Please see the JBrowse view of Dmel\Nuf2 for information on other features
To submit a correction to a gene model please use the Contact FlyBase form
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
There is only one protein coding transcript and one polypeptide associated with this gene
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Nuf2 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).
Subcellular localization to kinetochores of embryonic mitotic cells assayed using the transgenic allele Nuf2T:AvicGFP-EGFP.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Nuf2 in JBrowse2-24
2-23.2
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.
RNAi screen using dsRNA made from templates generated with primers directed against this gene results in chromosome misalignment on the metaphase spindle and a spindle that is aberrantly long when assayed in S2 cells. This phenotype can be observed when the screen is performed with or without Cdc27 dsRNA.
3 alleles of CG8902 recovered in a P-insertion screen.
Area matching Drosophila ESTs AA801691 and AA441008. Probable intron in gene represented by EST AA801691.
Source for merge of: CG8902 anon-WO0118547.214
Source for merge of CG8902 anon-WO0118547.214 was sequence comparison ( date:051113 ).
Source for identity of: Nuf2 CG8902