Alternative translation stop created by use of multiphasic reading frames within coding region.
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.52
None of the polypeptides share 100% sequence identity.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\osp using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\osp 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: osp CG3479
Source for merge of: osp anon-WO02059370.75
" BG:DS09219.1 " is located within osp and is predicted to be transcribed in the same direction as osp. It may therefore be part of the osp gene, if osp has an alternative transcript that has not yet been identified as a cDNA.
Source for merge of osp anon-WO02059370.75 was sequence comparison ( date:051113 ).
Since "osp" is very near the 2L breakpoint of T(2;3)Mpe, the "Mpe1" phenotype may be due to a dominant "osp" allele.
Allelism of osp and alw assumed on basis of phenotype and map position (Ashburner).