GlyCosmos Portal

Displaying entries **12326 - 12350** of **18496** in total

« First

‹ Prev

…

490

491

492

493

494

495

496

497

498

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q86UQ8	Transcription factor NF-E4	NFE4	0	1
Q12857	Nuclear factor 1 A-type	NFIA KIAA1439	22	2
O00712	Nuclear factor 1 B-type	NFIB	6	1
P08651	Nuclear factor 1 C-type	NFIC NFI	9	1
Q14938	Nuclear factor 1 X-type	NFIX	2	1
P19838	Nuclear factor NF-kappa-B p105 subunit	NFKB1	3	1
Q00653	Nuclear factor NF-kappa-B p100 subunit	NFKB2 LYT10	3	1
O00221	NF-kappa-B inhibitor epsilon	NFKBIE IKBE	0	1
Q9UBC1	NF-kappa-B inhibitor-like protein 1	NFKBIL1 IKBL	0	1
Q6P4R8	Nuclear factor related to kappa-B-binding protein	NFRKB INO80G	62	2
Q9Y697	Cysteine desulfurase	NFS1 NIFS	0	1
Q9UMS0	NFU1 iron-sulfur cluster scaffold homolog, mitochondrial	NFU1 HIRIP5	1	1
Q12986	Transcriptional repressor NF-X1	NFX1 NFX2	1	2
Q6ZNB6	NF-X1-type zinc finger protein NFXL1	NFXL1 OZFP	2	1
P23511	Nuclear transcription factor Y subunit alpha	NFYA	6	2
P25208	Nuclear transcription factor Y subunit beta	NFYB HAP3	0	1
Q13952	Nuclear transcription factor Y subunit gamma	NFYC	6	2
B2ZDQ1	Neutrophil gelatinase-associated lipocalin	NGAL	1	0
Q8NEJ9	Neuroguidin	NGDN C14orf120	0	1
P01138	Beta-nerve growth factor	NGF NGFB	5	1
P08138	Tumor necrosis factor receptor superfamily member 16	NGFR TNFRSF16	1	10
Q96IV0	Peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase	NGLY1 PNG1	1	1	Cogan syndrome NGLY1-deficiency Unverricht-Lundborg syndrome West syndrome alternating exotropia amyotrophic lateral sclerosis anhidrosis antithrombin III deficiency atrophic gastritis blepharospasm cancer cerebral degeneration choreatic disease cone-rod dystrophy congenital afibrinogenemia congenital ptosis corneal neovascularization corneal ulcer craniosynostosis critical illness polyneuropathy diffuse interstitial keratitis early myoclonic encephalopathy embryoma epilepsy exotropia factor V deficiency factor VII deficiency focal epilepsy focal hand dystonia fundus albipunctatus hydrocephalus hypertropia hypohidrosis inflammatory and toxic neuropathy lingual-facial-buccal dyskinesia mechanical strabismus melanoma meningoencephalitis microcephaly monocular exotropia movement disease neuropathy obsolete infantile epileptic encephalopathy obstructive sleep apnea ophthalmoplegia optic atrophy osteoporosis peripheral nervous system disease placental insufficiency polyneuropathy progressive muscular atrophy protein C deficiency protein S deficiency ptosis recurrent corneal erosion retinitis pigmentosa scoliosis skin melanoma stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability type 10 thrombophilia visual epilepsy
Q9NPE2	Neugrin	NGRN FI58G	3	0
Q9H9Q4	Non-homologous end-joining factor 1	NHEJ1 XLF	0	1
O14745	Na(+)/H(+) exchange regulatory cofactor NHE-RF1	NHERF1 NHERF SLC9A3R1	0	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements