GlyCosmos Portal

Displaying entries **2726 - 2750** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
P23381	Tryptophan--tRNA ligase, cytoplasmic	WARS1 IFI53 WARS WRS	1	2
O00161	Synaptosomal-associated protein 23	SNAP23	1	2
O43155	Leucine-rich repeat transmembrane protein FLRT2	FLRT2 KIAA0405	5	2
Q8NHV4	Protein NEDD1	NEDD1	5	2
Q969X6	U3 small nucleolar RNA-associated protein 4 homolog	UTP4 CIRH1A KIAA1988 cPERP-E	1	2
O75084	Frizzled-7	FZD7	5	2
O60925	Prefoldin subunit 1	PFDN1 PFD1	2	2
P40925	Malate dehydrogenase, cytoplasmic	MDH1 MDHA	2	2	Creutzfeldt-Jakob disease Gerstmann-Straussler-Scheinker syndrome X-linked dilated cardiomyopathy adult respiratory distress syndrome amyotrophic lateral sclerosis cancer cone-rod dystrophy dilated cardiomyopathy 1A 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 embryoma fatal familial insomnia fundus albipunctatus lung cancer lung non-small cell carcinoma microphthalmia newborn respiratory distress syndrome obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma progressive muscular atrophy retinitis pigmentosa schizophrenia
Q5T0W9	Protein FAM83B	FAM83B C6orf143	2	2
Q09161	Nuclear cap-binding protein subunit 1	NCBP1 CBP80 NCBP	3	2
P36551	Oxygen-dependent coproporphyrinogen-III oxidase, mitochondrial	CPOX CPO CPX	1	2
Q13315	Serine-protein kinase ATM	ATM	5	2
Q8IVF2	Protein AHNAK2	AHNAK2 C14orf78 KIAA2019	28	2
Q96PU5	E3 ubiquitin-protein ligase NEDD4-like	NEDD4L KIAA0439 NEDL3	2	2
Q92540	Nonsense-mediated mRNA decay factor SMG7	SMG7 C1orf16 EST1C KIAA0250	4	2
P61019	Ras-related protein Rab-2A	RAB2A RAB2	2	2
Q14999	Cullin-7	CUL7 KIAA0076	1	2
O60292	Signal-induced proliferation-associated 1-like protein 3	SIPA1L3 KIAA0545 SPAL3	2	2
O43424	Glutamate receptor ionotropic, delta-2	GRID2 GLURD2	4	2
Q9UNP4	Lactosylceramide alpha-2,3-sialyltransferase	ST3GAL5 SIAT9	3	2	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome Niemann-Pick disease type C1 Niemann-Pick disease Rett syndrome SPOAN syndrome Troyer syndrome Unverricht-Lundborg syndrome agnosia arthritis arthropathy blepharospasm blindness cerebral palsy congenital nystagmus developmental and epileptic encephalopathy 36 dissociated nystagmus dystonia early myoclonic encephalopathy endocrine exophthalmos focal hand dystonia hemiplegia hepatocellular carcinoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer locked-in syndrome microcephaly optic atrophy paroxysmal nonkinesigenic dyskinesia 1 paroxysmal nonkinesigenic dyskinesia 2 pathologic nystagmus quadriplegia salt and pepper syndrome sensorineural hearing loss spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spontaneous ocular nystagmus status epilepticus stereotypic movement disorder syndromic X-linked intellectual disability 94 thromboangiitis obliterans trichohepatoenteric syndrome 1 trichohepatoenteric syndrome visual epilepsy
Q9Y694	Solute carrier family 22 member 7	SLC22A7 NLT OAT2	2	2
P17066	Heat shock 70 kDa protein 6	HSPA6 HSP70B'	4	2
Q9NYF8	Bcl-2-associated transcription factor 1	BCLAF1 BTF KIAA0164	11	2
Q9BQC3	2-(3-amino-3-carboxypropyl)histidine synthase subunit 2	DPH2 DPH2L2	4	2
Q00341	Vigilin	HDLBP HBP VGL	2	2

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