BACK (BTB and C-terminal Kelch) domain protein - a mediator of axon death - axed mutants suppress axon death - acts in glia downstream of sarm - pro-degenerative pathways activated by Sarm signaling or Nmnat elimination ultimately converge on Axed - possibly involved in recruitment of substrates to Cullin Ring Ubiquitin Ligase complexes B
Please see the JBrowse view of Dmel\axed for information on other features
To submit a correction to a gene model please use the Contact FlyBase form
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 5.44
Gene model reviewed during 5.46
Stop-codon suppression (UGA) postulated; FBrf0216884, FBrf0234051.
Gene model reviewed during 6.25
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\axed 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\axed in JBrowse
3-17
3-15.2
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 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.
Source for merge of: CG8398 anon- EST:Posey31
Source for identity of: axed CG8398
The gene is named 'axundead' based on the phenotype of long-term survival of severed axons that should otherwise undergo axon death.