L22, eRpL22, EG:BACR19J1.4
Please see the JBrowse view of Dmel\RpL22 for information on other features
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Gene model reviewed during 5.50
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\RpL22 using the Feature Mapper tool.
Comment: maternally deposited
RpL22 is ubiquitously expressed in the adult male reproductive system.
GBrowse - Visual display of RNA-Seq signals
View Dmel\RpL22 in GBrowse 21-0
1-0
1-0.0
Please 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 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.
polyclonal
Source for identity of: RpL22 CG7434
"l(1)G0451" may affect "RpL22". "l(1)G0115" may affect "RpL22". "l(1)G0422" may affect "RpL22".
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.
Not a Minute gene.
Deletions removing RpL22 but no other cytoplasmic ribosomal protein-encoding genes do not show Minute phenotypes.
Molecularly-defined mutations in RpL22 do not 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.
Identification: Protein that interacts with the AM domain of Parp protein.