Mitch, BcDNA:LD37196 , l(3)S3, S3, chromosome alignment defect 2
Please see the JBrowse view of Dmel\Spc25 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 5.48
There is only one protein coding transcript and one polypeptide associated with this gene
Component of the Ndc80 complex, which is composed of Ndc80, Nuf2 and Spc25.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Spc25 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
Subcellular localization to kinetochores of embryonic mitotic cells assayed using the transgenic allele Spc25T:AvicGFP-EGFP.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Spc25 in JBrowsePlease 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.
RNAi screen using dsRNA made from templates generated with primers directed against this gene results in chromosome misalignment on the metaphase spindle and a spindle that is aberrantly long when assayed in S2 cells. This phenotype can be observed when the screen is performed with or without Cdc27 dsRNA.
Source for merge of: BcDNA:LD37196 CG7242
Source for merge of: CG7242 l(3)87Da
Source for identity of: Spc25 CG7242
Named "chromosome alignment defect 2" after the observed cellular phenotype following treatment of S2 cells with cal2 dsRNA.
The gene is named "mitotic chaos" after the mutant phenotype.