Paired-like homeobox transcription factor - mutants are embryonic lethal and characterized by a reduction in the anterior protocerebrum, including the mushroom bodies, and a loss of the supraoesophageal brain commissure - in larvae expressed in all type II lineages and the optic lobes including the medulla and lobula plug - mutants are characterized by a reduction of the protocerebrum, a loss of the supraesophageal commissure and mushroom body progenitors and also by a dislocation of the optic lobes - Homeobrain define middle-aged and late intermediate neural progenitor temporal windows and play a role in cellular longevity - Homeobrain has conserved functions as temporal factors in the developing visual system
Please see the JBrowse view of Dmel\hbn for information on other features
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AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Gene model reviewed during 5.51
There is only one protein coding transcript and one polypeptide associated with this gene
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\hbn 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).
Comment: maternally deposited
Comment: anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
hbn transcript expression begins at embryonic stage 4 as a U-shaped pattern in the dorsal head region. During embryonic stage 5 the hbn expression domain retracts from the ventro-lateral side of the presumptive head. A second hbn expression domain, dorso-lateral to the first domain, becomes visible on each side of the embryo during embryonic stages 6-7, and the U-shaped pattern resolves into two distinct domains, a weakly-expressed dorsal domain and a strongly-expressed dorso-lateral domain. During embryonic stages 9-10, transcript expression is detected in three domains on each side of the dorsal posterior head and in a dorsal-anterior spot. When the germband is fully extended at stage 11, a few cells in each neuromere of the ventral nerve cord express hbn transcript. Shortly afterwards each of the three dorso-lateral expression domains in the head split, resulting in six dorso-lateral patches of expression. hbn transcript is expressed in the developing hindgut at the boundary with the midgut during germband retraction. Discrete localized expression domains in the brain and in the ventral nerve cord are detected until the end of embryogenesis.
hbn is expressed in subsets of neuroblasts in stage 16 embryos. It is also observed in mushroom body neuroblasts. In type II neuroblasts, it is expressed in the PDM and DL clusters. It is also expressed in many type 1 neuroblasts.
JBrowse - Visual display of RNA-Seq signals
View Dmel\hbn in JBrowse2-92
2-99.5
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 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.
polyclonal
RNAi generated by PCR using primers directed to this gene causes a cell growth and viability phenotype when assayed in Kc167 and S2R+ cells.
An incompletely characterised homeodomain sequence.
Annotations CG10614, CG15647, CG15648 merged as CG33152 in release 3 of the genome annotation.
Source for identity of homeobrain CG10614 CG15647 was sequence comparison ( date:000915 ).
Source for identity of: homeobrain CG10614 CG15647