A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\Fmr1I307N.Scer\UAS

General Information
SymbolDmel\Fmr1I307N.Scer\UASSpeciesD. melanogaster
NameFlyBase IDFBal0120822
Feature typealleleAssociated geneDmel\Fmr1
Allele class
Mutagenin vitro construct - amino acid replacement
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Description
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FB2013_03
FB2013_02
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Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
Additional Notes
References
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
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Progenitor genotype
Nature of the lesion
Statement
Reference
Construct: Amino acid replacement: I307N.
Carried in construct
Cytology
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dorsal cluster neuron & neurite, with Scer\GAL4ato.3.6
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Statement
Reference
Phenotype similar to but less severe than that in loss of function mutants. Only occasionally do fibers cross from the lobula to the medulla, but those that do form aberrant projection and branching patterns within the medulla. Effect is the same whether in a wild type or a Fmr1Δ113M/Fmr1Δ83M background.
Expression of Fmr1I307N.Scer\UAS in the eye driven by Scer\GAL4hs.2sev produces a mild eye phenotype. Overexpression also leads to the alteration of rhabdomere shape.
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hide Synonyms & Secondary IDs ( 1 )
Reported As
Symbol Synonym
Fmr1I307N.Scer\UAS
 
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Secondary FlyBase IDs
hide References ( 2 )
Research paper
Morales et al., 2002, Neuron 34(6): 961--972
Drosophila Fragile X protein, DFXR, regulates neuronal morphology and function in the brain. [FBrf0149142]
Wan et al., 2000, Mol. Cell. Biol. 20(22): 8536--8547
Characterization of dFMR1, a Drosophila melanogaster Homolog of the Fragile X Mental Retardation Protein. [FBrf0130150]