FB2024_03 , released June 25, 2024
Aberration: Dmel\Dp(1;Y)y261l
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General Information
Symbol
Dp(1;Y)y261l
Species
D. melanogaster
Name
FlyBase ID
FBab0003239
Feature type
interchromosomal_duplication
Also Known As
y2Y61l
Computed Breakpoints include

h1-h25B;1B14

Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
X ray
Class of aberration (relative to wild type)
interchromosomal_duplication
Class of aberration (relative to progenitor)
chromosomal_deletion
Breakpoints

h1-h25B;1B14

(Craymer and Roy, 1980)

[];1B14

(White et al., 1983)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data
Genetic mapping information
Comments
Comments on Cytology

All limits from polytene analysis (FBrf0034402)

Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
Partially deleted / disrupted
Molecular Data
Completely deleted
Partially deleted
Genes NOT Deleted / Disrupted
Complementation Data
 
Molecular Data
 
Genes Duplicated
Complementation Data
Completely duplicated
elav
(White et al., 1983)
l(1)1Bl
(White et al., 1983)
vnd
(Jimenez and Campos-Ortega, 1990, White et al., 1983)
y
(Woodard et al., 1989)
Partially duplicated
Molecular Data
Completely duplicated
Partially duplicated
Genes NOT Duplicated
Complementation Data
 
ota2
(Woodard et al., 1989)
ota7
(Woodard et al., 1989)
Molecular Data
 
Phenotypic Data
In combination with other aberrations

Df(1)BSC843 is rescued by Dp(1;Y)y261l.

(Christensen et al., 2009.7.21)

Inferred to overlap with: Df(1)BSC843.

(Christensen et al., 2009.7.21)
NOT in combination with other aberrations

Two copies of the duplication produces neural hyperplasic defects, characteristic of weak neurogenic mutants, of variable extent in the ventral cord.

(Jimenez and Campos-Ortega, 1990)
Stocks (7)
Notes on Origin
Discoverer

Lefevre.

 

Derived from XYL.YL, y2 su(wa) wa chromosome (origin obscure). deletion of majority of euchromatin

Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (6)
References (10)