GlyCosmos Portal

Displaying entries **12576 - 12600** of **18496** in total

« First

‹ Prev

…

500

501

502

503

504

505

506

507

508

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P58400	Neurexin-1-beta	NRXN1	2	0
Q9P2S2	Neurexin-2	NRXN2 KIAA0921	8	5
P58401	Neurexin-2-beta	NRXN2	2	0
Q9Y4C0	Neurexin-3	NRXN3 C14orf60 KIAA0743	7	0
Q9HDB5	Neurexin-3-beta	NRXN3 KIAA0743	4	0
Q96L73	Histone-lysine N-methyltransferase, H3 lysine-36 specific	NSD1 ARA267 KMT3B	2	1
O96028	Histone-lysine N-methyltransferase NSD2	NSD2 KIAA1090 MMSET TRX5 WHSC1	4	1
Q9BZ95	Histone-lysine N-methyltransferase NSD3	NSD3 WHSC1L1	4	4
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
P46459	Vesicle-fusing ATPase	NSF	0	1
Q9UNZ2	NSFL1 cofactor p47	NSFL1C UBXN2C	0	1
P42857	Neuronal vesicle trafficking-associated protein 1	NSG1 D4S234 NEEP21	4	1
Q9Y328	Neuronal vesicle trafficking-associated protein 2	NSG2 CALY3	0	1
Q96IY1	Kinetochore-associated protein NSL1 homolog	NSL1 C1orf48	0	1
Q92636	Protein FAN	NSMAF FAN	0	1
Q96MF7	E3 SUMO-protein ligase NSE2	NSMCE2 C8orf36 MMS21	0	1
Q9NXX6	Non-structural maintenance of chromosomes element 4 homolog A	NSMCE4A C10orf86	1	1
Q6X4W1	NMDA receptor synaptonuclear signaling and neuronal migration factor	NSMF NELF	1	1
Q9H0G5	Nuclear speckle splicing regulatory protein 1	NSRP1 CCDC55 NSRP70	0	1
Q08J23	RNA cytosine C(5)-methyltransferase NSUN2	NSUN2 SAKI TRM4	2	3
Q96P11	28S rRNA (cytosine-C(5))-methyltransferase	NSUN5 NSUN5A WBSCR20 WBSCR20A	0	1
Q8NE18	Putative methyltransferase NSUN7	NSUN7	1	1
P49902	Cytosolic purine 5'-nucleotidase	NT5C2 NT5B NT5CP PNT5	0	1
Q9H0P0	Cytosolic 5'-nucleotidase 3A	NT5C3A NT5C3 P5N1 UMPH1	0	1
Q969T7	7-methylguanosine phosphate-specific 5'-nucleotidase	NT5C3B NT5C3L	0	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements