Entry Detail


General Information

Database ID:TRD02623
Confidence:Median
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics
>> Evidence Support
>> Reference



tsRNA Information

tsRNA Name:AS-tDR-006953
tsRNA Type:tRF-3
Amino acid and Anticodon:ThrAGT
Sequence:TCGAATCCCAGCGGTGCCTCCA
Related Target:N/A
Predicted Target:PRPSAP2//PSMG4//NAA35//CRTAP//SLC43A3//EPB41L5//KCTD11//ZFP69//RASIP1//NR2C2AP
External Links:
MINTbase ID:tRF-22-WB86Q3P92
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Thr-AGT-5-1
Anticodon:ThrAGT
tRNA_number:trna40
Chromosome:17
Strand:-
Coordinate:Start Site(bp): 8042770-3        End Site(bp): 8042788

[2] gtRNAdb_ID:tRNA-Thr-AGT-1-2
Anticodon:ThrAGT
tRNA_number:trna36
Chromosome:17
Strand:-
Coordinate:Start Site(bp): 8129553-3        End Site(bp): 8129571

[3] gtRNAdb_ID:tRNA-Thr-AGT-1-1
Anticodon:ThrAGT
tRNA_number:trna8
Chromosome:17
Strand:+
Coordinate:Start Site(bp): 8090533        End Site(bp): 8090551+3

[4] gtRNAdb_ID:tRNA-Thr-AGT-1-3
Anticodon:ThrAGT
tRNA_number:trna4
Chromosome:19
Strand:+
Coordinate:Start Site(bp): 33668018        End Site(bp): 33668036+3



tsRNA Association Statistics

Total Associated Disease Number:1
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