Entry Detail


General Information

Database ID:TRD02632
Confidence:Median
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics
>> Evidence Support
>> Reference



tsRNA Information

tsRNA Name:AS-tDR-006242
tsRNA Type:tRF-3
Amino acid and Anticodon:ThrCGT
Sequence:CCCCGTCCGTGCCTCCA
Related Target:N/A
Predicted Target:ZNF282//CXXC4//SLC22A18//OBSL1//SHOC2//NBL1//UBALD1//LSS//SRRM3//OTUD7A
External Links:
MINTbase ID:tRF-17-KS8WP92
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Thr-CGT-4-1
Anticodon:ThrCGT
tRNA_number:trna14
Chromosome:17
Strand:+
Coordinate:Start Site(bp): 29877151        End Site(bp): 29877164+3

[2] gtRNAdb_ID:tRNA-Thr-CGT-2-1
Anticodon:ThrCGT
tRNA_number:trna15
Chromosome:16
Strand:+
Coordinate:Start Site(bp): 14379808        End Site(bp): 14379821+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