dmiro
transmembrane Rho GTPase required for controlling anterograde transport of mitochondria and their proper distribution within nerve terminals
Please see the JBrowse view of Dmel\Miro 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 5.43
Gene model reviewed during 5.49
Interacts with kinesin-associated protein milt (PubMed:14605208, PubMed:16717129). Interacts with vimar (PubMed:27716788).
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.
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
JBrowse - Visual display of RNA-Seq signals
View Dmel\Miro in JBrowse




3-82
3-82.5
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
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.
Source for identity of: Miro CG5410