GlyCosmos Portal

Displaying entries **5901 - 5925** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q96P11	28S rRNA (cytosine-C(5))-methyltransferase	NSUN5 NSUN5A WBSCR20 WBSCR20A	0	1
Q08J23	RNA cytosine C(5)-methyltransferase NSUN2	NSUN2 SAKI TRM4	2	3
Q9H0G5	Nuclear speckle splicing regulatory protein 1	NSRP1 CCDC55 NSRP70	0	1
Q6X4W1	NMDA receptor synaptonuclear signaling and neuronal migration factor	NSMF NELF	1	1
Q9NXX6	Non-structural maintenance of chromosomes element 4 homolog A	NSMCE4A C10orf86	1	1
Q96MF7	E3 SUMO-protein ligase NSE2	NSMCE2 C8orf36 MMS21	0	1
Q92636	Protein FAN	NSMAF FAN	0	1
Q96IY1	Kinetochore-associated protein NSL1 homolog	NSL1 C1orf48	0	1
Q9Y328	Neuronal vesicle trafficking-associated protein 2	NSG2 CALY3	0	1
P42857	Neuronal vesicle trafficking-associated protein 1	NSG1 D4S234 NEEP21	4	1
Q9UNZ2	NSFL1 cofactor p47	NSFL1C UBXN2C	0	1
P46459	Vesicle-fusing ATPase	NSF	0	1
Q15738	Sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating	NSDHL H105E3	0	1	Bloch-Sulzberger syndrome Joubert syndrome Miller-Dieker lissencephaly syndrome Potter's syndrome Sjogren-Larsson syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 acquired hyperkeratosis autosomal dominant chondrodysplasia punctata autosomal recessive congenital ichthyosis bilateral renal aplasia chondrodysplasia punctata cleft lip complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cutaneous fibrous histiocytoma epidermal nevus epilepsy granuloma annulare head and neck squamous cell carcinoma heart septal defect hidradenoma hydranencephaly hydronephrosis hypertropia hypomelanosis of Ito intellectual disability learning disability lissencephaly mechanical strabismus microcephaly obsolete congenital ichthyosiform erythroderma omphalocele ophthalmoplegia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin papilloma skin tag strabismus syndromic X-linked intellectual disability Najm type syringoma umbilical hernia ventricular septal defect verruciform xanthoma of skin visual epilepsy
Q9BZ95	Histone-lysine N-methyltransferase NSD3	NSD3 WHSC1L1	4	4
O96028	Histone-lysine N-methyltransferase NSD2	NSD2 KIAA1090 MMSET TRX5 WHSC1	4	1
Q96L73	Histone-lysine N-methyltransferase, H3 lysine-36 specific	NSD1 ARA267 KMT3B	2	1
Q9HDB5	Neurexin-3-beta	NRXN3 KIAA0743	4	0
Q9Y4C0	Neurexin-3	NRXN3 C14orf60 KIAA0743	7	0
P58401	Neurexin-2-beta	NRXN2	2	0
Q9P2S2	Neurexin-2	NRXN2 KIAA0921	8	5
P58400	Neurexin-1-beta	NRXN1	2	0
Q9ULB1	Neurexin-1	NRXN1 KIAA0578	6	6
Q86YC3	Transforming growth factor beta activator LRRC33	NRROS LRRC33	11	5
X5D7M1	Neuropilin 2 isoform B (Fragment)	NRP2	2	0
B7ZL68	Neuropilin	NRP2	2	0

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