Aberration Dmel\Df(3R)awd-KRB
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(3R)awd-KRB | Species | D. melanogaster |
| Name | FlyBase ID | FBab0000009 | |
| Feature type | chromosomal_deletion | Created / Updated | 2006-08-22/2006-08-22 |
| Formalized genetic data | Med << bk1 << l(3)100CDa << bk2 | ||
| Sequence coordinates | |||
| Deleted segment | 100D1--100D4 | ||
| Duplicated segment | |||
| Computed Breakpoints include | 100D1;100D3-100D4 | ||
| Breakpoints Inherited | |||
Nature of the Aberration
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| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 100C;100D 100C6-100D1;100D1-100D4 100C6-100C7;100D3-100D4 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Genetic mapping information | |||
| Comments | Breakpoint(s) molecularly mapped | ||
Comments on Cytology
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Left limit of break 1 from non-inclusion of Med (FBrf0086254) Right limit of break 1 from polytene analysis (FBrf0086254) Left limit of break 2 from polytene analysis (FBrf0102610) Right limit of break 2 from polytene analysis (FBrf0086254) Ref: FBrf0048096. | |||
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 | Df(3R)awd-KRB homozygous embryos exhibit major disruption of the tracheal network accompanied by ectopic branching and looping, appearance of a few extra branches or "knobs", and migration abnormalities. Deficient embryos show an uninterpretable mutant midgut phenotype. Does not give a Minute phenotype when heterozygous. Dominantly causes tergite defects in less than 50% of run3 heterozygotes. Has a partially penetrant dominant cuticle phenotype. Heterozygous embryos sometimes have gaps (consisting of patches of naked cuticle) in the denticle belts. Homozygous embryos are very abnormal compared to wild-type. No second site non-complementing phenotype with zipEbr and zipmhc-c6.1. Shows no maternal enhancement of dpphr4. The Df(3R)awd-KRB 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
( 2 ) | |||
| Bloomington | |||
| Kyoto | |||
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
( 5 ) | |||
| Reported As | |||
| Symbol Synonym | Df(3R)awd Df(3R)awdKRB Df(3R)awdkrb Df(3R)awd-KRB Df(3R)KRB | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 35 ) | |||
| Generate a list of | |||
| List References by type |
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Recent research papers ( 1 ) | |||
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Nature of the Aberration