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 **6326 - 6350** of **126547** in total

« First

‹ Prev

…

250

251

252

253

254

255

256

257

258

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
K7AUH3	Voltage-dependent L-type calcium channel subunit alpha	CACNA1C	Pan troglodytes (chimpanzee)	1	0
M9PAK3	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q4G138	LEPR protein (Fragment)	LEPR	Homo sapiens (human)	3	0
P11153	Lipoprotein lipase	LPL	Cavia porcellus (domestic guinea pig)	2	0
A0A078HP66	Xyloglucan endotransglucosylase/hydrolase	BnaA03g50060D	Brassica napus (rape)	1	0
O88797	Disabled homolog 2	Dab2 Doc2	Rattus norvegicus (Norway rat)	0	1
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
Q9GZS3	Superkiller complex protein 8	SKIC8 WDR61	Homo sapiens (human)	0	1
G5EFH6	PAW domain-containing protein	C17D12.3	Caenorhabditis elegans	2	0
Q78IQ7	Zinc transporter ZIP4	Slc39a4 Zip4	Mus musculus (house mouse)	4	0
Q8NK92	Aorsin	aorO	Aspergillus oryzae RIB40	6	0
A0A5N5MP86	Xyloglucan endotransglucosylase/hydrolase	DKX38_006890	Salix brachista	1	0
B6KHU4	Heat shock protein	BN1205_000570	Toxoplasma gondii VEG	0	1
Q9Y4I5	Tesmin	TESMIN MTL5	Homo sapiens (human)	0	1
A0A091DDR9	Hyaluronidase	H920_09983	Fukomys damarensis (Damara mole-rat)	1	0
Q9H814	Phosphorylated adapter RNA export protein	PHAX RNUXA	Homo sapiens (human)	0	1
A0A7R7DYQ7	Non-structural glycoprotein 4	NSP4	Human rotavirus A	2	0
A0A7J9KXG8	Xyloglucan endotransglucosylase/hydrolase	Goshw_011696	Gossypium schwendimanii	1	0
A0A556V6H3	Voltage-dependent L-type calcium channel subunit alpha	Baya_13132	Bagarius yarrelli (goonch)	1	0
Q646E5	Taste receptor type 2 member 8	TAS2R8	Pan paniscus (pygmy chimpanzee)	1	0
A0A0M3KL64	Hemagglutinin	HA	Influenza A virus	5	0
A0A6F9CI47	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	CSTEINMANNI_LOCUS4187772	Coregonus sp. 'balchen'	1	0
Q645Y3	Taste receptor type 2 member 41	TAS2R41	Gorilla gorilla gorilla (western lowland gorilla)	1	0
Q9NPR9	Protein GPR108	GPR108 LUSTR2	Homo sapiens (human)	10	5
Q9UQV4	Lysosome-associated membrane glycoprotein 3	LAMP3 DCLAMP TSC403	Homo sapiens (human)	9	6

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements