M(2)32D, L9
Please see the JBrowse view of Dmel\RpL9 for information on other features
To submit a correction to a gene model please use the Contact FlyBase form
AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Gene model reviewed during 5.50
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.55
0.8 (northern blot)
190 (aa); 21 (kD predicted)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\RpL9 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).
Comment: maternally deposited
RpL9 transcripts are detected at all stages of development on northern blots.
JBrowse - Visual display of RNA-Seq signals
View Dmel\RpL9 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.
Minute gene.
Deletions removing RpL9 but no other cytoplasmic ribosomal protein-encoding genes show Minute phenotypes.
Molecularly-defined mutations in RpL9 result in Minute phenotypes.
RNAi generated by PCR using primers directed to this gene causes a cell growth and viability phenotype when assayed in Kc167 and S2R+ cells.
The RpL9 locus encodes the ribosomal protein L9.
Source for merge of: RpL9 anon- EST:fe3A6
Source for merge of: RpL9 anon-WO0153538.25 anon-WO0153538.26 anon-WO0153538.27
Source for merge of RpL9 anon-WO0153538.25 anon-WO0153538.26 anon-WO0153538.27 was sequence comparison ( date:051113 ).
Source for identity of: RpL9 CG6141