Entry Detail


General Information

Database ID:TRD00597
Confidence:Median
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics
>> Evidence Support
>> Reference



tsRNA Information

tsRNA Name:AS-tDR-001980
tsRNA Type:i-tRF
Amino acid and Anticodon:CysGCA;CysACA
Sequence:TGGTAGAGCATTTGACT
Related Target:N/A
Predicted Target:IBTK//YIPF6//CARS2//TKFC//GABRG2//TRIM26//KIAA0319//RHOB//SORCS2//AGO1
External Links:
MINTbase ID:tRF-17-9L5FZU3
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Cys-GCA-7-1
Anticodon:CysGCA
tRNA_number:trna127
Chromosome:1
Strand:-
Coordinate:Start Site(bp): 93981874        End Site(bp): 93981890

[2] gtRNAdb_ID:tRNA-Cys-GCA-6-1
Anticodon:CysGCA
tRNA_number:trna7
Chromosome:3
Strand:-
Coordinate:Start Site(bp): 131947984        End Site(bp): 131948000

[3] gtRNAdb_ID:tRNA-Cys-GCA-4-1
Anticodon:CysGCA
tRNA_number:trna28
Chromosome:17
Strand:-
Coordinate:Start Site(bp): 37025585        End Site(bp): 37025601

[4] gtRNAdb_ID:tRNA-Cys-GCA-2-2
Anticodon:CysGCA
tRNA_number:trna15
Chromosome:17
Strand:+
Coordinate:Start Site(bp): 37023913        End Site(bp): 37023929

[5] gtRNAdb_ID:tRNA-Cys-GCA-2-4
Anticodon:CysGCA
tRNA_number:trna26
Chromosome:17
Strand:-
Coordinate:Start Site(bp): 37310784        End Site(bp): 37310800

[6] gtRNAdb_ID:tRNA-Cys-GCA-2-3
Anticodon:CysGCA
tRNA_number:trna27
Chromosome:17
Strand:-
Coordinate:Start Site(bp): 37310027        End Site(bp): 37310043

[7] gtRNAdb_ID:tRNA-Cys-GCA-2-1
Anticodon:CysGCA
tRNA_number:trna3
Chromosome:4
Strand:-
Coordinate:Start Site(bp): 124430045        End Site(bp): 124430061

[8] gtRNAdb_ID:tRNA-Cys-GCA-1-1
Anticodon:CysGCA
tRNA_number:trna5
Chromosome:7
Strand:+
Coordinate:Start Site(bp): 149007296        End Site(bp): 149007312

[9] gtRNAdb_ID:tRNA-Cys-ACA-1-1
Anticodon:CysACA
tRNA_number:trna1
Chromosome:5
Strand:+
Coordinate:Start Site(bp): 151988611        End Site(bp): 151988627



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