GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **5526 - 5550** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
4779	NFE2 like bZIP transcription factor 1	NFE2L1
4780	NFE2 like bZIP transcription factor 2	NFE2L2
4774	nuclear factor I A	NFIA
4781	nuclear factor I B	NFIB
4782	nuclear factor I C	NFIC
4784	nuclear factor I X	NFIX
4790	nuclear factor kappa B subunit 1	NFKB1
4791	nuclear factor kappa B subunit 2	NFKB2
4798	nuclear factor related to kappaB binding protein	NFRKB
9054	NFS1 cysteine desulfurase	NFS1
27247	NFU1 iron-sulfur cluster scaffold	NFU1
4799	nuclear transcription factor, X-box binding 1	NFX1
152518	nuclear transcription factor, X-box binding like 1	NFXL1
4800	nuclear transcription factor Y subunit alpha	NFYA
4802	nuclear transcription factor Y subunit gamma	NFYC
4803	nerve growth factor	NGF
4804	nerve growth factor receptor	NGFR
55768	N-glycanase 1	NGLY1 FLJ11005 PNG-1 PNG1 peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase peptide:N-glycanase	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
51335	neugrin, neurite outgrowth associated	NGRN
378884	NHL repeat containing E3 ubiquitin protein ligase 1	NHLRC1	Lafora disease
374354	NHL repeat containing 2	NHLRC2
387921	NHL repeat containing 3	NHLRC3
4810	NHS actin remodeling regulator	NHS
57224	NHS like 1	NHSL1
340527	NHS like 2	NHSL2

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