l(2)41Af, M(2)41A, M(2)S2, 41Af, l(2)EMS45-72
Gene model reviewed during 5.47
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\RpL38 using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\RpL38 in GBrowse 2
Maps close to the centromere of the second chromosome.
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.
Deletions removing RpL38 but no other cytoplasmic ribosomal protein-encoding genes show Minute phenotypes.
Identification: as a complementation group whose members dominantly modify the small wing phenotype caused by expression of Pi3K92ED954A.Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4Bx-MS1096. 2 alleles of RpL38 have been recovered.
RNAi generated by PCR using primers directed to this gene causes a cell growth and viability phenotype when assayed in Kc167 and S2R+ cells.
Transiently named CG40278 in release 3 of the genome annotation.
RpL38 has functions in wing development both acting through regulation of ct and acting independently of ct. RpL38 influences N receptro signalling or N expression during development of the wing margin, wing veins, eye and thoracic bristles.
Located close to the heterochromatic-euchromatic junction of 2R.
One of a class of genes (see MIN record) that when present in one, rather than two, copies, produce a characteristic phenotype consisting of short slender bristles and delayed development. Medium Minute. Originally identified by virtue of Minute phenotype of Df(2R)M41A10; most recurrences shown to be deficiencies. Eclosion of heterozygous deficiency delayed 13 hr (Ferrus, 1975).