Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Frd 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\Frd in JBrowse2-102.4
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 Frd complementation group corresponds to one (or more) of the following annotated genes: CG42741, CG44252, CG44253, DCTN3-p24, CG9890, PPO3 (this mapping is based on the recessive lethality of the Frd1 chromosome). Frd may correspond to PPO3: FBrf0240659 shows that Frd1 mutants carry an intragenic deletion in PPO3.
The Frd1 allele is associated with an 11bp deletion in the coding domain of a prophenoloxidase that maps to the genetic interval (59C) where the Frd complementation group maps.