l(3)10631, PM/mPM, mPM, Para, miniparamyosin
Please see the JBrowse view of Dmel\Prm 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.
Gene model reviewed during 5.46
Gene model includes transcripts encoding non-overlapping portions of the full CDS.
Gene model reviewed during 5.48
Gene model reviewed during 6.61
Heterodimer of two isoforms.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Prm 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\Prm in JBrowse3-26
3-20.9
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.
ChEST reveals this is a target of Mef2.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
Relative amounts of Prm and miniparamyosin are different in different muscle types. The pattern of Prm and miniparamyosin isoforms changes with the maturation of adult musculature. Miniparamyosin has a possible role in the sequential transition of nonfunction to functional muscle, in general, while Prm transition is more specifically related to the onset of function in thoracic flight muscles.
Prm encodes two polypeptides, paramyosin and mini-paramyosin.
Alternate promoter selection of Prm generates two polypeptides, standard paramyosin and mini-paramyosin.
The 60kD miniparamyosin isoform is encoded by the Prm gene. The 5' flanking regions of the Dvir\Prm gene and the D.melanogaster Prm gene have been sequenced and compared to try to identify any evolutionarily conserved sequences.
Source for merge of: Prm l(3)10631
Source for merge of: l(3)S010605 Prm
