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General Information
Symbol
Df(1)HA32
Species
D. melanogaster
Name
FlyBase ID
FBab0000413
Feature type
Computed Breakpoints include

6E4-6E5;7A6

Deleted Segment
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Class of aberration (relative to wild type)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

ogre << bk1 << l(1)6Ed << l(1)7Aa << bk2 << l(1)7Ab

Genetic mapping information
Comments

Breakpoint(s) molecularly mapped

Comments on Cytology

Deletion of 16/18 bands.

All limits from polytene analysis (FBrf0034402)

Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Genes NOT Deleted / Disrupted
Genes Duplicated
Complementation Data
Completely duplicated
Partially duplicated
Molecular Data
Completely duplicated
Partially duplicated
Genes NOT Duplicated
Complementation Data
 
Molecular Data
 
Phenotypic Data
In combination with other aberrations

Transmission rate of Dp(1;f)J21A through females to progeny is 28%, Df(1)HA32 has no effect on transmission.

NOT in combination with other aberrations

Shows no maternal enhancement of dpphr4.

Dominantly causes tergite defects in less than 50% of run3 heterozygotes.

Deficient embryos show an uninterpretable mutant midgut phenotype.

Homozygous embryos are very abnormal compared to wild-type.

Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.

No significant change in female lethality when in combination with Sxlf1.

Heterozygous females exhibit reduced viability and fertility.

Stocks (3)
Notes on Origin
Discoverer

Lefevre.

 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (3)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (35)