Entry Detail


General Information

Database ID:TRD00440
Confidence:Median
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics
>> Evidence Support
>> Reference



tsRNA Information

tsRNA Name:AS-tDR-001688
tsRNA Type:i-tRF
Amino acid and Anticodon:ArgTCT
Sequence:TGGATAGCGCATTGGAC
Related Target:N/A
Predicted Target:HES7//FMNL1//KMT2A//ZNF536//KCTD1//SLC35A2//CCDC127//SNX13//OR4L1//AHDC1
External Links:
MINTbase ID:tRF-17-9EFVI81
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Arg-TCT-2-1
Anticodon:ArgTCT
tRNA_number:trna4
Chromosome:17
Strand:+
Coordinate:Start Site(bp): 8024258        End Site(bp): 8024274

[2] gtRNAdb_ID:tRNA-Arg-TCT-5-1
Anticodon:ArgTCT
tRNA_number:trna52
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 27529978        End Site(bp): 27529994

[3] gtRNAdb_ID:tRNA-Arg-TCT-3-2
Anticodon:ArgTCT
tRNA_number:trna3
Chromosome:11
Strand:+
Coordinate:Start Site(bp): 59318782        End Site(bp): 59318798

[4] gtRNAdb_ID:tRNA-Arg-TCT-1-1
Anticodon:ArgTCT
tRNA_number:trna9
Chromosome:1
Strand:+
Coordinate:Start Site(bp): 94313144        End Site(bp): 94313160

[5] gtRNAdb_ID:tRNA-Arg-TCT-3-1
Anticodon:ArgTCT
tRNA_number:trna4
Chromosome:9
Strand:-
Coordinate:Start Site(bp): 131102414        End Site(bp): 131102430



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