Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\M(2)58F using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\M(2)58F in GBrowse 2
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.
The genetically defined "M(2)58F" locus (characterized by previous aneuploidy analyses) likely comprises two separable, closely linked Minute genes ("RpS16" and "RpS24").
"M(2)58F" may correspond to "RpL17A".
Location of M(2)58F similar to the location of RpL17A.
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. Identified by the strong Minute phenotype of Df(2R)M58F. Heterozygosity for null allele as represented by the deficiency characterized by a two-day delay in eclosion (at 25oC) owing to delay in puparium formation (Dunn and Mossige, 1937); delay 19 hr according to Ferrus (1975).