Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\hubl using the Feature Mapper tool.
hubl transcripts are detected at low levels in primary spermatocytes and are barely detected in early elongation spermatids. Robust signals are detected in more elongated spermatids at the distal ends. Transcripts localize into a ball shape at the ends of spermatids bundles, trailing away proximally to a less abundant, speckled distribution (called a comet pattern).
GBrowse - Visual display of RNA-Seq signalsView Dmel\hubl in GBrowse 2
Please Note FlyBase no longer curates genomic clone accessions so this list may not be complete
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 GBrowse 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.
Source for identity of: hubl CG30364
Source for merge of: CG30364 anon-WO0140519.168
The gene is named "hug-bell", based on the "comet"-like pattern of expression of the transcript in spermatid bundles; the mRNA localises into a ball shape at the end of the spermatid bundle, trailing away proximally to a less abundant, speckled distribution.