Gene model reviewed during 5.43
Gene model reviewed during 5.52
Annotated transcripts do not represent all supported alternative splices within 5' UTR.
0.95 (northern blot)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\RpL13 using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\RpL13 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 merge of: RpL13 anon- EST:fe1D1
The genetically defined "M(2)31A" locus (characterized by previous aneuploidy analyses) likely comprises two separable, closely linked Minute genes ("RpL7" and "RpL13").
RNAi screen using dsRNA made from templates generated with primers directed against this gene results in aberrantly short, monopolar spindles when assayed in S2 cells. This phenotype can be observed when the screen is performed with or without Cdc27 dsRNA.
dsRNA made from templates generated with primers directed against RpL13 that is transfected into S2 treated with Listeria monocytogenes reveals RpL13 to be involved in Listeria monocytogenes vacuolar escape.