M(3)67C, M(3)i, Minute, M(3)i55, M(3)RpS17
Please see the JBrowse view of Dmel\RpS17 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
Low-frequency RNA-Seq exon junction(s) not annotated.
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\RpS17 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\RpS17 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.
Likely Minute gene.
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.
A yeast phenotypic screen efficiently identifies conserved genes from more complex organisms and sheds light on their potential in vivo functions. Induced expression of RpS17 proteins causes aberrant cell shapes reflecting defects in cytokinesis and/or cel shape maintenance.
Isolated using a human ribosomal protein S17 cDNA as a probe.
RpS17 has been cloned and sequenced.
Mutant alleles have the developmental delay and bristle phenotype that makes them useful as markers in clonal analysis.
subdivisions should accompany revised localizations.
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. Moderate alleles have good heterozygous viability; extreme alleles very late eclosing <up>45 hr according to Ferrus (1975)</up> with poor viability, and females usually sterile. Viability further reduced in presence of su(f) alleles (Girton, Langner, Cejka, 1986).
Source for merge of: RpS17 BcDNA:RE44119
The genetically defined "M(3)67C" locus (characterized by previous aneuploidy analyses) likely comprises two separable, closely linked Minute genes ("RpS9" and "RpS17").
Source for merge of RpS17 BcDNA:RE44119 was a shared cDNA ( date:030728 ).
