Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Phox 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\Phox in JBrowse2-80.6
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 molecular weight of Phox is 54kD, which differs from the weight reported for proPO-A1 in FBrf0027149.
The "Phox, Phenol oxidase" gene originally described in FBrf0034818 had been merged with the proPO-A1 gene (and thus with the Black cells (Bc) mutation) in FlyBase. This is probably because in FBrf0064348 it is suggested that Phox may be the same locus as proPO-A1, since it maps to the same location and both proPO-A1 and Phox show monophenol oxidase activity. However, FBrf0036109 determined the molecular weight of Phox to be 54kD, which differs from the weight reported for proPO-A1 in FBrf0027149. Thus the "Phox, Phenol oxidase" gene originally described in FBrf0034818 has been split out into a separate gene in its own right in FlyBase in release FB_2009_09.
"Phox" may correspond to "proPO-A1", since they map to the same location and both show monophenol oxidase activity.
It is unlikely that Phox corresponds to proPO-A1 (the A1 component of phenol oxidase described in FBrf0017315).