nebula, nla, 89B11, l(3)05203
regulates female meiosis by controlling calcineurin activity in the germline - exacerbates Aβ42 phenotypes in a Drosophila model of Alzheimer's disease
Please see the JBrowse view of Dmel\sra 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.
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.54
Interacts with Pp2B-14D, CanA-14F and CanB2.
Phosphorylation at Ser-215 and Ser-219 is essential for calcineurin activation and completion of female meiosis. Sgg is required for phosphorylation of Ser-215 in activated eggs. Ser-100, Thr-102 and Ser-219 are highly phosphorylated in both ovaries and activated eggs; however, phosphorylation at Ser-100 or Thr-102 is not required for sra function in completion of female meiosis.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\sra 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\sra in JBrowse

3-58
3-58.2
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 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.
Mutant females show spontaneous ovulation as virgins, sterility with impaired meiotic progression and compromised postmating responses, with a lower ovulation level, higher remating rate and shorter period for restoration of receptivity.
Area matching Drosophila EST AA979551. This EST overlaps EST AA567400.
Identification: Enhancer trap screen designed to discover genes involved in the cellular aspects of defense mechanisms, as well as in melanotic tumor formation processes linked to blood cell disregulation.
Mutations of sra affect oviposition.
The autosomal "FLP-DFS" technique (using the P{ovoD1-18} P{FRT(whs)} P{hsFLP} chromosomes) has been used to identify the specific maternal effect phenotype for the zygotic lethal mutation. l(3)05203 gene expression during oogenesis is not critical to embryonic development, but the gene function may be essential for fertilisation and/or completion of meiosis.
Source for merge of: sra nla
Source for merge of: sra l(3)05203
Source for merge of: sra anon-WO0118547.92 anon-WO0172774.10
l(3)L1820 may correspond to sra: the P{lacW}l(3)L1820L1820 insertion maps within the transcription unit.
The relationship between "fey" and "sra" is unclear. It is possible that "fey" is a lethal "sra" allele.
"sra" is a distinct gene from "Sb".
Source for merge of sra anon-WO0118547.92 anon-WO0172774.10 was sequence comparison ( date:051113 ).
Gene name is "Sarah" because Sarah, Abraham's wife, was infertile for many years but eventually had a child. This is also the fate of homozygous sraA381 females.