S(rux)2B, l(2)37Dh, l(2)E1
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.44
Annotated transcripts do not represent all supported alternative splices within 5' UTR.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\swm using the Feature Mapper tool.
swm is detected at all stages of embryogenesis tested. It is present in precellularized embryos, is later enriched in the ventral midline and in segmental stripes and is ubiquitous in later embryos. It is observed in third instar larvae in imaginal discs, salivary gland, optic lobe, fat body, and in the wreath cells and gastric caecae of the gut.
GBrowse - Visual display of RNA-Seq signalsView Dmel\swm 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 merge of: l(2)37Dh S(rux)2B CG10084