CT6940
Please see the JBrowse view of Dmel\nolo 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.
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
Gene model reviewed during 5.49
Multiphase exon postulated: exon reading frame differs in alternative transcripts; overlap >20aa.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\nolo 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: reported as larval eye primordium
JBrowse - Visual display of RNA-Seq signals
View Dmel\nolo in JBrowse




2-54
2-54.6
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.
Source for merge of: CG2131 CG2122
Source for merge of: CG13236 CG2131
Annotations CG13236, CG2122 and CG2131 merged as CG31619 in release 3 of the genome annotation.
Source for merge of CG2131 CG2122 was a shared cDNA ( date:010720 ).
Source for identity of: nolo CG31619
Named 'no long nerve cord' because the length of the ventral nerve cord is not extended in mutants, whereas initial experiments using RNAi to knock-down expression of the gene id produce this phenotype.