l(2)41Af, M(2)41A, M(2)S2, l(2)EMS45-72, 41Af
Please see the JBrowse view of Dmel\RpL38 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.
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.
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).
JBrowse - Visual display of RNA-Seq signals
View Dmel\RpL38 in JBrowse2-55
2-55.3
2-55.1
Maps close to the centromere of the second chromosome.
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 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.
Minute gene.
Deletions removing RpL38 but no other cytoplasmic ribosomal protein-encoding genes show Minute phenotypes.
Molecularly-defined mutations in RpL38 result in 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.
Stated to fall into the same Group IV complementation group as l(2)41Ae.
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).
Source for merge of: RpL38 l(2)41Af M(2)41A
Source for merge of: CG18001 BcDNA:RE42506