Gene model reviewed during 5.43
Gene model reviewed during 5.49
Interacts with kinesin-associated protein milt.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Miro using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\Miro 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: Miro CG5410
Miro mutant larvae exhibit severe defects in locomotion and die prematurely. Mitochondria accumulate abnormally in parallel rows in the neuronal cell body. Mutant motor nerve terminals lack mitochondria though not synaptic vesicles and cannot sustain neurotransmitter release during prolonged activity. They also lack microtubule loops and exhibit an abnormal structure: synaptic boutons are typically subdivided into numerous small synapse-bearing sub-compartments, which is likely a consequence of destabilized microtubules.