GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **1726 - 1750** of **18496** in total

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UniProt ID ▼	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9NRR6	Phosphatidylinositol polyphosphate 5-phosphatase type IV	INPP5E	Homo sapiens (human)	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
Q9NRR5	Ubiquilin-4	UBQLN4 C1orf6 CIP75 UBIN	Homo sapiens (human)	2	2
Q9NRR2	Tryptase gamma	TPSG1 PRSS31 TMT	Homo sapiens (human)	1	1
Q9NRP2	COX assembly mitochondrial protein 2 homolog	CMC2 C16orf61	Homo sapiens (human)	0	1
Q9NRP0	Oligosaccharyltransferase complex subunit OSTC	OSTC	Homo sapiens (human)	0	1
Q9NRN7	L-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase	AASDHPPT	Homo sapiens (human)	0	1
Q9NRN5	Olfactomedin-like protein 3	OLFML3	Homo sapiens (human)	3	105
Q9NRM7	Serine/threonine-protein kinase LATS2	LATS2 KPM	Homo sapiens (human)	8	1
Q9NRM6	Interleukin-17 receptor B	IL17RB CRL4 EVI27 IL17BR	Homo sapiens (human)	6	8
Q9NRM2	Zinc finger protein 277	ZNF277 NRIF4 ZNF277P	Homo sapiens (human)	1	1
Q9NRM1	Enamelin	ENAM	Homo sapiens (human)	10	0
Q9NRM0	Solute carrier family 2, facilitated glucose transporter member 9	SLC2A9 GLUT9	Homo sapiens (human)	1	0
Q9NRL3	Striatin-4	STRN4 ZIN	Homo sapiens (human)	2	1
Q9NRL2	Bromodomain adjacent to zinc finger domain protein 1A	BAZ1A ACF1 WCRF180	Homo sapiens (human)	2	1
Q9NRK6	ATP-binding cassette sub-family B member 10, mitochondrial	ABCB10	Homo sapiens (human)	1	1
Q9NRJ7	Protocadherin beta-16	PCDHB16 KIAA1621 PCDH3X	Homo sapiens (human)	4	2
Q9NRJ4	Tubby-related protein 4	TULP4 KIAA1397 TUBL4 TUSP	Homo sapiens (human)	2	1
Q9NRJ3	C-C motif chemokine 28	CCL28 SCYA28	Homo sapiens (human)	1	0
Q9NRH3	Tubulin gamma-2 chain	TUBG2	Homo sapiens (human)	0	1
Q9NRH2	SNF-related serine/threonine-protein kinase	SNRK KIAA0096 SNFRK	Homo sapiens (human)	2	1
Q9NRH1	Protein YAE1 homolog	YAE1 C7orf36 YAE1D1	Homo sapiens (human)	0	1
Q9NRG9	Aladin	AAAS ADRACALA	Homo sapiens (human)	2	1
Q9NRG4	N-lysine methyltransferase SMYD2	SMYD2 KMT3C	Homo sapiens (human)	0	1
Q9NRG0	Chromatin accessibility complex protein 1	CHRAC1 CHRAC15	Homo sapiens (human)	0	1
Q9NRF9	DNA polymerase epsilon subunit 3	POLE3 CHRAC17	Homo sapiens (human)	1	2

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