FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Aberration: Dmel\In(3R)H88d
Open Close
General Information
Symbol
In(3R)H88d
Species
D. melanogaster
Name
FlyBase ID
FBab0022920
Feature type
chromosomal_inversion
Computed Breakpoints include

92E14;93A1-93A2

Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
ethyl methanesulfonate
(Maier et al., 1992)
Class of aberration (relative to wild type)
chromosomal_inversion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_inversion
(Maier et al., 1992)
Breakpoints

92E12-92E15;93A1-93A2

(Maier et al., 1992)
Causes alleles
H88d
(Maier et al., 1992)
Carries alleles
Transposon Insertions
Formalized genetic data

bk1 hits H << bk2

Genetic mapping information
Comments
Comments on Cytology

Limits of break 1 from complementation mapping against H (FBrf0057132) Limits of break 2 from polytene analysis (FBrf0057132)

Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
H
(Maier et al., 1992)
Partially deleted / disrupted
Molecular Data
Completely deleted
Partially deleted
Genes NOT Deleted / Disrupted
Complementation Data
 
Molecular Data
 
Genes Duplicated
Complementation Data
Completely duplicated
Partially duplicated
Molecular Data
Completely duplicated
Partially duplicated
Genes NOT Duplicated
Complementation Data
 
Molecular Data
 
Affected Genes Inferred by Location (0)
    If no genes are listed here, it may be because the affected region is very large. The JBrowse insert above may show an error for the same reason, and other FlyBase tools such as CytoSearch may also fail for large regions. You can contact FlyBase for more help.
    In these cases, there will be no "Export to Hitlist" button to the left.
    Phenotypic Data
    In combination with other aberrations

    In(3R)H88d/TM6B shows extreme venation defects in L2 and the posterior crossvein is disrupted, with L5 complete.

    (Maier et al., 1992)
    NOT in combination with other aberrations

    Intermediate H phenotype, and is recessive lethal. Possibly carries a deletion starting in H transcription unit.

    (Maier et al., 1992)
    Stocks (0)
    Notes on Origin
    Discoverer

    W. Welshons.

    (Maier et al., 1992)
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (1)
    Reported As
    Symbol Synonym
    In(3R)H88d
    Name Synonyms
    Secondary FlyBase IDs
      References (2)