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 **14951 - 14975** 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
Q8N5M4	Tetratricopeptide repeat protein 9C	TTC9C	Homo sapiens (human)	0	1
P78346	Ribonuclease P protein subunit p30	RPP30 RNASEP2	Homo sapiens (human)	0	1
Q9UNZ2	NSFL1 cofactor p47	NSFL1C UBXN2C	Homo sapiens (human)	0	1
P53597	Succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial	SUCLG1	Homo sapiens (human)	1	1	Leigh disease McCune Albright syndrome brain disease cardiomyopathy central nervous system cancer cerebral degeneration endomyocardial fibrosis epilepsy familial hypertrophic cardiomyopathy giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hypertrophic cardiomyopathy hypoglycemia hypophosphatemia intellectual disability lactic acidosis learning disability methylmalonic acidemia mitochondrial DNA depletion syndrome 5 mitochondrial DNA depletion syndrome 9 mitochondrial DNA depletion syndrome mitochondrial encephalomyopathy mixed glioma skin disease stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 visual epilepsy
P57772	Selenocysteine-specific elongation factor	EEFSEC SELB	Homo sapiens (human)	0	1
P13533	Myosin-6	MYH6 MYHCA	Homo sapiens (human)	0	1
Q9NSP4	Centromere protein M	CENPM C22orf18 ICEN39 PANE1	Homo sapiens (human)	2	1
Q96A26	Protein FAM162A	FAM162A C3orf28 E2IG5	Homo sapiens (human)	0	1
O95198	Kelch-like protein 2	KLHL2	Homo sapiens (human)	0	1
P32969	Large ribosomal subunit protein uL6	RPL9 RPL9P7 RPL9P8 RPL9P9	Homo sapiens (human)	1	1
P50479	PDZ and LIM domain protein 4	PDLIM4 RIL	Homo sapiens (human)	0	1
P40200	T-cell surface protein tactile	CD96	Homo sapiens (human)	15	1
P25789	Proteasome subunit alpha type-4	PSMA4 HC9 PSC9	Homo sapiens (human)	4	1
Q86UQ8	Transcription factor NF-E4	NFE4	Homo sapiens (human)	0	1
O94812	BAI1-associated protein 3	BAIAP3 KIAA0734	Homo sapiens (human)	2	1
P50607	Tubby protein homolog	TUB	Homo sapiens (human)	0	1
A6NKX4	Putative solute carrier family 22 member 31	SLC22A31	Homo sapiens (human)	1	1
O15014	Zinc finger protein 609	ZNF609 KIAA0295	Homo sapiens (human)	7	1
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
Q4W5G0	Tigger transposable element-derived protein 2	TIGD2	Homo sapiens (human)	0	1
Q9C002	Normal mucosa of esophagus-specific gene 1 protein	NMES1 C15orf48	Homo sapiens (human)	4	1
Q8WU39	Marginal zone B- and B1-cell-specific protein	MZB1 MEDA7 PACAP	Homo sapiens (human)	1	1
P33993	DNA replication licensing factor MCM7	MCM7 CDC47 MCM2	Homo sapiens (human)	3	1
Q9H467	CUE domain-containing protein 2	CUEDC2 C10orf66	Homo sapiens (human)	3	1
P21281	V-type proton ATPase subunit B, brain isoform	ATP6V1B2 ATP6B2 VPP3	Homo sapiens (human)	0	1

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