Aberration Dmel\Df(3L)fz-D21
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(3L)fz-D21 | Species | D. melanogaster |
| Name | FlyBase ID | FBab0002370 | |
| Feature type | chromosomal_deletion | Created / Updated | 2006-08-22/2006-08-22 |
| Formalized genetic data | Hsc70Cb << bk1 << D << shd << bk2 << gnu | ||
| Sequence coordinates | |||
| Deleted segment | 70D2--70E8 | ||
| Duplicated segment | |||
| Computed Breakpoints include | 70D2;70E8 | ||
| Breakpoints Inherited | |||
Nature of the Aberration
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| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 70D2;70E8 70D3;70E3-70E8 70D;71F 70D1-70D2;70E7 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Genetic mapping information | |||
| Comments | |||
Comments on Cytology
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Left limit of break 1 from polytene analysis (FBrf0075380) Right limit of break 1 from inclusion of D (FBrf0075380) Limits of break 2 from polytene analysis (FBrf0075380) | |||
Molecularly Mapped Breakpoints
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Sequence Crossreferences
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| DDBJ
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EMBL / GenBank | DNA sequence Protein sequence Name | ||
Gene Deletion & Duplication Data
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Genes Deleted / Disrupted
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| Complementation Data | |||
| Completely deleted / disrupted | |||
| Molecular Data | |||
Genes NOT Deleted / Disrupted
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| Complementation Data | |||
| Molecular Data | |||
Genes Duplicated
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| Complementation Data | |||
| Molecular Data | |||
Genes NOT Duplicated
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| Complementation Data | |||
| Molecular Data | |||
Related Comments
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Does not delete P{lacW}endosS067006 | |||
Phenotypic Data
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| In combination with other aberrations | |||
| NOT in combination with other aberrations | Double mutants of fz21, fz23 or Df(3L)fz-D21 with Df(3L)fz2 show variable embryonic segmentation defects ranging from a few extra denticles in the posterior part of some segments to complete replacement of naked cuticle with denticles. This phenotype is reminiscent of that for P{en1}wgen11 loss of function. Exhibit dominant suppression of Pc. Heterozygosity for Df(3L)fz-D21 results in 1.1% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females. Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2. No effect on the eye pigment phenotype of wT81. Shows no maternal enhancement of dpphr4. The Df(3L)fz-D21 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). | ||
Position Effect Variegation Data
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Stocks
( 3 ) | |||
| Bloomington | |||
| Kyoto | |||
Notes on Origin
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| Discoverer | Adler. | ||
Balancer / Genotype Variants of the Aberration
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Separable Components
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Other Comments
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"70D2;70E8" was stated as revision. | |||
Synonyms & Secondary IDs
( 7 ) | |||
| Reported As | |||
| Symbol Synonym | Df(3L)fzD21 Df(3L)fz D21 Df(3L)fzD21 Df(3L)fz-d21 Df(3L)fz-D21 fzD21 fzD21 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
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References
( 47 ) | |||
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Recent research papers ( 1 ) | |||
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Nature of the Aberration