Entry Detail


General Information

Database ID:TRD05975
Confidence:Prediction
Confidence Score:0.00 (L1-norm-Graph) & 0.00 (WBNPMD)
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics



tsRNA Information

tsRNA Name:tiRNA-Val-AAC-002
tsRNA Type:5'-tiRNA
Amino acid and Anticodon:ValAAC
Sequence:GTTTCCGTAGTGTAGTGGTTATCACGTTCGCCTA
Related Target:N/A
Predicted Target:ZBED2//CTNND2//CDYL2//SLC12A5//KIAA1549//HK2//CLSTN3//CELA2A//ACAP1//LRRN3
External Links:
MINTbase ID:tRF-34-79MP9P9NH57S1O
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Val-AAC-4-1
Anticodon:ValAAC
tRNA_number:trna136
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 27648924        End Site(bp): 27648957

[2] gtRNAdb_ID:tRNA-Val-AAC-3-1
Anticodon:ValAAC
tRNA_number:trna139
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 27618746        End Site(bp): 27618779

[3] gtRNAdb_ID:tRNA-Val-AAC-1-1
Anticodon:ValAAC
tRNA_number:trna2
Chromosome:3
Strand:+
Coordinate:Start Site(bp): 169490018        End Site(bp): 169490051

[4] gtRNAdb_ID:tRNA-Val-AAC-1-4
Anticodon:ValAAC
tRNA_number:trna12
Chromosome:5
Strand:-
Coordinate:Start Site(bp): 180645309        End Site(bp): 180645342

[5] gtRNAdb_ID:tRNA-Val-AAC-1-2
Anticodon:ValAAC
tRNA_number:trna4
Chromosome:5
Strand:+
Coordinate:Start Site(bp): 180591154        End Site(bp): 180591187

[6] gtRNAdb_ID:tRNA-Val-AAC-1-3
Anticodon:ValAAC
tRNA_number:trna5
Chromosome:5
Strand:+
Coordinate:Start Site(bp): 180596610        End Site(bp): 180596643

[7] gtRNAdb_ID:tRNA-Val-AAC-1-5
Anticodon:ValAAC
tRNA_number:trna132
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 27721218        End Site(bp): 27721251



tsRNA Association Statistics

Total Associated Disease Number:35
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)