GlyCosmos Portal

Displaying entries **4001 - 4025** of **18496** in total

« First

‹ Prev

…

157

158

159

160

161

162

163

164

165

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q86U70	LIM domain-binding protein 1	LDB1 CLIM2	3	1
Q9P242	Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 2	NYAP2 KIAA1486	1	1
Q7Z6K4	Notch-regulated ankyrin repeat-containing protein	NRARP	1	1
Q8WVV4	Protein POF1B	POF1B	0	1
Q9P212	1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase epsilon-1	PLCE1 KIAA1516 PLCE PPLC	3	1	46,XY sex reversal Alzheimer's disease Barrett's esophagus Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Japanese encephalitis Miller-Dieker lissencephaly syndrome West Nile fever acute myeloid leukemia adenocarcinoma adenoma adenosarcoma agenesis of the corpus callosum with peripheral neuropathy atrophic gastritis bladder carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease chromosome 17p13.1 deletion syndrome chronic kidney disease chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma common wart congestive heart failure cribriform carcinoma cytochrome-c oxidase deficiency disease dengue disease dengue hemorrhagic fever embryoma esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia familial nephrotic syndrome focal segmental glomerulosclerosis gallbladder cancer gallbladder carcinoma gastric adenocarcinoma gastric cardia adenocarcinoma gastric cardia carcinoma gastritis gastroesophageal reflux disease gastrointestinal system cancer glomerulonephritis granular cell carcinoma head and neck squamous cell carcinoma heart disease hepatitis B hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hypertension large intestine cancer lipoid nephrosis lissencephaly liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma migraine mitochondrial metabolism disease motor peripheral neuropathy myelodysplastic syndrome nephritis nephroblastoma nephrotic syndrome type 1 nephrotic syndrome type 2 nephrotic syndrome type 3 nephrotic syndrome obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum open-angle glaucoma peptic esophagitis primary open angle glaucoma proteinuria sarcomatoid carcinoma squamous cell carcinoma squamous cell neoplasm stomach cancer stomach carcinoma temporal arteritis tongue squamous cell carcinoma tubular adenocarcinoma urinary bladder cancer viral infectious disease yellow fever
Q9H8Y5	tRNA endonuclease ANKZF1	ANKZF1 ZNF744	1	1
Q9BQS2	Synaptotagmin-15	SYT15	0	1
Q6ZS27	Zinc finger protein 662	ZNF662	0	1
Q9Y3B8	Oligoribonuclease, mitochondrial	REXO2 SFN SMFN	0	1
Q14590	Zinc finger protein 235	ZNF235 ZFP93 ZNF270	0	1
Q9Y3D8	Adenylate kinase isoenzyme 6	AK6 CINAP	0	1
Q9ULS5	Transmembrane and coiled-coil domain protein 3	TMCC3 KIAA1145	0	1
P0CG13	Chromosome transmission fidelity protein 8 homolog	CHTF8 CTF8	3	1
Q9BVA0	Katanin p80 WD40 repeat-containing subunit B1	KATNB1	1	1
O60682	Musculin	MSC ABF1 BHLHA22	0	1
O75676	Ribosomal protein S6 kinase alpha-4	RPS6KA4 MSK2	0	1
P28347	Transcriptional enhancer factor TEF-1	TEAD1 TCF13 TEF1	3	1
Q5MNZ9	WD repeat domain phosphoinositide-interacting protein 1	WIPI1 WIPI49	6	1
Q9BXR0	Queuine tRNA-ribosyltransferase catalytic subunit 1	QTRT1 TGT TGUT	0	1	IgA glomerulonephritis acute pancreatitis breast cancer bronchus cancer bronchus carcinoma cancer carcinoma cerebral infarction cerebrovascular disease essential thrombocythemia functionless pituitary adenoma hepatocellular carcinoma liver angiosarcoma liver cancer lung benign neoplasm lung cancer lung carcinoma multiple sclerosis myotonic dystrophy type 2 pancreatitis parapsoriasis parietal foramina prolactinoma psoriasis pulmonary embolism pustulosis of palm and sole sarcomatoid carcinoma split hand-foot malformation 1 split hand-foot malformation 2 split hand-foot malformation 3 split hand-foot malformation 4 split hand-foot malformation 5 split hand-foot malformation 6 split hand-foot malformation
Q9P2K6	Kelch-like protein 42	KLHL42 KIAA1340 KLHDC5	1	1
A1L188	NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 8	NDUFAF8 C17orf89	1	1
Q5JR12	Protein phosphatase 1J	PPM1J PPP2CZ	0	1
Q99547	M-phase phosphoprotein 6	MPHOSPH6 MPP6	0	1
Q9Y262	Eukaryotic translation initiation factor 3 subunit L	EIF3L EIF3EIP EIF3S6IP	0	1
Q4VC05	B-cell CLL/lymphoma 7 protein family member A	BCL7A	0	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements