Aberration Dmel\Df(3R)sbd105
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(3R)sbd105 | Species | D. melanogaster |
| Name | Deficiency (3R) stubbloid | FlyBase ID | FBab0002921 |
| Feature type | chromosomal_deletion | ||
| Also Known As | Df(3R)sbd105, sbd105 | ||
| Computed Breakpoints include | 89A1;89B9-89B10 | ||
| Deleted segment | 89A1--89B10 | ||
| 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 | 88F9-89A1;89B4-89B5 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Formalized genetic data | l(3)neo44 << bk1 << mu1 << Sap47 << bk2 << gish | ||
| Genetic mapping information | |||
| Comments | Breakpoint(s) molecularly mapped Deletes entire Sb chromosome walk. Used as part of cloning strategy to jump from 88F into 89B. | ||
Comments on Cytology
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Left limit of break 1 from non-inclusion of l(3)neo44 (FBrf0067338) Right limit of break 1 from inclusion of spno (FBrf0056149) Left limit of break 2 from inclusion of Sb (FBrf0031288) Right limit of break 2 from polytene analysis (FBrf0031288) | |||
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 | Lethal with Df(3R)sbd45. Suppressor of In(1)wm4h position-effect variegation. | ||
| NOT in combination with other aberrations | Shows no maternal enhancement of dpphr4. Lethal as homozygote. Homozygous embryos are very abnormal compared to wild-type. Heterozygosity for this deletion enhances the mutant ovarian phenotype of ovoD2. Homozygous lethal. Crossing over in X reduced in Df(3R)sbd105/+ females (Hinton, 1966, Genetics 55: 157-64); no effect on spontaneous male recombination (Lutkin and Baker, 1979, Mutat. Res. 61: 221-27) | ||
Stocks
( 3 ) | |||
| 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
( 7 ) | |||
| Reported As | |||
| Symbol Synonym | Df(3R)sbd Df(3R)sbd-105 Df(3R)sbd105 Df(3R)sbd105 (Marenda et al., 2004, Fauvarque et al., 2001, Zhu et al., 2001, Hing et al., 1999, Crosby et al., 1999, Wustmann et al., 1989, Gonzalez-Reyes et al., 1997, Bernardoni et al., 1997, Sam et al., 1996, Andjelkovic et al., 1995, Awad et al., 1981, Heitzler et al., 1996, Burkhart et al., 1984, Gillespie and Berg, 1995, Becker et al., 1995, Wang et al., 1994, Reuter, 1994, Anderson and Nusslein-Volhard, 1984, Jurgens et al., 1984, Ramain et al., 1993, Nelson and Szauter, 1992, Webster et al., 1992, Hammonds and Fristrom, 2006, Yagi and Ip, 2005) Df-sbd105 | ||
| Name Synonym | Deficiency (3R) stubbloid | ||
| Secondary FlyBase IDs | |||
References
( 55 ) | |||
| 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 Updates