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 **17876 - 17900** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
O14829	Serine/threonine-protein phosphatase with EF-hands 1	PPEF1 PPEF PPP7C	Homo sapiens (human)	1
Q86YE8	Zinc finger protein 573	ZNF573	Homo sapiens (human)	1
Q8N9A8	Nuclear envelope phosphatase-regulatory subunit 1	CNEP1R1 C16orf69 TMEM188	Homo sapiens (human)	1
A8MZ59	Paired-like homeodomain transcription factor LEUTX	LEUTX	Homo sapiens (human)	1
Q01130	Serine/arginine-rich splicing factor 2	SRSF2 SFRS2	Homo sapiens (human)	1
Q9H0U6	Large ribosomal subunit protein uL18m	MRPL18	Homo sapiens (human)	1
P25208	Nuclear transcription factor Y subunit beta	NFYB HAP3	Homo sapiens (human)	1
Q8IZU0	Protein FAM9B	FAM9B	Homo sapiens (human)	1
O75569	Interferon-inducible double-stranded RNA-dependent protein kinase activator A	PRKRA PACT RAX	Homo sapiens (human)	1
Q8N6M0	Deubiquitinase OTUD6B	OTUD6B DUBA5	Homo sapiens (human)	1
Q96BH1	E3 ubiquitin-protein ligase RNF25	RNF25	Homo sapiens (human)	1
Q5I7T1	Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase	ALG10B KCR1	Homo sapiens (human)	1	long QT syndrome 2 long QT syndrome sick sinus syndrome
Q8N4P2	Intraflagellar transport protein 70B	IFT70B TTC30B	Homo sapiens (human)	1
P09496	Clathrin light chain A	CLTA	Homo sapiens (human)	1
P55347	Homeobox protein PKNOX1	PKNOX1 PREP1	Homo sapiens (human)	1
Q9HCH0	Nck-associated protein 5-like	NCKAP5L CEP169 KIAA1602	Homo sapiens (human)	1
Q9BRJ7	Tudor-interacting repair regulator protein	NUDT16L1 SDOS TIRR	Homo sapiens (human)	1
Q9UJ41	Rab5 GDP/GTP exchange factor	RABGEF1 RABEX5	Homo sapiens (human)	1
Q8IZ73	Pseudouridylate synthase RPUSD2	RPUSD2 C15orf19	Homo sapiens (human)	1
Q0VFZ6	Cilia- and flagella- associated protein 210	CFAP210 C2orf77 CCDC173	Homo sapiens (human)	1
Q9NZ32	Actin-related protein 10	ACTR10 ACTR11 ARP10 ARP11	Homo sapiens (human)	1
P69892	Hemoglobin subunit gamma-2	HBG2	Homo sapiens (human)	1
O95361	Tripartite motif-containing protein 16	TRIM16 EBBP	Homo sapiens (human)	1
Q4J6C6	Prolyl endopeptidase-like	PREPL KIAA0436	Homo sapiens (human)	1
Q04446	1,4-alpha-glucan-branching enzyme	GBE1	Homo sapiens (human)	1	B-cell lymphoma Cauda equina syndrome Fabry disease Gerstmann-Straussler-Scheinker syndrome Gorham's disease Guillain-Barre syndrome Noonan syndrome 1 acute myeloid leukemia bronchus cancer bronchus carcinoma cancer cardiomyopathy carnitine palmitoyltransferase II deficiency cerebral infarction cerebrovascular disease chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy chronic ulcer of skin chylomicron retention disease congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congestive heart failure contractures, pterygia, and spondylocarpotarsal fusion syndrome cystinuria cytochrome-c oxidase deficiency disease dementia diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism embryoma endomyocardial fibrosis esophagus squamous cell carcinoma familial lipoprotein lipase deficiency familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease VI glycogen storage disease VII glycogen storage disease hypertrophic cardiomyopathy idiopathic scoliosis intellectual disability learning disability leukodystrophy lipid storage disease liver disease locked-in syndrome lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma megaconial type congenital muscular dystrophy melanoma mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myopathy nemaline myopathy neurogenic bladder obsolete ymphosarcoma ovarian cancer ovarian carcinoma paraplegia polyhydramnios porphyria portal hypertension quadriplegia rigid spine muscular dystrophy 1 skin melanoma

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