Aberration Dmel\Df(2R)cn83c
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(2R)cn83c | Species | D. melanogaster |
| Name | Deficiency (2R) cinnabar | FlyBase ID | FBab0002120 |
| Feature type | chromosomal_deletion | Created / Updated | 2006-08-22/2006-08-22 |
| Formalized genetic data | bk1 << dpld << sax << bk2 | ||
| Sequence coordinates | |||
| Deleted segment | 43C5--44C1 | ||
| Duplicated segment | |||
| Computed Breakpoints include | 43C5;44B6-44C1 | ||
| Breakpoints Inherited | |||
Nature of the Aberration
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| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 43C5;44B6-44C1 43C5-43D1;44B6-44C1 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Genetic mapping information | |||
| Comments | |||
Comments on Cytology
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All limits from polytene analysis (FBrf0074016) | |||
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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Phenotypic Data
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| In combination with other aberrations | |||
| NOT in combination with other aberrations | Dominantly causes tergite defects in less than 50% of run3 heterozygotes. Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2. Homozygous embryos have smaller heads than normal, and have abnormal tracheae and segmentation. The midgut is smaller than normal, does not constrict and the midgut primordia do not fuse in some embryos. The hindgut and Malpighian tubules are variable in length and crinkled. Large ventral cord cells. | ||
Position Effect Variegation Data
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Stocks
( 2 ) | |||
| Bloomington | 3136 | ||
| Kyoto | 106873 | ||
Notes on Origin
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| Discoverer | |||
Recovered as apparent cn double recombinants from test crosses of dysgenic-type males that were heterozygous for a maternally derived dp b cn bw second chromosome and paternally derived autosomes extracted from natural populations and capable of promoting male recombination. | |||
Balancer / Genotype Variants of the Aberration
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Separable Components
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Other Comments
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The Df(2R)cn83c chromosome may 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), but the eye colour phenotype in the presence of Df(2R)cn83c overlaps the eye colour phenotype in a wild-type background so it cannot be unequivocally demonstrated that the deficiency chromosome uncovers a suppressor of telomeric silencing. In addition, any suppression is a false positive result (the suppressor is not within the bounds of the deficient region) because the region of the deficiency is covered by one or more nonsuppressing deficiencies. | |||
Synonyms & Secondary IDs
( 3 ) | |||
| Reported As | |||
| Symbol Synonym | Df3136 Df(2R)cn83c | ||
| Name Synonym | Deficiency (2R) cinnabar | ||
| Secondary FlyBase IDs | |||
References
( 14 ) | |||
| Research paper |
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| Personal communication to FlyBase |
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| FlyBase analysis |
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| Book |
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Nature of the Aberration