Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated transcripts do not represent all supported alternative splices within 5' UTR.
Gene model reviewed during 5.50
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Pkcδ using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\Pkcδ 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.
The phosphorylation state and ATPase activity of myosin light chain isoforms has been compared in wild-type and mfd- flies.
Deletion of salivary segment 11A6-7 leads to inability to jump or fly, hemizygosity for this variant allows viability and the phenotypic defects induced by the deletion are recessive; myofibrils or thoracic muscles shortened; spots are missing in two dimensional gel analysis of proteins from fibrillar and tubular muscles; these differences from wild type apparently due to blocking of phosphorylation of proteins in these muscles; such proteins are very likely myosins that become phosphorylated during the first day after eclosion (in wild-type), in parallel with the gradual development of flying and jumping ability (Hiromi, Ohmura, Masaki, Hirose and Hotta).