Gene model reviewed during 5.39
Gene model reviewed during 5.47
There is only one protein coding transcript and one polypeptide associated with this gene
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Pglym87 using the Feature Mapper tool.
Pglym87 transcripts are detected at low levels in primary spermatocytes and are barely detected in early elongation spermatids. Robust signals are detected in more elongated spermatids at the distal ends. Transcripts localize into a ball shape at the ends of spermatids bundles, trailing away proximally to a less abundant, speckled distribution (called a comet pattern).
GBrowse - Visual display of RNA-Seq signalsView Dmel\Pglym87 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.
Comparison of the gene structure of Pglym78 and Pglym87 suggests that Pglym87 arose through retrotransposition from a Pglym78 transcript, additional more complex mechanisms may have played some role in the origin of Pglym87. Structural properties suggest Pglym87 is a pseudogene with a peculiar rate and pattern of evolution, aspects of Pglym87 molecular evolution suggest it might be a functional gene having puzzling aspects in its structure.