Entry Detail


General Information

Database ID:TRD07685
Confidence:Prediction
Confidence Score:0.01 (L1-norm-Graph) & 0.02 (WBNPMD)
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics



tsRNA Information

tsRNA Name:tRF-Tyr-GTA-005
tsRNA Type:tRF-3
Amino acid and Anticodon:TyrGTA
Sequence:TCCGGCTCGAAGGACCA
Related Target:N/A
Predicted Target:KLHDC4//GAD2//CHST3//CHD2//TMEM41A//IPO13//CCDC106//DUS2//NRROS//STMN3
External Links:
MINTbase ID:tRF-17-884U1D2
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Tyr-GTA-5-3
Anticodon:TyrGTA
tRNA_number:trna19
Chromosome:14
Strand:-
Coordinate:Start Site(bp): 21121258-3        End Site(bp): 21121271

[2] gtRNAdb_ID:tRNA-Tyr-GTA-7-1
Anticodon:TyrGTA
tRNA_number:trna17
Chromosome:14
Strand:-
Coordinate:Start Site(bp): 21128117-3        End Site(bp): 21128130

[3] gtRNAdb_ID:tRNA-Tyr-GTA-5-4
Anticodon:TyrGTA
tRNA_number:trna16
Chromosome:14
Strand:-
Coordinate:Start Site(bp): 21131351-3        End Site(bp): 21131364

[4] gtRNAdb_ID:tRNA-Tyr-GTA-5-5
Anticodon:TyrGTA
tRNA_number:trna5
Chromosome:14
Strand:+
Coordinate:Start Site(bp): 21151507        End Site(bp): 21151520+3

[5] gtRNAdb_ID:tRNA-Tyr-GTA-1-1
Anticodon:TyrGTA
tRNA_number:trna14
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 26569163        End Site(bp): 26569176+3

[6] gtRNAdb_ID:tRNA-Tyr-GTA-8-1
Anticodon:TyrGTA
tRNA_number:trna15
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 26575874        End Site(bp): 26575887+3

[7] gtRNAdb_ID:tRNA-Tyr-GTA-2-1
Anticodon:TyrGTA
tRNA_number:trna2
Chromosome:2
Strand:+
Coordinate:Start Site(bp): 27273725        End Site(bp): 27273738+3

[8] gtRNAdb_ID:tRNA-Tyr-GTA-5-1
Anticodon:TyrGTA
tRNA_number:trna4
Chromosome:8
Strand:+
Coordinate:Start Site(bp): 67025681        End Site(bp): 67025694+3

[9] gtRNAdb_ID:tRNA-Tyr-GTA-5-2
Anticodon:TyrGTA
tRNA_number:trna5
Chromosome:8
Strand:+
Coordinate:Start Site(bp): 67026298        End Site(bp): 67026311+3



tsRNA Association Statistics

Total Associated Disease Number:22
More Information
Network:
(Display the first 15 nodes)



Disease Information

 MeSHDisease Ontology
Disease ID:D001281DOID:0060224
Disease Name:Atrial Fibrillationatrial fibrillation
Category:MeSHDisease Ontology
Type:Cardiovascular Diseases//Pathological Conditions, Signs and Symptomsdisease of anatomical entity
Define:Abnormal cardiac rhythm that is characterized by rapid, uncoordinated firing of electrical impulses in the upper chambers of the heart (HEART ATRIA). In such case, blood cannot be effectively pumped into the lower chambers of the heart (HEART VENTRICLES). It is caused by abnormal impulse generation.A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain.
Alias:Auricular Fibrillation//Familial Atrial Fibrillation//Paroxysmal Atrial Fibrillation//Persistent Atrial FibrillationA-fib//AFib



Disease Association Statistics

Total Associated tsRNA Number:38
More Information
Network:
(Display the first 15 nodes)