Aberration Dmel\Df(3L)h-i22
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(3L)h-i22 | Species | D. melanogaster |
| Name | FlyBase ID | FBab0002374 | |
| Feature type | chromosomal_deletion | Created / Updated | 2006-08-22/2006-08-22 |
| Formalized genetic data | bk1 << h << dally hits bk2 << l(3)s2383 | ||
| Sequence coordinates | |||
| Deleted segment | 66D10--66E2 | ||
| Duplicated segment | |||
| Computed Breakpoints include | 66D10;66E1-66E2 | ||
| Breakpoints Inherited | |||
Nature of the Aberration
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| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 66D9;66E1 66D10;66D14 66D10-66D11;66E1-66E2 66D10;66E1-66E2 | ||
| 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 polytene analysis (FBrf0072831) Right limit of break 1 from inclusion of h (FBrf0042642) Left limit of break 2 from inclusion of dally (FBrf0110960) Right limit of break 2 from non-inclusion of dally (FBrf0110960) Ref: FBrf0042642. | |||
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 | |||
| Partially 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 | Deficient embryos show an uninterpretable mutant midgut phenotype. 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. Heterozygosity for Df(3L)h-i22 results in 0.0% 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. Heterozygotes with Df(3L)tra display a genitalia defective phenotype, all or parts of the genital disc derivatives are missing. No second site non-complementing phenotype with zipEbr and zipmhc-c6.1. Poor ventral cord organisation. Shows no maternal enhancement of dpphr4. Tracheal patterning and lumen size is disrupted in Df(3L)h-i22 embryos. homozygous lethal | ||
Position Effect Variegation Data
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Stocks
( 2 ) | |||
| Bloomington | |||
| Kyoto | |||
Notes on Origin
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| Discoverer | Belote. | ||
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
( 10 ) | |||
| Reported As | |||
| Symbol Synonym | Df(3L)h,i22 Df(3L)h122 Df(3L)hi22 Df(3L)hi22 Df(3L)h-i22 Df(3L)h-i22ry506 hi22 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
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References
( 59 ) | |||
| Generate a list of | |||
| List References by type |
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Recent research papers ( 2 ) | |||
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Nature of the Aberration