Glu
Please see the JBrowse view of Dmel\βGlu 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 5.49
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.40
3.6 (northern blot)
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\βGlu 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\βGlu in JBrowsePlease 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.
May or may not be a structural gene for β-D-Glucuronidase. The enzyme is a glycoprotein and exists in two chromatographically separable forms. Form I is membrane bound, has a pI of 8.0 - 8.5 and can be irreversibly inactivated by either incubation at 55oC for 20 min or by incubation at 37oC in the presence of 6M urea; form II exists in both membrane-bound and free states, has a pI of 4.5 and is resistant to inactivation by the above treatments. The two are kinetically similar, having similar Km and Vmax and are precipitated by antibody raised against form II.
Source for merge of: Glu CG2135
'Glu' ('β glucuronidase') was a non-sequenced localized gene mapping to 98F1-100F5. Gene Ontology analysis and ortholog analysis agree there are two Dmel genes encoding β glucuronidases: 'CG2135' (100D2) and 'CG15117' (56B5). These data indicate that the 'Glu' gene is identical to the 'CG2135' annotation.
Source for identity of: βGlu Glu
The original 'Glu' symbol for 'β glucuronidase' has been changed to 'βGlu' to (i) better match the fullname, (ii) reflect the symbol used in the original paper characterizing the enzyme (FBrf0039685), and (iii) minimize confusion with the unrelated 'glu' gene.