Please see the JBrowse view of Dmel\Pur-α 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.
Multiphase exon postulated: reading frame of first coding exon differs in alternative transcripts.
Gene model reviewed during 5.43
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.47
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Pur-α 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).
Comment: maternally deposited
In early egg chambers, Pur-α is equally abundant in follicle cells and nurse cells, but as egg chambers age, it accumulates in the developing oocyte. Pur-α is a predominantly cytoplasmic protein in all cell types and developmental stages of the Drosophila ovary, but weak nuclear staining can be observed. The polar follicle cells at the anterior and posterior tip of each egg chamber show particularly strong expression.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Pur-α in JBrowse4-0
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.
monoclonal
polyclonal
Source for identity of: Pur-α CG1507