Gene model reviewed during 5.46
Gene model reviewed during 5.55
2.8 (northern blot)
None of the polypeptides share 100% sequence identity.
608 (aa); 69 (kD predicted)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Msr-110 using the Feature Mapper tool.
Msr-110 transcript is detected in late (12-18 hr) embryos, and in larval imaginal discs. Expression in the embryo is first detected in early stage 11, in the presumptive anal plates. In late stage 11 embryos, expression is detected in the hindgut primordia, cells which will contribute to the posterior spiracle, the antenno-maxillary complex, the pharynx, the median tooth, the proventriculus, and the presumptive epidermis.
GBrowse - Visual display of RNA-Seq signalsView Dmel\Msr-110 in GBrowse 2
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 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.
Source for identity of: Msr-110 CG10596
Targets of en regulation are identified using affinity chromatography with an en containing matrix to select genomic fragments that tightly bind en. Genetic and molecular analysis of the binding sequence identifies Msr-110. Normal expression of Msr-110 is dependent upon en function.