Aberration Dmel\Df(2L)net62
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(2L)net62 | Species | D. melanogaster |
| Name | FlyBase ID | FBab0001855 | |
| Feature type | chromosomal_deletion | ||
| Computed Breakpoints include | 21A1-21A4;21B4 | ||
| Deleted segment | 21A1--21B4 | ||
| Sequence coordinates | |||
Recent Updates
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| Description |
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| FB2012_01 | |||
| FB2011_10 | |||
| 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 | 21A;21B3-21B4 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Formalized genetic data | bk1 << l(2)gl << net << bk2 << al | ||
| Genetic mapping information | |||
| Comments | |||
Comments on Cytology
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Left limit of break 1 from polytene analysis (FBrf0031322) Right limit of break 1 from inclusion of l(2)gl (FBrf0031322) Left limit of break 2 from polytene analysis (citation unavailable) Right limit of break 2 from polytene analysis (FBrf0031322) | |||
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 | Heterozygotes have essentially normal wings, occasionally having a single extra vein near the posterior crossvein (12%). Homozygous lethal. Mutant phenotype rescued by P{l(2)gl-15}. Homozygous lethal. | ||
Stocks
( 2 ) | |||
| Bloomington | 3634 | ||
| Kyoto | 107143 | ||
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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The Df(2L)net62 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), but this is assumed to be a false positive result (the suppressor may not be within the bounds of the deficient region) because the 2L TAS array on the chromosome is missing or reduced (as assayed by in situ hybridization) and it has previously been shown (FBrf0137248, FBrf0158986) that partial or complete deficiency of the 2L TAS array on the homologue suppresses silencing of brown-red variants of P{3'WP-2,wvar}2Lt. In addition, the deficiency chromosome fails to complement lethal mutations of l(2)gl and deficiencies that are mutant for l(2)gl are often also deficient for the 2L TAS array (FBrf0137248). | |||
Synonyms & Secondary IDs
( 8 ) | |||
| Reported As | |||
| Symbol Synonym | Df(2)lgl net62 Df(2)net62 Df(2)net62 Df(2L)net Df(2L)net62 Df(2L)net62 l(2)gl net 62c net62 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 26 ) | |||
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Recent research papers (0)
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| All research papers listed in FlyBase were published before 2010 | |||
Recent Updates