l(2)144/1, l(2)k14401, oho-31
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\oho31 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\oho31 in JBrowsePlease 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.
Mutants isolated in a screen of the second chromosome identifying genes affecting disc morphology.
Mutants display an imaginal disc and blood cell neoplastic phenotype.
The larval lethality and overgrowth of hematopoietic tissue phenotypes originally described as being due to Penk14401a in FBrf0082252 and FBrf0082712 have been found to be due to a second site mutation (oho31k14401b).
FlyBase curator comment: "oho31" phenotype (overgrown hematopoietic tissues and larval lethality) in the "l(2)k14401" insertion line is stated in FBrf0082252 to be due to an effect on the "Pen" gene, however, FBrf0149010 states that the "oho31" mutant phenotype is caused by a second site mutation separable from the insertion in "Pen" in the "l(2)k14401" insertion line.
FlyBase curator comment: "oho31" phenotype (overgrown hematopoietic tissues and larval lethality) in the "l(2)k14401" insertion line is stated in FBrf0082712 to be due to an effect on the "Pen" gene, however, FBrf0149010 states that the "oho31" mutant phenotype is caused by a second site mutation separable from the insertion in "Pen" in the "l(2)k14401" insertion line.