Entry Detail


General Information

Database ID:TRD01438
Confidence:Median
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics
>> Evidence Support
>> Reference



tsRNA Information

tsRNA Name:AS-tDR-007229
tsRNA Type:i-tRF
Amino acid and Anticodon:TrpCCA
Sequence:ACTCCAGATCAGAAGGCTGCGTG
Related Target:Aak1; Pgm3; Zfp935; Pcmtd2; Pgf; Krt5; Boc; 6720489N17Rik; Gcnt2; Zfp930; AW209491; Mynn; En1; Fam168a; Tbx4; Zfp960; Zfp97; Slc9c1; Satb1; Fryl; Ntm; Ikbip; Eml6; Zfp951; Ptprb; Psme3; Elmod1; Acvr2b; Map4k2; Fshr; Egln1; Ubn1; Hs3st1; Trmt2b; Phka1
Predicted Target:HPS4//ABCA13//UGT1A6//ALK//SEPHS1//PNPLA7//TMEM132C//ARHGEF10//AC019257.8//LUZP2
External Links:
MINTbase ID:tRF-23-ERFMF0QV00
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Trp-CCA-4-1
Anticodon:TrpCCA
tRNA_number:trna6
Chromosome:12
Strand:+
Coordinate:Start Site(bp): 98898059        End Site(bp): 98898081



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:Down-Regulation
Validated Method:High-throughput sequencing
Description:N/A
Comparision:Adriamycin-treated Group VS None
Mechanism:N/A