Entry Detail


General Information

Database ID:TRD02363
Confidence:Median
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics
>> Evidence Support
>> Reference



tsRNA Information

tsRNA Name:AS-tDR-006217
tsRNA Type:tRF-3
Amino acid and Anticodon:LysCTT
Sequence:CCCCACGTTGGGCGCCA
Related Target:N/A
Predicted Target:PRX//CHKA//LARP7//OR52N5//PTTG1IP//ST18//SKI//RRAD//SLC1A5//TAF9
External Links:
MINTbase ID:tRF-17-K6MY6V2
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Lys-CTT-4-1
Anticodon:LysCTT
tRNA_number:trna10
Chromosome:16
Strand:+
Coordinate:Start Site(bp): 3241560        End Site(bp): 3241573+3

[2] gtRNAdb_ID:tRNA-Lys-CTT-3-1
Anticodon:LysCTT
tRNA_number:trna32
Chromosome:16
Strand:-
Coordinate:Start Site(bp): 3207406-3        End Site(bp): 3207419

[3] gtRNAdb_ID:tRNA-Lys-CTT-2-1
Anticodon:LysCTT
tRNA_number:trna119
Chromosome:1
Strand:-
Coordinate:Start Site(bp): 145395522-3        End Site(bp): 145395535

[4] gtRNAdb_ID:tRNA-Lys-CTT-2-5
Anticodon:LysCTT
tRNA_number:trna7
Chromosome:16
Strand:+
Coordinate:Start Site(bp): 3225751        End Site(bp): 3225764+3

[5] gtRNAdb_ID:tRNA-Lys-CTT-2-3
Anticodon:LysCTT
tRNA_number:trna11
Chromosome:5
Strand:-
Coordinate:Start Site(bp): 180648979-3        End Site(bp): 180648992

[6] gtRNAdb_ID:tRNA-Lys-CTT-2-2
Anticodon:LysCTT
tRNA_number:trna9
Chromosome:5
Strand:+
Coordinate:Start Site(bp): 180634814        End Site(bp): 180634827+3

[7] gtRNAdb_ID:tRNA-Lys-CTT-2-4
Anticodon:LysCTT
tRNA_number:trna13
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 26556833        End Site(bp): 26556846+3

[8] gtRNAdb_ID:tRNA-Lys-CTT-1-1
Anticodon:LysCTT
tRNA_number:trna13
Chromosome:14
Strand:-
Coordinate:Start Site(bp): 58706613-3        End Site(bp): 58706626

[9] gtRNAdb_ID:tRNA-Lys-CTT-1-2
Anticodon:LysCTT
tRNA_number:trna2
Chromosome:15
Strand:+
Coordinate:Start Site(bp): 79152963        End Site(bp): 79152976+3



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