GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q6NVV3	Magnesium transporter NIPA3	NIPAL1 NIPA3 NPAL1	4	0
Q9Y2I6	Ninein-like protein	NINL KIAA0980 NLP	0	1
Q92982	Ninjurin-1	NINJ1	1	0
Q8N4C6	Ninein	NIN KIAA1565	6	1
Q8IY84	Serine/threonine-protein kinase NIM1	NIM1K NIM1	0	1
Q9BYG3	MKI67 FHA domain-interacting nucleolar phosphoprotein	NIFK MKI67IP NOPP34	0	1
Q14112	Nidogen-2	NID2	37	115
P14543	Nidogen-1	NID1 NID	19	7
Q5BLP8	NELL2-interacting cell ontogeny regulator 1	NICOL1 C4orf48	1	1
Q86XR2	Protein Niban 3	NIBAN3 BCNP1 FAM129C	0	1
Q96TA1	Protein Niban 2	NIBAN2 C9orf88 FAM129B	2	1
Q9BZQ8	Protein Niban 1	NIBAN1 C1orf24 FAM129A NIBAN	1	2
Q5HYW2	NHS-like protein 2	NHSL2	0	1
Q5SYE7	NHS-like protein 1	NHSL1 C6orf63 KIAA1357	3	1
Q6T4R5	Actin remodeling regulator NHS	NHS	3	3
Q9NX24	H/ACA ribonucleoprotein complex subunit 2	NHP2 NOLA2	0	1
Q5JS37	NHL repeat-containing protein 3	NHLRC3	5	7
Q8NBF2	NHL repeat-containing protein 2	NHLRC2	1	1
Q6VVB1	E3 ubiquitin-protein ligase NHLRC1	NHLRC1 EPM2B	1	1
Q02575	Helix-loop-helix protein 1	NHLH1 BHLHA35 HEN1	0	1
Q15599	Na(+)/H(+) exchange regulatory cofactor NHE-RF2	NHERF2 SLC9A3R2	0	1
O14745	Na(+)/H(+) exchange regulatory cofactor NHE-RF1	NHERF1 NHERF SLC9A3R1	0	1
Q9H9Q4	Non-homologous end-joining factor 1	NHEJ1 XLF	0	1
Q9NPE2	Neugrin	NGRN FI58G	3	0
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

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