Entry Detail


General Information

Database ID:TRD06072
Confidence:Prediction
Confidence Score:0.02 (L1-norm-Graph) & 0.01 (WBNPMD)
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics



tsRNA Information

tsRNA Name:tiRNA-Val-CAC-003
tsRNA Type:5'-tiRNA
Amino acid and Anticodon:ValCAC
Sequence:GTTTCCGTAGTGTAGTGGTTATCACGTTCGCCTC
Related Target:N/A
Predicted Target:ZBED2//CTNND2//SLC12A5//CDYL2//KIAA1549//STK36//CELA2A//ACAP1//CDC25C//HK2
External Links:
MINTbase ID:tRF-34-79MP9P9NH57S15
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Val-CAC-5-1
Anticodon:ValCAC
tRNA_number:trna90
Chromosome:1
Strand:-
Coordinate:Start Site(bp): 149684128        End Site(bp): 149684161

[2] gtRNAdb_ID:tRNA-Val-CAC-4-1
Anticodon:ValCAC
tRNA_number:trna98
Chromosome:1
Strand:-
Coordinate:Start Site(bp): 149298594        End Site(bp): 149298627

[3] gtRNAdb_ID:tRNA-Val-CAC-1-1
Anticodon:ValCAC
tRNA_number:trna85
Chromosome:1
Strand:-
Coordinate:Start Site(bp): 161369529        End Site(bp): 161369562

[4] gtRNAdb_ID:tRNA-Val-CAC-1-5
Anticodon:ValCAC
tRNA_number:trna10
Chromosome:5
Strand:-
Coordinate:Start Site(bp): 180649434        End Site(bp): 180649467

[5] gtRNAdb_ID:tRNA-Val-CAC-1-3
Anticodon:ValCAC
tRNA_number:trna18
Chromosome:5
Strand:-
Coordinate:Start Site(bp): 180529292        End Site(bp): 180529325

[6] gtRNAdb_ID:tRNA-Val-CAC-1-2
Anticodon:ValCAC
tRNA_number:trna2
Chromosome:5
Strand:+
Coordinate:Start Site(bp): 180524070        End Site(bp): 180524103

[7] gtRNAdb_ID:tRNA-Val-CAC-1-4
Anticodon:ValCAC
tRNA_number:trna6
Chromosome:5
Strand:+
Coordinate:Start Site(bp): 180600650        End Site(bp): 180600683

[8] gtRNAdb_ID:tRNA-Val-CAC-1-6
Anticodon:ValCAC
tRNA_number:trna9
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 26538282        End Site(bp): 26538315



tsRNA Association Statistics

Total Associated Disease Number:46
More Information
Network:
(Display the first 15 nodes)



Disease Information

 MeSHDisease Ontology
Disease ID:D028361N/A
Disease Name:Mitochondrial DiseasesN/A
Category:MeSHDisease Ontology
Type:Nutritional and Metabolic DiseasesN/A
Define:Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.N/A
Alias:Electron Transport Chain Deficiencies, Mitochondrial//Mitochondrial Disorders//Mitochondrial Electron Transport Chain Deficiencies//Mitochondrial Respiratory Chain Deficiencies//Oxidative Phosphorylation Deficiencies//Respiratory Chain Deficiencies, MitochondrialN/A



Disease Association Statistics

Total Associated tsRNA Number:69
More Information
Network:
(Display the first 15 nodes)