Gene model reviewed during 5.55
Gene model reviewed during 5.46
Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated as dicistronic; possible double stop-codon readthrough.
Gene model reviewed during 6.05
None of the polypeptides share 100% sequence identity.
Interacts with osk.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Lasp using the Feature Mapper tool.
Lasp protein is detected in region 2 and in two cells (probably cap cells) at the anterior tip of the germarium. During mid-oogenesis, Lasp is abundant in nurse cells and in the oocyte. It is mildly enriched at the posterior end of the oocyte, is found in anterior and posterior polar follicle cells and is present on ring canals. At stage S10, it is detected at nurse cell borders, in ring canals and around the cortex of the oocyte. In preblastoderm embryos, it is observed at the posterior pole.
GBrowse - Visual display of RNA-Seq signalsView Dmel\Lasp 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.
Source for merge of anon-73Bd Lasp was comparison of molecular map data with genome ( date:031008 ).
Source for merge of Lasp CG3849 was sequence comparison ( date:030120 ).