sda, slamdance
Please see the JBrowse view of Dmel\CG46339 for information on other features
To submit a correction to a gene model please use the Contact FlyBase form
AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
Gene model reviewed during 6.17
The group(s) of polypeptides indicated below share identical sequence to each other.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\CG46339 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\CG46339 in JBrowse3-92
3-89.3
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.
The gene corresponding to the CG5518 annotation was named 'sda, slamdance', based mainly on the bang sensitive phenotypes associated with sda[iso7.8] (FBal0060899), described in FBrf0083354 and FBrf0155803. However, FBrf0235003 presents evidence that FBal0060899 instead maps to CG14509. Thus in FB2017_04, FBal0060899 and other unmapped alleles with bang sensitive phenotypes have been moved to CG14509, while those alleles and insertions mapping molecularly to the CG5518 annotation are retained with this gene. The CG5518 annotation has been renamed to CG46339 to avoid confusion.