FB2024_03 , released June 25, 2024
Allele: Dmel\H20
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General Information
Symbol
Dmel\H20
Species
D. melanogaster
Name
FlyBase ID
FBal0005311
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Mutagen
Nature of the Allele
Progenitor genotype
Cytology

Polytene chromosomes normal.

Description

Inversion of a 2kb fragment with both breakpoints within the H coding region.

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 bristle loss phenotype of H20/HE31 can be suppressed by deleting components of the E(spl)-complex. The degree of suppression depends on both the number and identity of E(spl)-complex transcription units removed. Rescued bristles display a double socket phenotype. Clonal analysis revealed that the gro mutant bristle tufting phenotype is epistatic to the H null bristle loss phenotype.

Bristle loss on head and notum and double socket phenotype.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Suppressor of
Statement
Reference

H20 is a suppressor of phenotype of Brdunspecified

Additional Comments
Genetic Interactions
Statement
Reference

Dominant suppressor of Brd: due to haploinsufficiency.

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

Posakony/Groger.

Comments
Comments

Strong H allele.

Phenotypic series of H alleles correlates with severity of molecular defects: in order of decreasing severity H18 = H20 > H21 > HD179.

H20/HE31 is used as the standard null genotype.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (4)