GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4426 - 4450** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
25836	NIPBL cohesin loading factor	NIPBL
348938	NIPA like domain containing 4	NIPAL4
57185	NIPA like domain containing 3	NIPAL3
79815	NIPA like domain containing 2	NIPAL2
152519	NIPA like domain containing 1	NIPAL1
4814	ninjurin 1	NINJ1
51199	ninein	NIN
167359	NIM1 serine/threonine protein kinase	NIM1K
84365	nucleolar protein interacting with the FHA domain of MKI67	NIFK
22795	nidogen 2	NID2
4811	nidogen 1	NID1
64855	niban apoptosis regulator 2	NIBAN2
116496	niban apoptosis regulator 1	NIBAN1
340527	NHS like 2	NHSL2
57224	NHS like 1	NHSL1
4810	NHS actin remodeling regulator	NHS
387921	NHL repeat containing 3	NHLRC3
374354	NHL repeat containing 2	NHLRC2
378884	NHL repeat containing E3 ubiquitin protein ligase 1	NHLRC1	Lafora disease
51335	neugrin, neurite outgrowth associated	NGRN
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
4804	nerve growth factor receptor	NGFR
4803	nerve growth factor	NGF
4802	nuclear transcription factor Y subunit gamma	NFYC
4800	nuclear transcription factor Y subunit alpha	NFYA

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