Phosphoglyceromutase, Pglym, phosphoglycerate mutase
Gene model reviewed during 5.53
1.0 (northern blot)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Pglym78 using the Feature Mapper tool.
Pglym78 transcripts are very abundant in the earliest embryonic stages. They become undetectable as embryogenesis proceeds and are detected again in 12hr embryos. During larval, pupal, and adult stages, levels rise, fall, and then rise again in a pattern similar to that of transcripts of other glycolytic genes.
GBrowse - Visual display of RNA-Seq signalsView Dmel\Pglym78 in GBrowse 2
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: Pglym78 CG1721
Characterisation of Pglym78 reveals it shares properties to other genes that encode enzymes of the glycolytic pathway: promoter region with no TATA box but multiple closely spaced transcription initiation sites and a similar expression pattern. 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.