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 **1101 - 1125** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q9JMH6	Thioredoxin reductase 1, cytoplasmic	Txnrd1 Trxr1	Mus musculus (house mouse)	1
V5BT91	Prostaglandin F2alpha synthase	TCDM_00059	Trypanosoma cruzi Dm28c	1
Q3TH57	Transcription elongation regulator 1	Tcerg1	Mus musculus (house mouse)	1
V5B7R2	cytochrome-b5 reductase	TCDM_08466	Trypanosoma cruzi Dm28c	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
Q5EG47	5'-AMP-activated protein kinase catalytic subunit alpha-1	Prkaa1	Mus musculus (house mouse)	1
Q9DBH0	NEDD4-like E3 ubiquitin-protein ligase WWP2	Wwp2	Mus musculus (house mouse)	1
A0A286YD12	Neurolysin, mitochondrial	Nln	Mus musculus (house mouse)	1
Q9NVX2	Notchless protein homolog 1	NLE1	Homo sapiens (human)	1
Q6ZMW2	Zinc finger protein 782	ZNF782	Homo sapiens (human)	1
K2NFF1	Uncharacterized protein	MOQ_002515	Trypanosoma cruzi marinkellei	1
A6NKD9	Coiled-coil domain-containing protein 85C	CCDC85C	Homo sapiens (human)	1
Q4E0G0	C2 domain-containing protein	Tc00.1047053510155.140	Trypanosoma cruzi strain CL Brener	1
Q4DU38	Calcium motive p-type ATPase, putative	Tc00.1047053506241.70	Trypanosoma cruzi strain CL Brener	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
Q6ZPE2	Myotubularin-related protein 5	Sbf1 Kiaa3020 Mtmr5	Mus musculus (house mouse)	1
Q9BQ61	Telomerase RNA component interacting RNase	TRIR C19orf43	Homo sapiens (human)	1
E9QKI2	Potassium voltage gated channel, Shaw-related subfamily, member 3	Kcnc3	Mus musculus (house mouse)	1
P10746	Uroporphyrinogen-III synthase	UROS	Homo sapiens (human)	1
V5B7L4	DNA-directed RNA polymerase subunit beta	TCDM_01995	Trypanosoma cruzi Dm28c	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
E9Q9H2	DnaJ homolog subfamily C member 2	Dnajc2	Mus musculus (house mouse)	1
Q9UL46	Proteasome activator complex subunit 2	PSME2	Homo sapiens (human)	1

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