Aberration Dmel\Df(2L)30A-C
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(2L)30A-C | Species | D. melanogaster |
| Name | FlyBase ID | FBab0001390 | |
| Feature type | chromosomal_deletion | Created / Updated | 2006-08-22/2006-08-22 |
| Formalized genetic data | raw << bk1 << Cks30A << l(2)DA2 << bk2 << ms(2)30C | ||
| Sequence coordinates | |||
| Deleted segment | 30A3--30C5 | ||
| Duplicated segment | |||
| Computed Breakpoints include | 30A3-30A5;30C5 | ||
| Breakpoints Inherited | |||
Nature of the Aberration
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| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 30A3-30A6;30D3-30D4 29F7-30A1;30C2-30C5 29F7;30C5 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Genetic mapping information | |||
| Comments | |||
Comments on Cytology
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Left limit of break 1 from polytene analysis (FBrf0058516) Right limit of break 1 from inclusion of tai (FBrf0067338) Left limit of break 2 from polytene analysis (FBrf0093373) Right limit of break 2 from polytene analysis (FBrf0080145) Ref: Lindsley and Zimm, 1992 | |||
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 | 83% of hemisegments show an RP2 to RP2sib cell fate transformation in homozygous embryos. Deficient embryos show a mutant midgut phenotype: midgut primordia do not migrate from terminalia. Heterozygosity for Df(2L)30A-C results in 2.1% X chromosome nondisjunction and 2.5% 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. Intermediate second site non-complementing phenotype with zipEbr and zipmhc-c6.1: malformed phenotype penetrance 25-75%. Midgut primordia do not fuse, but remain at the anterior and posterior of the yolk mass in homozygous embryos. The hindgut is somewhat shorter than normal. The Malpighian tubules bud out but do not elongate. Shows a dose-sensitive interaction with pbhs.PB. Shows no maternal enhancement of dpphr4. The Df(2L)30A-C chromosome acts as a dominant weak 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 | 107181 | ||
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
( 6 ) | |||
| Reported As | |||
| Symbol Synonym | Df30A-C Df(2L)30A;C Df(2L)30A-C Df(2L)30C Df(2L)A-C Df(3L)30A-C | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 36 ) | |||
| Generate a list of | |||
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Recent research papers ( 1 ) | |||
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Nature of the Aberration