l(4)5
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\l(4)102CDd 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\l(4)102CDd in JBrowse4-0
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.
FlyBase curator comment: The ‘l(4)102CDd’ locus was associated with 11 alleles through to FB2015_01. It was initially defined as a gene with two alleles, l(4)102CDd[1] and l(4)102CDd[2], that failed to complement each other. FBrf0226419 shows that the only extant allele, l(4)102CDd[2], is really a deletion (‘Df(4)BH’) that deletes/disrupts 10 genes, including ‘dati’. It is not known whether the original l(4)102CDd[1] allele, or other alleles in this lethal complementation group, are single lethals inside ‘Df(4)BH’ or also deletions, or whether these define one or more genes. As of FB2015_02, the ‘l(4)102CDd’ locus has been retained as a separate Gene Report, associated with 10 alleles (#1 and #3-11), while the l(4)102CDd[2] allele is now an allele of ‘dati (owing to having a break-point in ‘dati’ associated with the deletion ‘Df(4)BH’.