FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\PginNC1
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General Information
Symbol
Dmel\PginNC1
Species
D. melanogaster
Name
FlyBase ID
FBal0048898
Feature type
allele
Associated gene
Dmel\Pgi
Associated Insertion(s)
Carried in Construct
Key Links
Allele class

loss of function allele

Mutagen
Nature of the Allele
Allele class

loss of function allele

(Burkhart et al., 1984)
Mutagen
natural population
(Burkhart et al., 1984)
Progenitor genotype
Cytology
Description
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Variant Molecular Consequences
Associated Sequence Data
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
 
UniProtKB/Swiss-Prot
    UniProtKB/TrEMBL
      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
      exacerbates  Huntington's disease
      modeled by Hsap\HTT128Q.1-336.UAS
      (Kaltenbach et al., 2007)
      Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
       
      Disease-implicated variant(s)
       
      Phenotypic Data
      Phenotypic Class
      Phenotype Manifest In
      Detailed Description
      Statement
      Reference

      Phenotypic category: Pgi-

      (Lindsley and Zimm, 1992)
      External Data
      Interactions
      Show genetic interaction network for Enhancers & Suppressors
      Phenotypic Class
      Enhancer of
      Statement
      Reference

      PginNC1 is an enhancer of visible phenotype of Hsap\HTT128Q.1-336.UAS, Scer\GAL4GMR.PU

      (Kaltenbach et al., 2007)
      Phenotype Manifest In
      Enhancer of
      Statement
      Reference

      PginNC1 is an enhancer of eye phenotype of Hsap\HTT128Q.1-336.UAS, Scer\GAL4GMR.PU

      (Kaltenbach et al., 2007)
      Additional Comments
      Genetic Interactions
      Statement
      Reference
      Xenogenetic Interactions
      Statement
      Reference
      Complementation and Rescue Data
      Comments

      Out of a total of 716 alleles collected in North Carolina, one null allele was recovered.

      (Langley et al., 1981)
      Images (0)
      Mutant
      Wild-type
      Stocks (2)
      Notes on Origin
      Discoverer

      Isolated from: Raleigh, North Carolina population, June 1977.

      (Burkhart et al., 1984)
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (6)
      Reported As
      Symbol Synonym
      PgiNC1
      (Lindsley and Zimm, 1992)
      Pgin1
      (Lindsley and Zimm, 1992)
      PginNC1
      PginNC80
      (Lindsley and Zimm, 1992)
      PginNc80
      (Lindsley and Zimm, 1992)
      nNC1
      (Kaltenbach et al., 2007)
      Name Synonyms
      Secondary FlyBase IDs
      • FBal0013700
      References (5)