FB2025_01 , released February 20, 2025
Allele: Dmel\Pur1
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General Information
Symbol
Dmel\Pur1
Species
D. melanogaster
Name
recessive
FlyBase ID
FBal0014013
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Mutagen
Nature of the Allele
Allele class
Progenitor genotype
Caused by aberration
Cytology
Description

roo insertion in the eye specific region.

Mutation spans the head specific region and the distal lethal region.

GTP cyclohydrolase activity is severely reduced in the adult head, nearly normal in the adult body and moderately reduced in the prepupa of homozygotes.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
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 ( 1 )
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

Pur1 heterozygotes do not exhibit a eye degeneration phenotype.

Slight transient dilution of eye color in freshly emerged heterozygotes.

Recessive eye colour phenotype.

Eye colour: white to pale-orange. Severely reduced pteridine levels in the head.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Enhancer of
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

A Pur1, heterozygous background enhances the Scer\GAL4GMR.PF-> Ube3aCA.Scer\UAS.T:Zzzz\FLAG rough eye phenotype, causing a glazed appearance, loss of inter-ommatidial bristles and a yellowish discoloration, indicative of underlying neurodegeneration.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (2)
Stocks (1)
Notes on Origin
Discoverer
Comments
Comments

The viability and eye phenotype in trans with other Pu alleles has been determined.

Class I allele: eye specific phenotypes.

ry protein levels are less than normal in the eyes of this mutant.

GTP CH activity moderately reduced in prepupae and nearly normal in adult bodies of homozygotes; activity appears to be virtually absent in adult heads.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Name Synonyms
recessive
Secondary FlyBase IDs
    References (13)