Dank1
Please see the JBrowse view of Dmel\Ank 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 supported alternative splices within 5' UTR.
Gene model reviewed during 5.46
Gene model reviewed during 5.47
Tissue-specific extension of 3' UTRs observed during later stages (FBrf0218523, FBrf0219848); all variants may not be annotated
5.5 (northern blot)
1549 (aa); 170 (kD observed); 170 (kD predicted)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Ank 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).
Ank transcripts are detected in RNA from ovaries and embryos.
Ank is expressed at the lateral cell contacts of follicle cells in the ovary.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Ank in JBrowse4-0
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.
Ank is not required for the recruitment of Spectrin to postsynaptic muscle membranes at the neuromuscular junction.
Ank contributes to the Spectrin-dependent control of synapse development.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
The Ank gene product is a component of spectrosomes but not fusomes.
Ank was identified by amplification of genomic DNA with oligonucleotide primers based on a conserved region of mammalian brain ankyrin.
Source for identity of: Ank CG1651