BG:DS01486.7
Please see the JBrowse view of Dmel\osp for information on other features
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AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
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.
The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).
JBrowse - Visual display of RNA-Seq signals
View Dmel\osp in JBrowseMaps very near b.
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 JBrowse 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.
osp is not a vital gene.
Source for merge of: osp anon-WO02059370.75
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).
Source for identity of: osp CG3479