ARD, Dβ1, nAcRβ-64B, nAChR, nAcRbeta-64B
Please see the JBrowse view of Dmel\nAChRβ1 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
7.5, 4.2, 3.2 (northern blot)
2.418 (longest cDNA)
3.0 (northern blot)
None of the polypeptides share 100% sequence identity.
521 (aa)
nAcRα-96Aa protein appears to be the
ligand-binding subunit of the class I α-Btx binding complex.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\nAChRβ1 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\nAChRβ1 in JBrowse3-12
3-9.7
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 a 900bp genomic promoter fragment contains the essential information for correct temporal and spatial expression.
A potential non-alpha subunit.
Ecol\lacZ reporter gene constructs have been used to identify one region necessary for transcriptional regulation of this subunit. nAcRβ-64B encodes a structural homologue of vertebrate nicotinic acetylcholine receptors (nAChR). Fusion constructs containing regions of the nAcRβ-64B were used to investigate the relationship between the nAcRβ-64B gene product and α-bungarotoxin binding sites. Equilibrium binding and kinetic studies reveal two different high affinity binding sites for α-bungarotoxin in fly head membranes.
Excitatory nAcRβ-64B gene product is encoded by a superfamily of related genes.
RNA blot hybridizations found a 3kb poly A transcript complementary to nAcRβ-64B during midembryogenesis, metamorphosis and in newly enclosed adults.
Source for merge of: CG12606 CG11348
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.
"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).
Source for merge of CG12606 CG11348 was a shared cDNA.
Source for identity of: nAChRβ1 nAcRβ-64B
Renamed genes encoding nicotinic Acetylcholine Receptors to give systematic nomenclature that better reflects usage in literature (e.g. FBrf0218556, FBrf0183743).