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 **4026 - 4050** 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
Q5SRI9	Glycoprotein endo-alpha-1,2-mannosidase	MANEA	Homo sapiens (human)	5	1	anxiety disorder autoimmune disease autoimmune lymphoproliferative syndrome breast cancer cancer cocaine abuse cocaine dependence delusional disorder disease of mental health embryoma endocarditis immune system disease infective endocarditis morphine dependence panic disorder paranoid schizophrenia phobic disorder polycystic ovary syndrome psychotic disorder social phobia subacute bacterial endocarditis
Q96HR8	H/ACA ribonucleoprotein complex non-core subunit NAF1	NAF1	Homo sapiens (human)	0	1
P60880	Synaptosomal-associated protein 25	SNAP25 SNAP	Homo sapiens (human)	1	1
O76041	Nebulette	NEBL C10orf113 LNEBL	Homo sapiens (human)	2	1
O60336	Mitogen-activated protein kinase-binding protein 1	MAPKBP1 JNKBP1 KIAA0596	Homo sapiens (human)	0	1
Q9HAB8	Phosphopantothenate--cysteine ligase	PPCS COAB	Homo sapiens (human)	0	1
Q9NZ63	Splicing factor C9orf78	C9orf78 HCA59	Homo sapiens (human)	0	1
Q9Y5L0	Transportin-3	TNPO3 IPO12	Homo sapiens (human)	0	1
Q5TID7	Coiled-coil domain-containing protein 181	CCDC181 C1orf114	Homo sapiens (human)	0	1
A2RU48	Single-pass membrane and coiled-coil domain-containing protein 3	SMCO3 C12orf69	Homo sapiens (human)	1	1
O95816	BAG family molecular chaperone regulator 2	BAG2	Homo sapiens (human)	1	1
P55042	GTP-binding protein RAD	RRAD RAD	Homo sapiens (human)	1	1
P43363	Melanoma-associated antigen 10	MAGEA10 MAGE10	Homo sapiens (human)	0	1
Q9Y261	Hepatocyte nuclear factor 3-beta	FOXA2 HNF3B TCF3B	Homo sapiens (human)	0	1
Q9BV35	Mitochondrial adenyl nucleotide antiporter SLC25A23	SLC25A23 APC2 MCSC2 SCAMC3	Homo sapiens (human)	1	1
Q8WVR3	Trafficking protein particle complex subunit 14	TRAPPC14 C7orf43 MAP11	Homo sapiens (human)	2	1
Q8IY21	Probable ATP-dependent RNA helicase DDX60	DDX60	Homo sapiens (human)	0	1
Q99832	T-complex protein 1 subunit eta	CCT7 CCTH NIP7-1	Homo sapiens (human)	0	1
Q96PV7	Protein FAM193B	FAM193B IRIZIO KIAA1931	Homo sapiens (human)	0	1
Q9BPX5	Actin-related protein 2/3 complex subunit 5-like protein	ARPC5L	Homo sapiens (human)	1	1
Q07955	Serine/arginine-rich splicing factor 1	SRSF1 ASF SF2 SF2P33 SFRS1	Homo sapiens (human)	0	1
Q14896	Myosin-binding protein C, cardiac-type	MYBPC3	Homo sapiens (human)	3	1
Q6GPH4	XIAP-associated factor 1	XAF1 BIRC4BP XIAPAF1	Homo sapiens (human)	0	1
P11310	Medium-chain specific acyl-CoA dehydrogenase, mitochondrial	ACADM	Homo sapiens (human)	1	1	D-bifunctional protein deficiency Reye syndrome brain edema breast cancer breast carcinoma cancer carnitine palmitoyltransferase I deficiency chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma congestive heart failure cystinuria diarrhea disease of metabolism distal arthrogryposis epilepsy familial periodic paralysis galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatitis hydrocephalus hypoglycemia hypoglycemic coma inherited metabolic disorder isolated elevated serum creatine phosphokinase levels lactic acidosis large intestine cancer liver disease long QT syndrome medium chain acyl-CoA dehydrogenase deficiency metabolic dysfunction-associated steatotic liver disease myopathy neuroblastoma neurodegenerative disease nonpapillary renal cell carcinoma obesity papillary renal cell carcinoma perinatal necrotizing enterocolitis phenylketonuria pseudosarcomatous fibromatosis psoriatic arthritis renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma sick sinus syndrome steatotic liver disease sudden infant death syndrome systemic primary carnitine deficiency disease urea cycle disorder visual epilepsy
Q9UJQ4	Sal-like protein 4	SALL4 ZNF797	Homo sapiens (human)	2	1

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