Norway rat)	4	1
Q9P0L0	Vesicle-associated membrane protein-associated protein A	VAPA VAP33	Homo sapiens (human)	4	2
Q7Z5L7	Podocan	PODN SLRR5A	Homo sapiens (human)	4	25
Q9HC58	Sodium/potassium/calcium exchanger 3	SLC24A3 NCKX3	Homo sapiens (human)	4	1

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