FB2024_03 , released June 25, 2024
Allele: Dmel\ro1
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General Information
Symbol
Dmel\ro1
Species
D. melanogaster
Name
FlyBase ID
FBal0014629
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Mutagen
Nature of the Allele
Allele class
Progenitor genotype
Associated Insertion(s)
Cytology
Description

Contains a >10 kb insertion homologous to 412 in intron 1 5' to homeobox (Tomlinson, Kimmel and Rubin, 1988).

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Comment:

Site of a 21 bp insertion in the ro1 allele. There is also a 412 element insertion(412{}ro1) 85 bases further downstream in ro1.

Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
Expression Data
Reporter Expression
Additional Information
Statement
Reference
 
Marker for
Reflects expression of
Reporter construct used in assay
Human Disease Associations
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 0 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 0 )
Disease
Interaction
References
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

Does not appear to have a gross defect on brain development.

The R2/R5 precursor pair is transformed into R3/R4 in most preclusters in homozygous third larval instar eye discs. The overall arrangement and rotation of the clusters is abnormal, with some clusters rotating in the wrong direction and others not rotating. Mosaic ommatidia with mutant R3 and R4 cells behave like wild-type with respect to ommatidial polarity.

e4 wo1 ro1 mutant larvae show an abnormal response to UVC radiation.

The ommatidial array is disrupted and the number of photoreceptor cells per ommatidium is variable.

Disrupts an early stage of eye development: ommatidal array is disrupted, number of photoreceptors per ommatidia is variable.

Homozygotes have rough eyes; slightly smaller and narrower than wild type. Approximately normal numbers of facets but arrangement irregular; frequently have fewer and sometimes more than eight retinula cells; some facets missing such that three ommatidial bristles juxtaposed; other facets fused (Stemm-Tegethoff and Dicke, 1974; Ready, Hanson and Benzer, 1976). Fiber pathways through lamina and into medulla in considerable disarray; optic chiasma between the two replaced by parallel fibers; laminar cartridge and medullar columns deranged, ventral epithelial nuclear row absent; medulla displaced from normal position and rotated anteriorly. Mosaic studies demonstrate that phenotype is eye autonomous; i.e., the genotype of the eye dictates that of the underlying nervous elements.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhancer of
Statement
Reference
Phenotype Manifest In
NOT Enhanced by
Statement
Reference

ro1 has phenotype, non-enhanceable by astK6

Suppressed by
Statement
Reference

ro1 has phenotype, suppressible by Dfd::rotLa

Enhancer of
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

Enhances the rough eye phenotype caused by expression of atoScer\UAS.cJa under the control of Scer\GAL4sca-109-68.

The phenotype of ro1 homozygotes is not dominantly altered by astK6.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Comments
Images (1)
Stocks (74)
Notes on Origin
Discoverer

Muller, June 1913.

Comments
Comments

No interaction with P{sev-svp1} or P{sev-svp2} exists.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
ro1
Name Synonyms
Secondary FlyBase IDs
    References (17)