Entry Detail



General Information

Database ID:TRD00906
Confidence:Very High
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics
>> Evidence Support
>> Reference



tsRNA Information

tsRNA Name:tRF-47
tsRNA Type:i-tRF
Amino acid and Anticodon:GluTTC
Sequence:GATGGTTTTTCATATCATTGGTCGTGGTTGTAGTCCGTGCGAGAATA
Related Target:N/A
Predicted Target:MYO10//SNX31//ARHGAP42//HDAC6//HNRNPH3//GART//RMND5A//UBR1//CLDN10//ELOF1
External Links:
MINTbase ID:tRF-47-58ZZJQJYSWRYVMMV5BO
tRFdb ID:N/A

[1] gtRNAdb_ID:-
Anticodon:GluTTC
tRNA_number:trnaMT
Chromosome:MT
Strand:-
Coordinate:Start Site(bp): 14674        End Site(bp): 14720

[2] gtRNAdb_ID:-
Anticodon:GluTTC
tRNA_number:trnalookalike8
Chromosome:5
Strand:-
Coordinate:Start Site(bp): 93905172        End Site(bp): 93905218



tsRNA Association Statistics

Total Associated Disease Number:4
More Information
Network:
(Display the first 15 nodes)



Disease Information

 MeSHDisease Ontology
Disease ID:D065626DOID:0080546
Disease Name:Non-alcoholic Fatty Liver Diseasenon-alcoholic fatty liver
Category:MeSHDisease Ontology
Type:Digestive System Diseasesdisease of anatomical entity//disease of metabolism//genetic disease
Define:Fatty liver finding without excessive ALCOHOL CONSUMPTION.A metabolic dysfunction-associated steatotic liver disease characterized by the absence of inflammation and hepatocyte injury in the form of hepatocyte ballooning.
Alias:Fatty Liver, Nonalcoholic//NAFLD//Nonalcoholic Fatty Liver Disease//Nonalcoholic SteatohepatitisNAFL//nonalcoholic fatty liver



Disease Association Statistics

Total Associated tsRNA Number:48
More Information
Network:
(Display the first 15 nodes)



Evidence Support

Strong Evidence:Transfection
Weak Evidence:High-throughput sequencing



Reference

[1] PubMed ID:35287671
Disease Name:Non-alcoholic Fatty Liver Disease
Tissue:Serum Samples
Dysfunction Pattern:Up-Regulation
Validated Method:Transfection//High-throughput sequencing
Description:Then, small RNA sequencing revealed that TEC up-regulated the expression of tRF-47-58ZZJQJYSWRYVMMV5BO (tRF-47). The knockdown of tRF-47 blunted the beneficial effects of TEC on NASH in vitro, including inhibition of autophagy, activation of pyroptosis and release of inflammatory factors.
Comparision:TEC VS Control
Mechanism:These results demonstrated that tRF-47-mediated autophagy and pyroptosis plays a vital role in the function of TEC to treat NASH, suggesting that TEC may be a promising drug for the treatment of NASH.