Tbp-1, p50, l(3)04210, Tat-binding protein-1, Pros26S-RS6A
Gene model reviewed during 5.47
There is only one protein coding transcript and one polypeptide associated with this gene
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Rpt5 using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\Rpt5 in GBrowse 2
Please Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see GBrowse for alignment of the cDNAs and ESTs to the gene model.
For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.
Source for identity of: Rpt5 Tbp-1
Source for merge of: Pros26S-RS6A CG10370
Source for merge of: Rpt5 Tbp-1
Source for merge of: Tbp-1 Pros26S-RS6A
Source for merge of: Tbp-1 anon-WO0153538.10 anon-WO0153538.8 anon-WO0153538.9
Source for merge of: Rpt5 BcDNA:GH12068
The nomenclature of genes encoding subunits of the 26S proteasome of D. melanogaster have been standardized according to FBrf0215459. These symbols/names largely follow those used already in FlyBase, and largely mirror fly community usage. HOWEVER, note that at least one other nomenclature system exists that is followed by the HUGO Gene Nomenclature Committee (HGNC), for example, with the unfortunate result that several D. melanogaster genes have shared synonyms.
Source for merge of Rpt5 Tbp-1 was sequence comparison ( date:000120 ).
Source for merge of Tbp-1 Pros26S-RS6A was sequence comparison ( date:000811 ).
Source for merge of Tbp-1 anon-WO0153538.10 anon-WO0153538.8 anon-WO0153538.9 was sequence comparison ( date:051113 ).
Source for merge of Rpt5 BcDNA:GH12068 was sequence comparison ( date:991228 ).
RNAi generated by PCR using primers directed to this gene causes a cell growth and viability phenotype when assayed in Kc167 and S2R+ cells.
RNAi screen using dsRNA made from templates generated with primers directed against this gene causes a cell growth and viability phenotype when assayed in Kc167 and S2R+ cells.