a meiosis-specific anaphase-promoting complex/cyclosome activator - functions together Fizzy to target mitotic cyclins for destruction in the egg
Please see the JBrowse view of Dmel\cort 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 5.46
Interacts with anaphase promoting complex/cyclosome (APC/C) subunits Cdc16 and Cdc27 (PubMed:18020708). Interacts with mtrm (PubMed:24019759).
Probably ubiquitinated: degraded following egg activation by the anaphase promoting complex/cyclosome (APC/C).
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\cort 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).
JBrowse - Visual display of RNA-Seq signals
View Dmel\cort in JBrowseMapping uses male recombination stimulated by P\TΔ2-3.
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.
Eggs derived from mutant females arrest in metaphase of meiosis II.
cort and grau genes are necessary for bcd protein expression. Mutations in cort impair bcd and other maternal patterning genes mRNA translation by disrupting cytoplasmic polyadenylation. bcd mRNA expression, localisation or processing are not affected. Mutations in cort do not block poly(A)-independent translational activation of nos mRNA. Phenotypic analysis demonstrates cort is required for initiation of development. Homozygous germ-line clones indicate cort is required in the germ-line. Temperature shift studies reveal cort is required at multiple stages of embryonic development.
Mutations in cort result in a maternal effect phenotype with defects during syncytial blastoderm formation.
Source for merge of: cort CG11330
Source for merge of cort CG11330 was sequence comparison ( date:010530 ).