hrp38
Please see the JBrowse view of Dmel\Hrb98DE 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.
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.46
2.3, 1.6 (northern blot)
The group(s) of polypeptides indicated below share identical sequence to each other.
38 (kD observed)
365, 364, 361, 360 (aa)
365 (aa)
One of several protein products generated by alternative splicing.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Hrb98DE using the Feature Mapper tool.
Comment: maternally deposited
Comment: 0-20 hr AEL
Comment: 12-20 hr AEL
Comment: punctate expression in adult brain cortex
Comment: low expression throughout adult brain
GBrowse - Visual display of RNA-Seq signals
View Dmel\Hrb98DE in GBrowse 2
3-96
3-93.8
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 GBrowse 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.
monoclonal
polyclonal
Area matching Drosophila hnRNP gene Acc. No. M28870.
The consequences of HRB overexpression and absence in living flies is examined.
An Hrb98DE cDNA clone has been isolated and sequenced.
Hrb98DE has been cloned and sequenced. Eight transcripts, which can generate four protein isoforms, are produced by the use of alternative exons and splice acceptor sites.
Transcription unit defined during molecular analysis of the fkh gene region.
Isolated from a pupal cDNA library, using a fragment of the fs(1)h coding region containing "pen" repetitive sequences (GGN, where N is any nucleotide) as the probe.
A Hrb98DE cDNA has been cloned and sequenced. The predicted amino acid sequence has strong homology to a rat single-stranded nucleic acid binding protein.
This gene was also isolated by Knust et al. (1987) as a clone that cross-hybridized to a Delta probe.
