Entry Detail



General Information

Database ID:TRD07284
Confidence:Prediction
Confidence Score:0.01 (L1-norm-Graph) & 0.01 (WBNPMD)
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics



tsRNA Information

tsRNA Name:i-tRFle-AAT-019
tsRNA Type:tRF-3
Amino acid and Anticodon:IleAAT
Sequence:TCCCCGTACGGGCCACCA
Related Target:N/A
Predicted Target:RNF39//HCLS1//LPCAT3//COL9A3//PRRC2B//NUTM2D//ALKAL2//DOK2//HLA-C//DNAH1
External Links:
MINTbase ID:tRF-18-8RSH66D2
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Ile-AAT-8-1
Anticodon:IleAAT
tRNA_number:trna57
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 27636421        End Site(bp): 27636435+3

[2] gtRNAdb_ID:tRNA-Ile-AAT-7-1
Anticodon:IleAAT
tRNA_number:trna165
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 26721221-3        End Site(bp): 26721235

[3] gtRNAdb_ID:tRNA-Ile-AAT-7-2
Anticodon:IleAAT
tRNA_number:trna28
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 26780891        End Site(bp): 26780905+3

[4] gtRNAdb_ID:tRNA-Ile-AAT-5-4
Anticodon:IleAAT
tRNA_number:trna10
Chromosome:14
Strand:+
Coordinate:Start Site(bp): 102783488        End Site(bp): 102783502+3

[5] gtRNAdb_ID:tRNA-Ile-AAT-5-5
Anticodon:IleAAT
tRNA_number:trna9
Chromosome:17
Strand:+
Coordinate:Start Site(bp): 8090970        End Site(bp): 8090984+3

[6] gtRNAdb_ID:tRNA-Ile-AAT-5-1
Anticodon:IleAAT
tRNA_number:trna11
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 26554409        End Site(bp): 26554423+3

[7] gtRNAdb_ID:tRNA-Ile-AAT-5-3
Anticodon:IleAAT
tRNA_number:trna154
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 27205350-3        End Site(bp): 27205364

[8] gtRNAdb_ID:tRNA-Ile-AAT-5-2
Anticodon:IleAAT
tRNA_number:trna158
Chromosome:6
Strand:-
Coordinate:Start Site(bp): 27144994-3        End Site(bp): 27145008

[9] gtRNAdb_ID:tRNA-Ile-AAT-1-1
Anticodon:IleAAT
tRNA_number:trna80
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 58149313        End Site(bp): 58149327+3



tsRNA Association Statistics

Total Associated Disease Number:21
More Information
Network:
(Display the first 15 nodes)



Disease Information

 MeSHDisease Ontology
Disease ID:D000077274DOID:9261
Disease Name:Nasopharyngeal Carcinomanasopharynx carcinoma
Category:MeSHDisease Ontology
Type:Neoplasms//Stomatognathic Diseases//Otorhinolaryngologic Diseasesdisease of anatomical entity//disease of cellular proliferation
Define:A carcinoma that originates in the EPITHELIUM of the NASOPHARYNX and includes four subtypes: keratinizing squamous cell, non-keratinizing, basaloid squamous cell, and PAPILLARY ADENOCARCINOMA. It is most prevalent in Southeast Asian populations and is associated with EPSTEIN-BARR VIRUS INFECTIONS. Somatic mutations associated with this cancer have been identified in NPCR, BAP1, UBAP1, ERBB2, ERBB3, MLL2, PIK3CA, KRAS, NRAS, and ARID1A genes.A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract.
Alias:N/Acarcinoma of nasopharynx//malignant Nasopharyngeal tumor//malignant neoplasm of nasopharynx//Nasopharyngeal carcinoma//nasopharynx cancer



Disease Association Statistics

Total Associated tsRNA Number:21
More Information
Network:
(Display the first 15 nodes)