FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\cinπ1
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General Information
Symbol
Dmel\cinπ1
Species
D. melanogaster
Name
FlyBase ID
FBal0039206
Feature type
allele
Associated gene
Dmel\cin
Associated Insertion(s)
P{}cinπ1
Carried in Construct
Key Links
Genomic Maps

Allele class
Mutagen
Nature of the Allele
Allele class
Mutagen
PM hybrid dysgenesis
(Kamdar et al., 1994)
Progenitor genotype
Associated Insertion(s)
P{}cinπ1
Cytology
Description

The P{}cinπ1 insertion maps within a dicistronic processed transcript that encodes two non-overlapping open reading frames (cin and CG42376).

(FlyBase, 1996-)

400bp insertion.

(Kamdar et al., 1994)
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 ( 0 )
      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
      External Data
      Interactions
      Show genetic interaction network for Enhancers & Suppressors
      Phenotypic Class
      Suppressed by
      Statement
      Reference

      cinπ1 has female sterile phenotype, suppressible by Atha\cnx1hs.PW

      (Wittle et al., 1999)
      Other
      Statement
      Reference

      Atha\cnx1hs.PW, cinπ1 has female fertile phenotype

      (Wittle et al., 1999)
      Phenotype Manifest In
      Additional Comments
      Genetic Interactions
      Statement
      Reference
      Xenogenetic Interactions
      Statement
      Reference

      Aldehyde oxidase defect (indicative of MoCF defect) rescued by one copy of Atha\cnx1hs.PW, carried in P{hsp70-cnx1.W}.

      (Wittle et al., 1999)
      Complementation and Rescue Data
      Comments
      Images (0)
      Mutant
      Wild-type
      Stocks (0)
      Notes on Origin
      Discoverer
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (1)
      Reported As
      Symbol Synonym
      cinπ1
      Name Synonyms
      Secondary FlyBase IDs
        References (3)