FB2022_02, released March 29, 2022

Aberration: Dmel\Df(3L)fz-M21

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General Information
Symbol
Df(3L)fz-M21
Species
D. melanogaster
Name
FlyBase ID
FBab0002373
Feature type
chromosomal_deletion
Also Known As
Df(3L)fzM21
Computed Breakpoints include

70D2;71E4-71E5

Features within 70D2--71E5
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
gamma ray
(Smyth and Belote, 1999)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Smyth and Belote, 1999, Clark and McKearin, 1996, Coyne, 1996, Nambu and Nambu, 1996, Tear et al., 1996, Pauli et al., 1995, Carpenter, 1994, Landecker et al., 1994)
Breakpoints

70D2;71E

(Carpenter, 1994)

70D2-70D3;71E4-71E5

(Coyne, 1996, Nambu and Nambu, 1996, Tear et al., 1996, Pauli et al., 1995, Landecker et al., 1994)

70D2-70D3;70E4-70E5

(Clark and McKearin, 1996)

70D3;71E5

(Smyth and Belote, 1999)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

btl << bk1 << fz << gnu << bk2

Genetic mapping information
Comments

This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).

(Marygold et al., 2007)
Comments on Cytology

Limits of break 1 from polytene analysis (FBrf0075380) Limits of break 2 from polytene analysis (FBrf0076124)

Sequence Crossreferences
DDBJ / EMBL / GenBank
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
 
Affected Genes Inferred by Location
    Phenotypic Data
    In combination with other aberrations
    NOT in combination with other aberrations

    Flies heterozygous for the deletion do not show a Minute bristle phenotype.

    (Marygold et al., 2007)

    Df(3L)fz-M21 embryos show defects in tracheal cell migration.

    (Myat et al., 2005)

    The Df(3L)fz-M21 chromosome does not act as a dominant suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion).

    (Mason et al., 2004)

    Shows dominant enhancement of dominant haltere phenotype caused by Ubx195 and Ubx9.22.

    (Burnette et al., 1999)

    Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.

    (Coyne et al., 1998)

    No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.

    (Halsell and Kiehart, 1998)

    Deficient embryos show an uninterpretable mutant midgut phenotype.

    (Bilder and Scott, 1995)

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

    (Pauli et al., 1995)

    Trl hemizygous adult males show strong homeotic transformation of the sixth sternite into the fifth as shown by the presence of a bristles on the sixth sternite.

    (Farkas et al., 1994)
    Stocks (5)
    Notes on Origin
    Discoverer

    Adler.

     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     

    Used in D.melanogaster/D.simulans hybrids to map at least four non-overlapping regions on the D.simulans 3R that have effects on the species difference of cuticular hydrocarbon profile.

    (Coyne, 1996)

    "70D2;71E" was stated as revision.

    (Carpenter, 1994)
    Synonyms and Secondary IDs (7)
    References (55)