GlyCosmos Portal

Displaying entries **5726 - 5750** of **18496** in total

« First

‹ Prev

…

226

227

228

229

230

231

232

233

234

…

Next ›

Last »
UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
O00461	Golgi integral membrane protein 4	GOLIM4 GIMPC GOLPH4 GPP130	27	8
O00462	Beta-mannosidase	MANBA MANB1	8	13	Fabry disease allergic asthma allergic disease alternating hemiplegia of childhood angiokeratoma ascending cholangitis asthma attention deficit hyperactivity disorder autonomic neuropathy beta-mannosidosis central nervous system disease cholangitis chronic kidney disease chylomicron retention disease colorectal cancer colorectal carcinoma complement deficiency congenital nystagmus dissociated nystagmus epilepsy intellectual disability intrinsic asthma large intestine cancer learning disability lipid storage disease lysosomal storage disease multiple sclerosis nervous system disease obsolete constipation pathologic nystagmus primary biliary cholangitis primary sclerosing cholangitis sarcoidosis sclerosing cholangitis sensorineural hearing loss speech disorder spontaneous ocular nystagmus suppurative cholangitis uveoparotid fever visual epilepsy
O00468	Agrin	AGRN AGRIN	58	124	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Bell's palsy Pick's disease Reye syndrome acute myeloid leukemia agnosia cancer central sleep apnea cerebral degeneration congenital myasthenic syndrome 10 congenital myasthenic syndrome 8 congenital myasthenic syndrome congenital nystagmus congenital ptosis critical illness polyneuropathy developmental coordination disorder dissociated nystagmus embryoma epilepsy esophagitis esotropia facial nerve disease facial paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome gastroesophageal reflux disease intellectual disability learning disability lung adenocarcinoma lung cancer monocular esotropia obstructive sleep apnea ophthalmoplegia papillary adenocarcinoma papillary renal cell carcinoma pathologic nystagmus peptic esophagitis polyhydramnios polyneuropathy progressive bulbar palsy ptosis scoliosis sensorineural hearing loss spontaneous ocular nystagmus thyroid gland papillary carcinoma visual epilepsy
O00469	Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2	PLOD2	9	45	Bruck syndrome
O00470	Homeobox protein Meis1	MEIS1	1	1
O00471	Exocyst complex component 5	EXOC5 SEC10 SEC10L1	0	1
O00472	RNA polymerase II elongation factor ELL2	ELL2	1	3
O00476	Sodium-dependent phosphate transport protein 4	SLC17A3 NPT4	4	0
O00478	Butyrophilin subfamily 3 member A3	BTN3A3 BTF3	1	1
O00479	High mobility group nucleosome-binding domain-containing protein 4	HMGN4 HMG17L3 NHC	0	1
O00481	Butyrophilin subfamily 3 member A1	BTN3A1 BTF5	3	1
O00483	Cytochrome c oxidase subunit NDUFA4	NDUFA4	0	1
O00487	26S proteasome non-ATPase regulatory subunit 14	PSMD14 POH1	1	2
O00488	Zinc finger protein 593	ZNF593 ZT86	0	1
O00499	Myc box-dependent-interacting protein 1	BIN1 AMPHL	2	1
O00505	Importin subunit alpha-4	KPNA3 QIP2	0	1
O00506	Serine/threonine-protein kinase 25	STK25 SOK1 YSK1	0	1
O00507	Ubiquitin carboxyl-terminal hydrolase 9Y	USP9Y DFFRY	1	1
O00512	B-cell CLL/lymphoma 9 protein	BCL9	2	1
O00519	Fatty-acid amide hydrolase 1	FAAH FAAH1	0	1
O00526	Uroplakin-2	UPK2	3	0
O00533	Neural cell adhesion molecule L1-like protein	CHL1 CALL	17	21
O00541	Pescadillo homolog	PES1	0	1
O00548	Delta-like protein 1	DLL1	2	1
O00555	Voltage-dependent P/Q-type calcium channel subunit alpha-1A	CACNA1A CACH4 CACN3 CACNL1A4	1	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements