Allele Dmel\ro1
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\ro1 | Species | D. melanogaster |
| Name | FlyBase ID | FBal0014629 | |
| Feature type | allele | Created / Updated | 2006-05-15/2006-05-15 |
| Associated gene | Dmel\ro | ||
| Allele class | |||
| Mutagen | spontaneous | ||
Nature of the Allele
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| Allele class | |||
| Mutagen | |||
| Mapped Features and Mutations | |||
Type Symbol & Location Additional Notes References | |||
| Associated Sequence Data | |||
| DDBJ
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EMBL / GenBank | DNA sequence Protein sequence Name | ||
| UniProtKB/Swiss-Prot | |||
| UniProtKB/TrEMBL | |||
| Progenitor genotype | |||
| Nature of the lesion | Statement Reference Contains a >10 kb insertion homologous to 412 in intron 1 5' to homeobox (Tomlinson, Kimmel and Rubin, 1988). | ||
| Assay mode | |||
| Caused by insertion | |||
| Carried on aberration | |||
| Cytology | |||
Phenotypic Data
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Phenotypic Class
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Phenotype Manifest In
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Detailed Description
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Statement Reference 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. Disrupts an early stage of eye development: ommatidal array is disrupted, number of photoreceptors per ommatidia is variable. The ommatidial array is disrupted and the number of photoreceptor cells per ommatidium is variable. 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. Does not appear to have a gross defect on brain development. | |||
Interactions
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Phenotypic Class
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Enhancer of | |||
Statement Reference | |||
Phenotype Manifest In
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NOT Enhanced by | |||
Statement Reference | |||
Suppressed by | |||
Statement Reference | |||
Enhancer of | |||
Statement Reference | |||
Additional Comments
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Genetic Interactions
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Statement Reference Enhances the rough eye phenotype caused by expression of atoScer\UAS.cJa under the control of Scer\GAL4sca-109-68. | |||
Xenogenetic Interactions
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Statement Reference | |||
Complementation & Rescue Data
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| Rescued by | |||
| Comments | |||
Stocks
( 82 ) | |||
| Bloomington | 569 4064 496 | ||
| Kyoto | 105984 107569 105998 106007 | ||
Notes on Origin
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| Discoverer | Muller, June 1913. | ||
Comments
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No interaction with P{sev-svp1} or P{sev-svp2} exists. | |||
Synonyms & Secondary IDs
( 1 ) | |||
| Reported As | |||
| Symbol Synonym | ro1 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 17 ) | |||
| Research paper |
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| Book |
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Nature of the Allele