GlyCosmos Portal

Displaying entries **16751 - 16775** of **18496** in total

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9NRH1	Protein YAE1 homolog	YAE1 C7orf36 YAE1D1	0	1
Q9NRH2	SNF-related serine/threonine-protein kinase	SNRK KIAA0096 SNFRK	2	1
Q9NRH3	Tubulin gamma-2 chain	TUBG2	0	1
Q9NRJ3	C-C motif chemokine 28	CCL28 SCYA28	1	0
Q9NRJ4	Tubby-related protein 4	TULP4 KIAA1397 TUBL4 TUSP	2	1
Q9NRJ7	Protocadherin beta-16	PCDHB16 KIAA1621 PCDH3X	4	2
Q9NRK6	ATP-binding cassette sub-family B member 10, mitochondrial	ABCB10	1	1
Q9NRL2	Bromodomain adjacent to zinc finger domain protein 1A	BAZ1A ACF1 WCRF180	2	1
Q9NRL3	Striatin-4	STRN4 ZIN	2	1
Q9NRM0	Solute carrier family 2, facilitated glucose transporter member 9	SLC2A9 GLUT9	1	0
Q9NRM1	Enamelin	ENAM	10	0
Q9NRM2	Zinc finger protein 277	ZNF277 NRIF4 ZNF277P	1	1
Q9NRM6	Interleukin-17 receptor B	IL17RB CRL4 EVI27 IL17BR	6	8
Q9NRM7	Serine/threonine-protein kinase LATS2	LATS2 KPM	8	1
Q9NRN5	Olfactomedin-like protein 3	OLFML3	3	105
Q9NRN7	L-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase	AASDHPPT	0	1
Q9NRP0	Oligosaccharyltransferase complex subunit OSTC	OSTC	0	1
Q9NRP2	COX assembly mitochondrial protein 2 homolog	CMC2 C16orf61	0	1
Q9NRR2	Tryptase gamma	TPSG1 PRSS31 TMT	1	1
Q9NRR5	Ubiquilin-4	UBQLN4 C1orf6 CIP75 UBIN	2	2
Q9NRR6	Phosphatidylinositol polyphosphate 5-phosphatase type IV	INPP5E	0	1	Bannayan-Riley-Ruvalcaba syndrome Bardet-Biedl syndrome 10 Bardet-Biedl syndrome 11 Bardet-Biedl syndrome 12 Bardet-Biedl syndrome 13 Bardet-Biedl syndrome 14 Bardet-Biedl syndrome 15 Bardet-Biedl syndrome 16 Bardet-Biedl syndrome 17 Bardet-Biedl syndrome 18 Bardet-Biedl syndrome 19 Bardet-Biedl syndrome 1 Bardet-Biedl syndrome 2 Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 4 Bardet-Biedl syndrome 5 Bardet-Biedl syndrome 6 Bardet-Biedl syndrome 7 Bardet-Biedl syndrome 8 Bardet-Biedl syndrome 9 Bardet-Biedl syndrome Cogan syndrome Hirschsprung's disease Joubert syndrome 1 Joubert syndrome Kartagener syndrome Klippel-Feil syndrome Laurence-Moon syndrome Meckel syndrome 1 Meckel syndrome adult medulloblastoma autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease blindness cancer cataract central sleep apnea childhood medulloblastoma cleft palate clubfoot coloboma of optic nerve coloboma communicating hydrocephalus congenital nystagmus congenital ptosis cystic kidney disease dextrocardia diffuse interstitial keratitis dissociated nystagmus embryoma epilepsy episodic kinesigenic dyskinesia 1 fundus dystrophy glomerulonephritis hepatocellular carcinoma hydrocephalus hypertropia inguinal hernia intellectual disability interstitial lung disease isolated cleft palate kidney disease kidney failure learning disability leukoplakia of penis liver cancer liver cirrhosis mechanical strabismus medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma nephritis nephrosis non-congenital cyst of kidney obesity obstructive hydrocephalus oculocerebrorenal syndrome ophthalmoplegia patent ductus arteriosus pathologic nystagmus polycystic kidney disease 4 polydactyly portal hypertension primary ciliary dyskinesia 1 primary ciliary dyskinesia ptosis pyoureter scoliosis senile degeneration of brain skin melanoma spondylolisthesis spontaneous ocular nystagmus strabismus viral infectious disease visual epilepsy visual pathway disease
Q9NRR8	CDC42 small effector protein 1	CDC42SE1 SPEC1	0	1
Q9NRS4	Transmembrane protease serine 4	TMPRSS4 TMPRSS3	2	0
Q9NRV9	Heme-binding protein 1	HEBP1 HBP	0	1
Q9NRW1	Ras-related protein Rab-6B	RAB6B	0	1

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