l(1)ts403, NXF1, DmNXF1, nuclear export factor 1, NFX1
Please see the JBrowse view of Dmel\sbr 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.
Gene model reviewed during 5.45
Gene model reviewed during 6.19
Interacts with Nxt1 (PubMed:11780633, PubMed:31570835). Interacts with ZC3H3 (PubMed:19364924). Forms a complex with Nup358/RanBP2, RanGAP and Nxt1 (PubMed:14729961). Interacts with Nup54 and Nup58 (PubMed:33856346). Interacts with Orc3 and Hpr1 (PubMed:27016737).
The leucine-rich repeats and the NTF2-domain are essential for the export of mRNA from the nucleus.
The C-terminal fragment, containing the TAP domain (also called UBA-like domain) and part of the NTF2-like domain, named the NPC-binding domain, mediates direct interactions with nucleoporin-FG-repeats and is necessary and sufficient for localization of NXF1 to the nuclear rim.
The RNA-binding domain is a non-canonical RNP-type domain.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\sbr 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: ovaries included
Comment: testes included
JBrowse - Visual display of RNA-Seq signals
View Dmel\sbr in JBrowse1-33
1-33.8
1-32.82
1-32.53--32.67
1-32.8
No crossovers with ras in 669 flies.
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.
polyclonal
RNAi generated by PCR using primers directed to this gene causes a cell growth and viability phenotype when assayed in Kc167 and S2R+ cells.
Depletion of sbr in SL2 cells (using RNAi) inhibits cell growth and results in a rapid and robust accumulation of polyadenylated RNAs within the nucleus.
Neurons show pathfinding defects and body wall muscles have defective morphology in mutant embryos. Mutant adults have smaller and thinner bristles than normal with a reduced diameter.
Candidate gene for cyst length quantitative trait locus.
Most alleles homozygous and hemizygous lethal.
Source for merge of: sbr CG1664
Source for merge of sbr CG1664 was Swiss-Prot update ( date:020819 ).