Entry Detail



General Information

Database ID:TRD08676
Confidence:Prediction
Confidence Score:0.01 (L1-norm-Graph) & 0.03 (WBNPMD)
Contents:>> tsRNA Information
>> tsRNA Association Statistics
>> Disease Information
>> Disease Association Statistics



tsRNA Information

tsRNA Name:tRF-28-PSQP4PW3FJD0
tsRNA Type:tRF-5
Amino acid and Anticodon:LysCTT
Sequence:GCCCGGCTAGCTCAGTCGGTAGAGCATG
Related Target:N/A
Predicted Target:EBI3//RPS6KA2//RPS6KA1//RHOD//PIK3CD//ACAN//FBXL12//PRPF40B//B3GNT4//NMT1
External Links:
MINTbase ID:tRF-28-PSQP4PW3FJD0
tRFdb ID:N/A

[1] gtRNAdb_ID:tRNA-Lys-CTT-4-1
Anticodon:LysCTT
tRNA_number:trna10
Chromosome:16
Strand:+
Coordinate:Start Site(bp): 3241501        End Site(bp): 3241528

[2] gtRNAdb_ID:tRNA-Lys-CTT-3-1
Anticodon:LysCTT
tRNA_number:trna32
Chromosome:16
Strand:-
Coordinate:Start Site(bp): 3207451        End Site(bp): 3207478

[3] gtRNAdb_ID:tRNA-Lys-CTT-2-1
Anticodon:LysCTT
tRNA_number:trna119
Chromosome:1
Strand:-
Coordinate:Start Site(bp): 145395567        End Site(bp): 145395594

[4] gtRNAdb_ID:tRNA-Lys-CTT-2-5
Anticodon:LysCTT
tRNA_number:trna7
Chromosome:16
Strand:+
Coordinate:Start Site(bp): 3225692        End Site(bp): 3225719

[5] gtRNAdb_ID:tRNA-Lys-CTT-2-3
Anticodon:LysCTT
tRNA_number:trna11
Chromosome:5
Strand:-
Coordinate:Start Site(bp): 180649024        End Site(bp): 180649051

[6] gtRNAdb_ID:tRNA-Lys-CTT-2-2
Anticodon:LysCTT
tRNA_number:trna9
Chromosome:5
Strand:+
Coordinate:Start Site(bp): 180634755        End Site(bp): 180634782

[7] gtRNAdb_ID:tRNA-Lys-CTT-2-4
Anticodon:LysCTT
tRNA_number:trna13
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 26556774        End Site(bp): 26556801

[8] gtRNAdb_ID:tRNA-Lys-CTT-1-1
Anticodon:LysCTT
tRNA_number:trna13
Chromosome:14
Strand:-
Coordinate:Start Site(bp): 58706658        End Site(bp): 58706685

[9] gtRNAdb_ID:tRNA-Lys-CTT-1-2
Anticodon:LysCTT
tRNA_number:trna2
Chromosome:15
Strand:+
Coordinate:Start Site(bp): 79152904        End Site(bp): 79152931



tsRNA Association Statistics

Total Associated Disease Number:33
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)