Entry Detail


General Information

Database ID:TRD02727
Confidence:Median
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics
>> Evidence Support
>> Reference



tsRNA Information

tsRNA Name:tRF-Tyr-GTA-005
tsRNA Type:tRF-3
Amino acid and Anticodon:TyrGTA
Sequence:TCCGGCTCGAAGGACCA
Related Target:N/A
Predicted Target:KLHDC4//GAD2//CHST3//CHD2//TMEM41A//IPO13//CCDC106//DUS2//NRROS//STMN3
External Links:
MINTbase ID:tRF-17-884U1D2
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Tyr-GTA-5-3
Anticodon:TyrGTA
tRNA_number:trna19
Chromosome:14
Strand:-
Coordinate:Start Site(bp): 21121258-3        End Site(bp): 21121271

[2] gtRNAdb_ID:tRNA-Tyr-GTA-7-1
Anticodon:TyrGTA
tRNA_number:trna17
Chromosome:14
Strand:-
Coordinate:Start Site(bp): 21128117-3        End Site(bp): 21128130

[3] gtRNAdb_ID:tRNA-Tyr-GTA-5-4
Anticodon:TyrGTA
tRNA_number:trna16
Chromosome:14
Strand:-
Coordinate:Start Site(bp): 21131351-3        End Site(bp): 21131364

[4] gtRNAdb_ID:tRNA-Tyr-GTA-5-5
Anticodon:TyrGTA
tRNA_number:trna5
Chromosome:14
Strand:+
Coordinate:Start Site(bp): 21151507        End Site(bp): 21151520+3

[5] gtRNAdb_ID:tRNA-Tyr-GTA-1-1
Anticodon:TyrGTA
tRNA_number:trna14
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 26569163        End Site(bp): 26569176+3

[6] gtRNAdb_ID:tRNA-Tyr-GTA-8-1
Anticodon:TyrGTA
tRNA_number:trna15
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 26575874        End Site(bp): 26575887+3

[7] gtRNAdb_ID:tRNA-Tyr-GTA-2-1
Anticodon:TyrGTA
tRNA_number:trna2
Chromosome:2
Strand:+
Coordinate:Start Site(bp): 27273725        End Site(bp): 27273738+3

[8] gtRNAdb_ID:tRNA-Tyr-GTA-5-1
Anticodon:TyrGTA
tRNA_number:trna4
Chromosome:8
Strand:+
Coordinate:Start Site(bp): 67025681        End Site(bp): 67025694+3

[9] gtRNAdb_ID:tRNA-Tyr-GTA-5-2
Anticodon:TyrGTA
tRNA_number:trna5
Chromosome:8
Strand:+
Coordinate:Start Site(bp): 67026298        End Site(bp): 67026311+3



tsRNA Association Statistics

Total Associated Disease Number:22
More Information
Network:
(Display the first 15 nodes)



Disease Information

 MeSHDisease Ontology
Disease ID:D006333N/A
Disease Name:Heart FailureN/A
Category:MeSHDisease Ontology
Type:Cardiovascular DiseasesN/A
Define:A heterogeneous condition in which the heart is unable to pump out sufficient blood to meet the metabolic need of the body. Heart failure can be caused by structural defects, functional abnormalities (VENTRICULAR DYSFUNCTION), or a sudden overload beyond its capacity. Chronic heart failure is more common than acute heart failure which results from sudden insult to cardiac function, such as MYOCARDIAL INFARCTION.N/A
Alias:Cardiac Failure//Congestive Heart Failure//Heart Decompensation//Heart Failure, Congestive//Heart Failure, Left-Sided//Heart Failure, Right-Sided//Left-Sided Heart Failure//Myocardial Failure//Right-Sided Heart FailureN/A



Disease Association Statistics

Total Associated tsRNA Number:81
More Information
Network:
(Display the first 15 nodes)



Evidence Support

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



Reference

[1] PubMed ID:37839439
Disease Name:Heart Failure
Tissue:Epicardial Adipose Tissue
Dysfunction Pattern:Down-Regulation
Validated Method:High-throughput sequencing//Data Mining
Description:Of those, a total of 24 tsRNAs were significantly differentially expressed between HF and controls: 17 were upregulated and 7 were downregulated (fold change >1.5, p < 0.05).
Comparision:HF VS Control
Mechanism:N/A