Aberration Dmel\Df(3R)red1
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(3R)red1 | Species | D. melanogaster |
| Name | Deficiency (3R) red Malpighian tubules | FlyBase ID | FBab0002877 |
| Feature type | chromosomal_deletion | ||
| Also Known As | Df(3R)red1 | ||
| Computed Breakpoints include | [<88A2];88C1--D1 | ||
| Deleted segment | 88A2--88D1 | ||
| Sequence coordinates | |||
| Member of large scale dataset(s) | |||
Recent Updates
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| Description |
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| FB2013_03 | |||
| FB2013_02 | |||
| All updates | Click here to see a list of all updates to this record from FB2010_08 and on. | ||
Nature of the Aberration
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| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 88B1;88D2-88D3 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Formalized genetic data | bk1 << cash << bk2 << put | ||
| Genetic mapping information | |||
| Comments | |||
Comments on Cytology
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Right limit of break 1 from inclusion of ems (FBrf0049810) Left limit of break 2 from inclusion of l(3)06951 (FBrf0067338) Right limit of break 2 from non-inclusion of l(3)03719 (FBrf0067338) | |||
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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Phenotypic Data
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| In combination with other aberrations | |||
| NOT in combination with other aberrations | Homozygotes for Df(3R)red1 fail to hatch. The Df(3R)red1 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). Heterozygosity for Df(3R)red1 results in 1.6% X chromosome nondisjunction and 0.6% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females. Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome. Dominantly causes tergite defects in less than 50% of run3 heterozygotes. Midgut development of mutant embryos is wild type. Heterozygosity for this deletion enhances the mutant ovarian phenotype of ovoD2. Df(3R)red/+ progeny of Df(1)C128/+ females show a high frequency of homeotic transformations (Gans et al., 1980). | ||
Stocks
( 2 ) | |||
| Bloomington | 3341 | ||
| Kyoto | 106989 | ||
Notes on Origin
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| Discoverer | |||
Balancer / Genotype Variants of the Aberration
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Separable Components
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Other Comments
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Synonyms & Secondary IDs
( 4 ) | |||
| Reported As | |||
| Symbol Synonym | Df(3R)red Df(3R)red1 Df(3R)red1 | ||
| Name Synonym | Deficiency (3R) red Malpighian tubules | ||
| Secondary FlyBase IDs | |||
References
( 28 ) | |||
| Generate a list of | |||
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Recent research papers (0)
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| All research papers listed in FlyBase were published before 2011 | |||
Recent Updates