tsRNADisease

Entry Detail

General Information

Database ID:	TRD02774
Confidence:	Median
Contents:	>> tsRNA Information >> tsRNA Association Statistics >> Disease Information >> Disease Association Statistics >> Evidence Support >> Reference

tsRNA Information

tsRNA Name:

AS-tDR-006555

tsRNA Type:

tRF-3

Amino acid and Anticodon:

ValTAC

Sequence:

GCCCCAGTGGAACCACCA

Related Target:

Mdga2; Slc2a9; Clec10a; Foxj1; Elavl3; Gstt1; Slc8a1; Neurl1a; Sash3; Ppp3r1; Ptov1; Ubp1; Sirt1; 6720489N17Rik; Nufip2; Ranbp9

Predicted Target:

KIAA1522//MDC1//GIMAP4//MARCH1//GIGYF2//SV2C//PLCE1//LIN7B//CNOT6//RASAL3

External Links:

MINTbase ID:	tRF-18-PR18B6D2
tRFdb ID:	N/A

[1] gtRNAdb_ID:	tRNA-Val-TAC-3-1
Anticodon:	ValTAC
tRNA_number:	trna6
Chromosome:	10
Strand:	-
Coordinate:	Start Site(bp): 5895674-3 End Site(bp): 5895688

[2] gtRNAdb_ID:	tRNA-Val-TAC-2-1
Anticodon:	ValTAC
tRNA_number:	trna16
Chromosome:	11
Strand:	-
Coordinate:	Start Site(bp): 59318460-3 End Site(bp): 59318474

[3] gtRNAdb_ID:	tRNA-Val-TAC-1-1
Anticodon:	ValTAC
tRNA_number:	trna17
Chromosome:	11
Strand:	-
Coordinate:	Start Site(bp): 59318102-3 End Site(bp): 59318116

[4] gtRNAdb_ID:	tRNA-Val-TAC-1-2
Anticodon:	ValTAC
tRNA_number:	trna4
Chromosome:	X
Strand:	-
Coordinate:	Start Site(bp): 18693029-3 End Site(bp): 18693043

tsRNA Association Statistics

Total Associated Disease Number:	1 More Information
Network: (Display the first 15 nodes)

Disease Information

	MeSH	Disease Ontology
Disease ID:	D009404	N/A
Disease Name:	Nephrotic Syndrome	N/A
Category:	MeSH	Disease Ontology
Type:	N/A	N/A
Define:	N/A	N/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//Nphs3	N/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