l(1)zw10, mit(1)15, EG:BACR7C10.3 , zw-10, abnormal-eye
a subunit of the RZZ complex located at the kinetochores of chromosomes - the RZZ complex plays an essential role in the spindle assembly checkpoint that ensures proper connections between chromosomes and the mitotic spindle. - found on the Golgi stacks and endoplasmic reticulum where it functions in membrane formation and trafficking.
Please see the JBrowse view of Dmel\Zw10 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 5.47
Gene model reviewed during 5.50
2.6 (northern blot)
There is only one protein coding transcript and one polypeptide associated with this gene
721 (aa); 85 (kD observed)
Component of the RZZ complex composed of rod, Zw10 and Zwilch.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Zw10 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: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Levels of mit(1)15 transcript are high in embryos and in adult females, decline in first and second instar larvae, and increase again in third instar larvae and in early pupae.
Comment: reference states 0-16 hr AEL
A 85 kD band was observed in Western blots of protein from 0-16 hr embryos, third instar larvae, and Schneider 2 cell lines. The subcellular localization of mit(1)15 protein changes during mitosis in syncytial blastoderm embryos.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Zw10 in JBrowse



1-1
1-1.1
1-1.2
1-1.2 +/- 0.4
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.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
RNAi screen using dsRNA made from templates generated with primers directed against this gene causes a phenotype when assayed in S2R+ cells: cell morphology is aberrant, indicative of a failure in cell cycle/mitosis progression. This phenotype is not seen in Kc167 cells.
Candidate gene for testis length quantitative trait locus.
mit(1)15 can localise to mini-chromosomes that contain the fully functional centromere and to acentric mini-chromosomes that contain only 225-290kb of sub-telomeric DNA.
Homologs of mit(1)15 identified by sequence similarity are identified.
mit(1)15 is required for proper chromosome segregation during both meiotic divisions. Function in chromosome segregation must affect both separation of sister chromatids (during mitosis and meiosis II) and the separation of homologous chromosomes (during meiosis I).
High levels of meiotic nondisjunction due to delay of chromosome migration to the poles at anaphase. Also there is a high frequency of cytokinesis failure.
Mutations in mit(1)15 can cause essentially random mitotic segregation of chromosomes.
Based on map position and phenotype mit(1)15 is thought to be synonymous with abe.
One of a group of fourteen loci identified as temperature-sensitive lethal mutations (Baker) that exhibit, at semirestrictive temperatures, elevated frequencies of clones of homozygous mwh cells in the wings of surviving mit(1);mwh/+ males and of y clones and y//mwh twin spots in the abdomens of y mit(1); T(1;3)scJ4, y+ mwh/+ males. The presence of large clones is consistent with origin via mitotic exchange, mitotic nondisjunction of both homologues, or mutation; twin spots are not expected to result from somatic mutation; only mitotic nondisjunction produces y Sb+ clones in T(1;3)scJ4, y+ Sb/+. Preponderance of small clones suggests origin via chromosome breakage.
Source for merge of: mit(1)15 CG9900
inter se allelism tests have not been performed.
Source for identity of: Zw10 mit(1)15
Renamed to 'Zw10' to replace the placeholder symbol 'mit(1)15' and to better reflect usage in the literature.