Please see the JBrowse view of Dmel\Vha100-2 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
Annotated transcripts do not represent all supported alternative splices within 5' UTR.
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.55
The group(s) of polypeptides indicated below share identical sequence to each other.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Vha100-2 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: reported as anal pad specific anlage
Comment: enriched in acidic region
RNA-seq data show that Vha100-2 is expressed in the gastric caecum and throughout the larval midgut but is enriched in the acidic region of the midgut.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Vha100-2 in JBrowse3-63
3-62.5
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.
Area matching Drosophila EST AA202297. This EST has sequence similarity to vacuolar ATPase genes.
Source for merge of: BcDNA:LD21735 CG18617 CG7679
Source for merge of: Vha100-2 BcDNA:LD21735
Source for merge of: Vha100-2 anon-WO0118547.296
"Vha100-2" may correspond to "Scim33". Sequence analysis off ends of P{SUPor-P} in Scim insertion mutant places "Scim33" near/in "Vha100-2" or "CG7682".
Source for merge of Vha100-2 anon-WO0118547.296 was sequence comparison ( date:051113 ).
"sprd" may correspond to "CG44009" or "Vha100-2" or both; the P{PZ}sprd05284 insertion maps within "CG44009" and "Vha100-2".
Source for identity of: BcDNA:LD21735 CG7679