l(2)k16914, L11, DL11
Please see the JBrowse view of Dmel\RpL11 for information on other features
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AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.51
0.9, 0.8 (northern blot)
184 (aa); 21 (kD predicted)
Component of the large ribosomal subunit (By similarity). Interacts with Fmr1 to form the RNA-induced silencing complex (RISC), a ribonucleoprotein (RNP) complex involved in translation regulation, other components of the complex are RpL5, Rm62, AGO2 and Dcr-1 (PubMed:12368261).
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\RpL11 using the Feature Mapper tool.
The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).
RpL11 transcripts are detected throughout development on northern blots.
JBrowse - Visual display of RNA-Seq signals
View Dmel\RpL11 in JBrowsePlease Note FlyBase no longer curates genomic clone accessions so this list may not be complete
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 JBrowse 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.
Haploinsufficient locus.
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.
Likely Minute gene.
RpL11 lies in a gap in deletion coverage.
RNAi generated by PCR using primers directed to this gene causes a cell growth and viability phenotype when assayed in Kc167 and S2R+ cells.
An RpL11 cDNA has been cloned and sequenced.
Source for merge of: RpL11 l(2)k16914
Source for merge of: RpL11 BcDNA:LD17235
"RpL11" likely corresponds to "M(2)56CD".
Source for merge of RpL11 BcDNA:LD17235 was a shared cDNA ( date:020730 ).
Source for identity of: RpL11 CG7726