Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\min 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\min in JBrowse2-90
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.
min mutants, although normal in phenotype when heterozygous or homozygous, express a phenotype indistinguishable from bb when hemizygous with deletions in the 5S rRNA region. Ordinarily, the haploid complement carries approximately 165 copies of 5S rRNA genes; in min-bearing chromosomes this number is reduced to approximately 80; according to Procunier and Tartof (1975), this number is increased by compensation to 265 in hemizygotes for the normal allele. Eclosion of min hemizygotes delayed by about two days; also show reduced viability which is more severe at 29oC than at 25oC. The relationship between min and the 5S rRNA genes is unclear, since min deletions include, not only 5S rRNA genes, but also adjacent tRNA genes. Moreover, deletions internal to the 5S rRNA array are not min (Tschudi, Pirrotta and Junakovic, 1982).
