Dα2, SAD, nAcRα-96Ab, nAChR, Da2
Please see the JBrowse view of Dmel\nAChRα2 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 5.47
2.385 (compiled cDNA)
2.5 (northern blot)
2.6 (northern blot)
The group(s) of polypeptides indicated below share identical sequence to each other.
576 (aa); 61 (kD)
576 (aa)
576 (aa); 61 (kD predicted)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\nAChRα2 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
Comment: anlage in statu nascendi
Comment: anlage in statu nascendi
Comment: reported as plasmatocytes anlage
JBrowse - Visual display of RNA-Seq signals
View Dmel\nAChRα2 in JBrowse





3-85
3-83.8
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.
Ecol\lacZ reporter gene constructs demonstrate the nAcRα-96Ab promoter is complex. A 1.23kb genomic promoter harbours the essential cis-elements for basic expression. Additional enhancer elements for strong expression in the optic lobe tangential cells are located 1.7 to 7.3kb upstream of the transcription start site.
Promoter region of nAcRα-96Ab is dissected and functional regions are identified.
Ecol\lacZ reporter gene constructs have been used to identify at least two elements necessary for regulated expression. One element is a 350bp region 1kb upstream of the putative transcription start site and contains a 37bp element that has high homology to element A2 of Ddc enhancer (Johnson et al, Genes and Devel. 3: 676).
The predicted mature protein contains 535 amino acid residues and an Mr of 60,963. It has an unusually long signal sequence of 41 residues.
The structure and developmental expression of Acr96Ab, a member of the nAChR gene family, has been characterized.
Northern blot analysis was used to determine the developmental expression of Acr96Ab and in situ hybridization revealed localization of Acr96Ab in the embryonic CNS.
nAcRα-96Ab appears to be a chimeric gene, with the 5' part of the gene derived from nAcRα-96Aa and the 3' part of the gene derived from nAcRβ-64B.
mir-1017 is a 3' tailed mirtron produced from an intron of nAcRα-96Ab.
"nAcRα-96Ab" is a putative chimeric gene derived from the "nAcRα-96Aa" and "nAcRβ-64B" genes (where coding sequences of the two parental genes contribute to the coding sequence of the chimeric gene).
The potential miRNA mir-1017 is located in an intron of nAcRα-96Ab.
Source for identity of: nAcRα-96Ab CG6844
Source for identity of: nAChRα2 nAcRα-96Ab
Renamed genes encoding nicotinic Acetylcholine Receptors to give systematic nomenclature that better reflects usage in literature (e.g. FBrf0218556, FBrf0183743).