Entry Detail



General Information

Database ID:TRD02980
Confidence:Median
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics
>> Evidence Support
>> Reference



tsRNA Information

tsRNA Name:tRF-24-R29P4P9LH9
tsRNA Type:tRF-5
Amino acid and Anticodon:AlaTGC
Sequence:GGGGATGTAGCTCAGTGGTAGAGC
Related Target:N/A
Predicted Target:GPR84//ITPR3//ZBTB7B//SGSM2//ABCA3//PAQR5//ADAM11//GPR142//C1orf94//ALDH9A1
External Links:
MINTbase ID:tRF-24-R29P4P9LH9
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Ala-AGC-4-1
Anticodon:AlaAGC
tRNA_number:trna120
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 28626062        End Site(bp): 28626085

[2] gtRNAdb_ID:tRNA-Ala-CGC-3-1
Anticodon:AlaCGC
tRNA_number:trna13
Chromosome:2
Strand:+
Coordinate:Start Site(bp): 157257281        End Site(bp): 157257304

[3] gtRNAdb_ID:tRNA-Ala-CGC-2-1
Anticodon:AlaCGC
tRNA_number:trna119
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 28641661        End Site(bp): 28641684

[4] gtRNAdb_ID:tRNA-Ala-CGC-1-1
Anticodon:AlaCGC
tRNA_number:trna10
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 26553731        End Site(bp): 26553754

[5] gtRNAdb_ID:tRNA-Ala-TGC-4-1
Anticodon:AlaTGC
tRNA_number:trna8
Chromosome:12
Strand:+
Coordinate:Start Site(bp): 125424512        End Site(bp): 125424535

[6] gtRNAdb_ID:tRNA-Ala-TGC-3-2
Anticodon:AlaTGC
tRNA_number:trna13
Chromosome:12
Strand:-
Coordinate:Start Site(bp): 125406349        End Site(bp): 125406372

[7] gtRNAdb_ID:tRNA-Ala-TGC-3-1
Anticodon:AlaTGC
tRNA_number:trna8
Chromosome:5
Strand:+
Coordinate:Start Site(bp): 180633868        End Site(bp): 180633891

[8] gtRNAdb_ID:tRNA-Ala-TGC-2-1
Anticodon:AlaTGC
tRNA_number:trna66
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 28611222        End Site(bp): 28611245



tsRNA Association Statistics

Total Associated Disease Number:2
More Information
Network:
(Display the first 15 nodes)



Disease Information

 MeSHDisease Ontology
Disease ID:D004827DOID:1826
Disease Name:Epilepsyepilepsy
Category:MeSHDisease Ontology
Type:Nervous System Diseasesdisease of anatomical entity
Define:A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313)A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.
Alias:Aura//Awakening Epilepsy//Epilepsy, Cryptogenic//Seizure Disorderepilepsy syndrome//epileptic syndrome



Disease Association Statistics

Total Associated tsRNA Number:47
More Information
Network:
(Display the first 15 nodes)



Evidence Support

Strong Evidence:N/A
Weak Evidence:High-throughput sequencing



Reference

[1] PubMed ID:31039137
Disease Name:Epilepsy
Tissue:Blood
Dysfunction Pattern:Up-Regulation
Validated Method:High-throughput sequencing
Description:N/A
Comparision:Disease VS Control
Mechanism:N/A