Aberration Dmel\Df(3L)rdgC-co2
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(3L)rdgC-co2 | Species | D. melanogaster |
| Name | FlyBase ID | FBab0002392 | |
| Feature type | chromosomal_deletion | Created / Updated | 2006-08-22/2006-08-22 |
| Formalized genetic data | Su(Tpl) << bk1 << polo << fbl << bk2 << l(3)j7C3 | ||
| Sequence coordinates | |||
| Deleted segment | 77A1--77D1 | ||
| Duplicated segment | |||
| Computed Breakpoints include | 77A1;77D1 | ||
| Breakpoints Inherited | |||
Nature of the Aberration
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| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 77A1;77D | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Genetic mapping information | |||
| Comments | |||
Comments on Cytology
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All limits from polytene analysis (FBrf0064394) Previously reported to delete cp, however this was due to Df(3L)rdgC-co2 chromosome carrying cp[1]. cp[1] is separable from Df(3L)rdgC-co2 by recombination. | |||
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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FlyBase curator comment: FBrf0123112 reported that Df(3L)rdgC-co2 deletes cp, however Kennison, 2006.7.21, personal communication to FlyBase, showed that Df(3L)rdgC-co2 is not deleted for cp, but in fact carries cp1. | |||
Phenotypic Data
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| In combination with other aberrations | |||
| NOT in combination with other aberrations | Deficient embryos show an uninterpretable mutant midgut phenotype. Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome. Heterozygosity for Df(3L)rdgC-co2 results in 2.3% X chromosome nondisjunction and 3.4% 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. Homozygous mutants embryos show a failure to form a ventral furrow. The mesoderm primordium is internalised late. Shows no maternal enhancement of dpphr4. The Df(3L)rdgC-co2 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). Weak second site non-complementing phenotype with zipEbr and zipmhc-c6.1: malformed phenotype penetrance 10-24%. | ||
Position Effect Variegation Data
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Stocks
( 3 ) | |||
| Kyoto | |||
| Bloomington | |||
Notes on Origin
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| Discoverer | |||
Induced on: marked third chromosome that carried the cp[1] allele. | |||
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
( 9 ) | |||
| Reported As | |||
| Symbol Synonym | Df(3L)rdgC Df(3L)rdgCco2 Df(3L)rdgC-cd Df(3L)rdgC-Ci2 Df(3L)rdgC-co Df(3L)rdgC-co2 Df(3L)rdgc-cos2 rdgC rdgC-co2 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 51 ) | |||
| Generate a list of | |||
| List References by type |
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Recent research papers ( 3 ) | |||
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Nature of the Aberration