FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Ncc69PL00618
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General Information
Symbol
Dmel\Ncc69PL00618
Species
D. melanogaster
Name
FlyBase ID
FBal0161412
Feature type
allele
Associated gene
Dmel\Ncc69
Associated Insertion(s)
PBac{GAL4D,EYFP}Ncc69PL00618
Carried in Construct
Key Links
Genomic Maps

Allele class
Mutagen
Nature of the Allele
Allele class
Mutagen
P-element activity
(Gene Disruption Project members, 2001-)
Progenitor genotype
Associated Insertion(s)
PBac{GAL4D,EYFP}Ncc69PL00618
Cytology
Description
Allele components
Component
Use(s)
Inserted element
PBac{GAL4D,EYFP}
Encoded product / tool
GAL4(II-9)
Mutations Mapped to the Genome
Curation Data
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
      ameliorates  epilepsy
      modeled by kccDHS1
      (Hekmat-Scafe et al., 2010)
      Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
       
      Disease-implicated variant(s)
       
      Phenotypic Data
      Phenotypic Class
      Phenotype Manifest In
      Detailed Description
      Statement
      Reference
      External Data
      Interactions
      Show genetic interaction network for Enhancers & Suppressors
      Phenotypic Class
      Suppressor of
      Statement
      Reference

      Ncc69PL00618/Ncc69[+] is a suppressor of paralytic | recessive phenotype of kccDHS1

      (Hekmat-Scafe et al., 2010)
      Phenotype Manifest In
      Additional Comments
      Genetic Interactions
      Statement
      Reference

      The bang-sensitive paralytic phenotype of homozygous kccDHS1 mutants is only modestly suppressed by Ncc69PL00618/+.

      (Hekmat-Scafe et al., 2010)
      Xenogenetic Interactions
      Statement
      Reference
      Complementation and Rescue Data
      Comments
      Images (0)
      Mutant
      Wild-type
      Stocks (1)
      Notes on Origin
      Discoverer
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (2)
      Reported As
      Symbol Synonym
      CG4357PL00618
      Ncc69PL00618
      (Hekmat-Scafe et al., 2010)
      Name Synonyms
      Secondary FlyBase IDs
        References (2)