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 **15401 - 15425** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
O60231	Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16	DHX16 DBP2 DDX16 KIAA0577 PRP2	Homo sapiens (human)	1
Q9NPI1	Bromodomain-containing protein 7	BRD7 BP75 CELTIX1	Homo sapiens (human)	1
Q9UJ70	N-acetyl-D-glucosamine kinase	NAGK	Homo sapiens (human)	1	prostate cancer prostate carcinoma
P41161	ETS translocation variant 5	ETV5 ERM	Homo sapiens (human)	1
Q8WVM0	Dimethyladenosine transferase 1, mitochondrial	TFB1M	Homo sapiens (human)	1
O75955	Flotillin-1	FLOT1	Homo sapiens (human)	1
Q9UNW9	RNA-binding protein Nova-2	NOVA2 ANOVA NOVA3	Homo sapiens (human)	1
Q14240	Eukaryotic initiation factor 4A-II	EIF4A2 DDX2B EIF4F	Homo sapiens (human)	1
O75586	Mediator of RNA polymerase II transcription subunit 6	MED6 ARC33	Homo sapiens (human)	1
Q01650	Large neutral amino acids transporter small subunit 1	SLC7A5 CD98LC LAT1 MPE16	Homo sapiens (human)	1
P10827	Thyroid hormone receptor alpha	THRA EAR7 ERBA1 NR1A1 THRA1 THRA2	Homo sapiens (human)	1
Q5U5X0	Complex III assembly factor LYRM7	LYRM7 C5orf31 MZM1L	Homo sapiens (human)	1
Q13614	Myotubularin-related protein 2	MTMR2 KIAA1073	Homo sapiens (human)	1	Bell's palsy Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease agenesis of the corpus callosum with peripheral neuropathy agnosia axonal neuropathy cancer centronuclear myopathy X-linked centronuclear myopathy clubfoot congenital structural myopathy demyelinating polyneuropathy developmental coordination disorder facial nerve disease facial paralysis familial periodic paralysis glaucoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 motor peripheral neuropathy myopathy neurodegenerative disease neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease polyneuropathy scoliosis sensory peripheral neuropathy stomach cancer stomach carcinoma
O94903	Pyridoxal phosphate homeostasis protein	PLPBP PROSC	Homo sapiens (human)	1
Q9NVX2	Notchless protein homolog 1	NLE1	Homo sapiens (human)	1
Q6ZMW2	Zinc finger protein 782	ZNF782	Homo sapiens (human)	1
A6NKD9	Coiled-coil domain-containing protein 85C	CCDC85C	Homo sapiens (human)	1
O15121	Sphingolipid delta(4)-desaturase DES1	DEGS1 DES1 MLD	Homo sapiens (human)	1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Graves' disease Krabbe disease Pick's disease Reye syndrome acute intermittent porphyria acute interstitial pneumonia acute myocardial infarction alternating hemiplegia of childhood amyloidosis autonomic neuropathy autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 cancer cardiovascular system disease central nervous system disease cerebral degeneration chronic fatigue syndrome colorectal cancer colorectal carcinoma congenital nystagmus coronary thrombosis critical illness polyneuropathy depressive disorder diabetes mellitus diabetic ketoacidosis disease of mental health dissociated nystagmus dysthymic disorder dystonia embryoma encephalitis encephalomyelitis epilepsy esophageal cancer esophageal carcinoma esophagitis essential hypertension gastroesophageal reflux disease giant cell glioblastoma glioblastoma heart disease high grade glioma hyperglycemia hypertension hyperthyroidism idiopathic interstitial pneumonia inflammatory and toxic neuropathy kidney failure large intestine cancer leukodystrophy locked-in syndrome major depressive disorder melancholic depression meningoencephalitis metachromatic leukodystrophy myelitis myocardial infarction nervous system disease neuropathy neurotic disorder obsolete melancholia osteopetrosis osteosclerosis pathologic nystagmus peptic esophagitis peripheral nervous system disease pneumonia polyneuropathy prostate cancer prostate carcinoma psychotic disorder quadriplegia scoliosis silent myocardial infarction spontaneous ocular nystagmus substance abuse substance-related disorder thyrotoxicosis type 2 diabetes mellitus uremia visual epilepsy
Q9BQ61	Telomerase RNA component interacting RNase	TRIR C19orf43	Homo sapiens (human)	1
P10746	Uroporphyrinogen-III synthase	UROS	Homo sapiens (human)	1
Q9BRU9	rRNA-processing protein UTP23 homolog	UTP23 C8orf53	Homo sapiens (human)	1
Q15560	Transcription elongation factor A protein 2	TCEA2	Homo sapiens (human)	1
Q9UL46	Proteasome activator complex subunit 2	PSME2	Homo sapiens (human)	1
Q9Y2K7	Lysine-specific demethylase 2A	KDM2A CXXC8 FBL11 FBL7 FBXL11 JHDM1A KIAA1004	Homo sapiens (human)	1
Q9BX69	Caspase recruitment domain-containing protein 6	CARD6	Homo sapiens (human)	1

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