essential for enterocyte differentiation from enteroblast in the midgut - involved in feedback amplification loop that leads to rapid production from intestinal stem cells of differentiation-defective enteroblasts and subsequent tumorigenesis - Sox100B directly regulates Sox21a to promote differentiation - Sox21a and GATAe form a functional relay to orchestrate EB differentiation - genetic interaction between peroxisomes and the JAK and STAT signaling restores the expression defect of Sox21a in peroxisome defective cells
Please see the JBrowse view of Dmel\Sox21a 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 5.44
Stop-codon suppression (UGA) postulated; FBrf0216884..
Gene model reviewed during 5.46
None of the polypeptides share 100% sequence identity.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Sox21a 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
Sox21a appears to be preferentially expressed in differentiating enteroblasts in the midgut epithelium. It is not detected in newly eclosed adults. Weak expression is observed in enteroblasts and intestinal stem cells of the midgut epithelium at 5 days and it increases with age. Expression is higher in enteroblasts than in intestinal stem cells.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Sox21a in JBrowse3-42
3-35.6
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
S2 cells treated with dsRNA generated against this gene show reduced phagocytosis of Candida albicans compared to untreated cells.
Source for merge of: Sox21a SoxB2.3
Source for identity of: Sox21a CG7345