FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\E(spl)m8-HLHrv1
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General Information
Symbol
Dmel\E(spl)m8-HLHrv1
Species
D. melanogaster
Name
FlyBase ID
FBal0028166
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
E(spl)R1, E(spl)rv1
Key Links
Allele class
Mutagen
Nature of the Allele
Allele class
Mutagen
Caused by aberration
Cytology
Description

Large deletion.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
Expression Data
Reporter Expression
Additional Information
Statement
Reference
 
Marker for
Reflects expression of
Reporter construct used in assay
Human Disease Associations
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 0 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 0 )
Disease
Interaction
References
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

The number of corpora cardiaca cells is increased in mutant stage 17 embryos compared to wild type.

Additional neuroblasts are found in each position where the S1 neuroblasts normally form in mutant embryos.

The number of cells in the nau-expressing muscle precursor clusters is increased compared to wild-type in homozygous embryos and in homozygous embryos derived from homozygous female germline clones (lacking both maternal and zygotic function).

E(spl)rv1 shows severe neural hypertrophy, a 6--9 fold increase in nau expressing cells per cluster relative to wild type. The clusters enlarge so much that they merge to form superclusters across the midline.

Extreme embryonic neurogenic phenotype. Only remaining epidermis is indicated by a patch of cuticle in which a posterior spiracle and the remains of the pharynx are evident.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhancer of
Statement
Reference

E(spl)m8-HLHrv1/E(spl)m8-HLH[+] is an enhancer of visible phenotype of Scer\GAL4Tub.PU, cswN308D.UASp

Suppressor of
Statement
Reference
Phenotype Manifest In
Enhancer of
Statement
Reference

E(spl)m8-HLHrv1/E(spl)m8-HLH[+] is an enhancer of wing vein | ectopic phenotype of Scer\GAL4Tub.PU, cswN308D.UASp

Additional Comments
Genetic Interactions
Statement
Reference

E(spl)rv1 SoxNGA1192 double mutant embryos show a combination of the neurogenic E(spl)rv1 phenotype and the anti-neural SoxNGA1192 phenotype. The neurogenic phenotype is apparent in the ventral column of the S1 neuroblasts. In the lateral column, the anti-neural phenotype of SoxNGA1192 remains unchanged in the double mutant embryos.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer

Revertant.

Comments
Comments

Identification: Isolated by X-ray mutagenesis of E(spl)1 followed by screening for loss of ability to enhance Nspl-1.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (5)
References (18)