Aberration Dmel\Df(3L)W10
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(3L)W10 | Species | D. melanogaster |
| Name | Deficiency (3L) Wrinkled | FlyBase ID | FBab0002357 |
| Feature type | chromosomal_deletion | ||
| Also Known As | Df(3L)WR10, W10, Df(3L)Wr10 | ||
| Computed Breakpoints include | 75A6-75A7;75C2 | ||
| Deleted segment | 75A6--75C2 | ||
| Sequence coordinates | |||
| Member of large scale dataset(s) | |||
Recent Updates
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| Description |
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| FB2013_03 | |||
| FB2013_02 | |||
| All updates | Click here to see a list of all updates to this record from FB2010_08 and on. | ||
Nature of the Aberration
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| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 75A6-75A7;75C1-75C2 75A6-75A7;75C5-75C7 75A6-76A7;75C1-75C2 75A;75C1-75C2 75B3-75B6;75C 75B3-75B6;75C1-75C2 75B3;75C | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Formalized genetic data | bk1 << rhea << bk2 << not | ||
| Genetic mapping information | |||
| Comments | Breakpoint(s) molecularly mapped | ||
Comments on Cytology
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Left limit of break 1 from polytene analysis (FBrf0051843) Right limit of break 1 from polytene analysis (FBrf0082995) Left limit of break 2 from polytene analysis (citation unavailable) Right limit of break 2 from polytene analysis (FBrf0051843) | |||
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 enhances the KrIf-1/+ eye phenotype. Causes inviability or low viability in hybrid females when heterozygous with D.simulans chromosome. Intermediate second site non-complementing phenotype with zipEbr and zipmhc-c6.1: malformed phenotype penetrance 25-75%. Shows no maternal enhancement of dpphr4. Deficient embryos show a mutant midgut phenotype: posterior constriction forms anterior to normal site, anterior constriction fails to form. Homozygous embryos do not complete head involution and germband shortening, and tracheae are disrupted. Maintenance of the midgut epithelium, formation of midgut constrictions and elongation of the Malpighian tubules are variable. Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2. Number of cells expressing midline glial cell markers in the embryonic CNS is increased by 60%. Homozygotes show the full cell death defective phenotype. 75B puff is absent. | ||
Stocks
( 2 ) | |||
| Bloomington | |||
| Kyoto | |||
Notes on Origin
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| Discoverer | Segraves. | ||
Separable from: Cap-H2[TH1]. The Cap-H2[TH1] mutation was found on the Df(3L)W10 chromosome. | |||
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
( 13 ) | |||
| Reported As | |||
| Symbol Synonym | Df(3L)w10 Df(3L)W10 Df(3L)W+R Df(3L)Wr10 Df(3L)WR10 Df(3L)WR+10 Df(3L)Wrv Df(3L)WR10 Df(3L)W-R10 W+R10 WR10 | ||
| Name Synonym | Deficiency (3L) Wrinkled | ||
| Secondary FlyBase IDs | |||
References
( 48 ) | |||
| Generate a list of | |||
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Recent research papers (0)
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| All research papers listed in FlyBase were published before 2011 | |||
Recent reviews (0)
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| All reviews listed in FlyBase were published before 2011 | |||
Recent Updates