s38, s38-1
Please see the JBrowse view of Dmel\Cp38 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 5.45
Gene model reviewed during 5.52
1.4 (northern blot)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Cp38 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: minus midline cells
The six major chorion bands are dramatically reduced in follicles of Mcm6K1214, mus101K451 and fs(1)A1059K1 mutants. No reduction of major chorion bands is seen in swa6 although some affects are seen in higher molecular weight components.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Cp38 in JBrowse1-23
1-23.4
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.
In a sample of 79 genes with multiple introns, 33 showed significant heterogeneity in G+C content among introns of the same gene and significant positive correspondence between the intron and the third codon position G+C content within genes. These results are consistent with selection adding against preferred codons at the start of genes.
Primarily regulated at the transcriptional level.
mus101K451, Mcm6K1214 and fs(1)A1059K1 mutants interfere with the amplification of the major chorion genes Cp15, Cp16, Cp18, Cp19, Cp36 and Cp38.
Tissue and stage specific expression of Cp15 and Cp38 are retained when the genes are removed from the remaining genes of the cluster, and in the absence of amplification. Deletion analysis has delimited sequences regulating Cp38 transcription to within a portion of its upstream spacer and 5' transcribed region.
Structural gene for s38-1, a 38,000-dalton chorion protein. Synthesis primarily during stages 12 and 13 (Waring and Mahowald) and during stages 11 and 12 (Petri, Wyman and Kafatos, 1976). 2,000 to 3,000 daltons cleaved from primary translation product to yield mature protein (Spradling, Digan, Mahowald, Scott and Craig, 1980). Temporal and spatial distribution of expression described by Parks and Spradling (1987).