Entry Detail


General Information

Database ID:TRD00652
Confidence:Median
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics
>> Evidence Support
>> Reference



tsRNA Information

tsRNA Name:AS-tDR-002232
tsRNA Type:i-tRF
Amino acid and Anticodon:GlnTTG
Sequence:ACTCTGGACTTTGAATC
Related Target:N/A
Predicted Target:ZNF518A//MYOM3//SBDS//SP110//ADAMTS5//C4orf50//EYA4//CREG1//RAD54L//ELP1
External Links:
MINTbase ID:tRF-17-E76IZB5
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Gln-TTG-3-3
Anticodon:GlnTTG
tRNA_number:trna130
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 27763672        End Site(bp): 27763688

[2] gtRNAdb_ID:tRNA-Gln-TTG-3-2
Anticodon:GlnTTG
tRNA_number:trna173
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 26312007        End Site(bp): 26312023

[3] gtRNAdb_ID:tRNA-Gln-TTG-3-1
Anticodon:GlnTTG
tRNA_number:trna174
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 26311456        End Site(bp): 26311472

[4] gtRNAdb_ID:tRNA-Gln-TTG-2-1
Anticodon:GlnTTG
tRNA_number:trna64
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 28557179        End Site(bp): 28557195

[5] gtRNAdb_ID:tRNA-Gln-TTG-1-1
Anticodon:GlnTTG
tRNA_number:trna16
Chromosome:17
Strand:+
Coordinate:Start Site(bp): 47269913        End Site(bp): 47269929



tsRNA Association Statistics

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



Disease Information

 MeSHDisease Ontology
Disease ID:D009404N/A
Disease Name:Nephrotic SyndromeN/A
Category:MeSHDisease Ontology
Type:N/AN/A
Define:N/AN/A
Alias:Congenital nephrotic syndrome 1//Congenital nephrotic syndrome, Finnish type//Finnish congenital nephrosis//Nephrosis 1, congenital, Finnish type//Nephrotic Syndrome, Early-Onset, Type 3//Nephrotic Syndrome, Idiopathic//Nephrotic Syndrome, Type 1//Nephrotic Syndrome, Type 2//Nephrotic Syndrome, Type 3//Nphs3N/A



Disease Association Statistics

Total Associated tsRNA Number:209
More Information
Network:
(Display the first 15 nodes)



Evidence Support

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



Reference

[1] PubMed ID:32685525
Disease Name:Nephrotic Syndrome
Tissue:Podocyte
Dysfunction Pattern:Up-Regulation
Validated Method:High-throughput sequencing
Description:N/A
Comparision:Adriamycin-treated Group VS None
Mechanism:N/A