Entry Detail



General Information

Database ID:TRD07350
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:tRF-Leu-CAG-002
tsRNA Type:tRF-3
Amino acid and Anticodon:LeuCAG
Sequence:ATCCCACTCCTGACACCA
Related Target:N/A
Predicted Target:LRRC8E//PLN//C12orf45//HERC3//C6orf89//CHST10//EML1//TADA2A//DTWD1//FGF13
External Links:
MINTbase ID:tRF-18-HRERXFD2
tRFdb ID:tRFdb-3011a

[1] gtRNAdb_ID:tRNA-Leu-CAG-1-1
Anticodon:LeuCAG
tRNA_number:trna34
Chromosome:1
Strand:+
Coordinate:Start Site(bp): 161411391        End Site(bp): 161411405+3

[2] gtRNAdb_ID:tRNA-Leu-CAG-1-2
Anticodon:LeuCAG
tRNA_number:trna36
Chromosome:1
Strand:+
Coordinate:Start Site(bp): 161418809        End Site(bp): 161418823+3

[3] gtRNAdb_ID:tRNA-Leu-CAG-1-3
Anticodon:LeuCAG
tRNA_number:trna38
Chromosome:1
Strand:+
Coordinate:Start Site(bp): 161426190        End Site(bp): 161426204+3

[4] gtRNAdb_ID:tRNA-Leu-CAG-1-4
Anticodon:LeuCAG
tRNA_number:trna40
Chromosome:1
Strand:+
Coordinate:Start Site(bp): 161433600        End Site(bp): 161433614+3

[5] gtRNAdb_ID:tRNA-Leu-CAG-1-5
Anticodon:LeuCAG
tRNA_number:trna42
Chromosome:1
Strand:+
Coordinate:Start Site(bp): 161440981        End Site(bp): 161440995+3

[6] gtRNAdb_ID:tRNA-Leu-CAG-1-6
Anticodon:LeuCAG
tRNA_number:trna67
Chromosome:1
Strand:-
Coordinate:Start Site(bp): 161500132-3        End Site(bp): 161500146

[7] gtRNAdb_ID:tRNA-Leu-CAG-1-7
Anticodon:LeuCAG
tRNA_number:trna7
Chromosome:6
Strand:+
Coordinate:Start Site(bp): 26521504        End Site(bp): 26521518+3



tsRNA Association Statistics

Total Associated Disease Number:26
More Information
Network:
(Display the first 15 nodes)



Disease Information

 MeSHDisease Ontology
Disease ID:D005909DOID:3068
Disease Name:Glioblastomaglioblastoma
Category:MeSHDisease Ontology
Type:Neoplasmsdisease of anatomical entity//disease of cellular proliferation
Define:A malignant form of astrocytoma histologically characterized by pleomorphism of cells, nuclear atypia, microhemorrhage, and necrosis. They may arise in any region of the central nervous system, with a predilection for the cerebral hemispheres, basal ganglia, and commissural pathways. Clinical presentation most frequently occurs in the fifth or sixth decade of life with focal neurologic signs or seizures.A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes.
Alias:Astrocytoma, Grade IV//Giant Cell Glioblastoma//Glioblastoma Multiformeadult glioblastoma multiforme//GBM//glioblastoma multiforme//grade IV adult Astrocytic tumor//primary glioblastoma multiforme//spongioblastoma multiforme



Disease Association Statistics

Total Associated tsRNA Number:32
More Information
Network:
(Display the first 15 nodes)