Entry Detail



General Information

Database ID:TRD01273
Confidence:Median
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics
>> Evidence Support
>> Reference



tsRNA Information

tsRNA Name:AS-tDR-004493
tsRNA Type:i-tRF
Amino acid and Anticodon:MetCAT
Sequence:CCCATAACCCAGAGGTCGATG
Related Target:N/A
Predicted Target:UTP4//PHKG2//CCDC154//NUFIP2//SPRYD4//TSPAN17//GFAP//MRPL19//RBM43//PCDHGC5
External Links:
MINTbase ID:tRF-21-KQBRFKWE0
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-iMet-CAT-2-1
Anticodon:MetCAT
tRNA_number:trna61
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 27745694        End Site(bp): 27745714

[2] gtRNAdb_ID:tRNA-iMet-CAT-1-1
Anticodon:MetCAT
tRNA_number:trna32
Chromosome:1
Strand:+
Coordinate:Start Site(bp): 153643756        End Site(bp): 153643776

[3] gtRNAdb_ID:tRNA-iMet-CAT-1-8
Anticodon:MetCAT
tRNA_number:trna20
Chromosome:17
Strand:-
Coordinate:Start Site(bp): 80452618        End Site(bp): 80452638

[4] gtRNAdb_ID:tRNA-iMet-CAT-1-7
Anticodon:MetCAT
tRNA_number:trna129
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 27870292        End Site(bp): 27870312

[5] gtRNAdb_ID:tRNA-iMet-CAT-1-6
Anticodon:MetCAT
tRNA_number:trna142
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 27560621        End Site(bp): 27560641

[6] gtRNAdb_ID:tRNA-iMet-CAT-1-5
Anticodon:MetCAT
tRNA_number:trna150
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 27300785        End Site(bp): 27300805

[7] gtRNAdb_ID:tRNA-iMet-CAT-1-4
Anticodon:MetCAT
tRNA_number:trna169
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 26330550        End Site(bp): 26330570

[8] gtRNAdb_ID:tRNA-iMet-CAT-1-3
Anticodon:MetCAT
tRNA_number:trna171
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 26313373        End Site(bp): 26313393

[9] gtRNAdb_ID:tRNA-iMet-CAT-1-2
Anticodon:MetCAT
tRNA_number:trna2
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 26286784        End Site(bp): 26286804



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