FB2024_03 , released June 25, 2024
Allele: Dmel\SxlfP7A1
Open Close
General Information
Symbol
Dmel\SxlfP7A1
Species
D. melanogaster
Name
FlyBase ID
FBal0016692
Feature type
allele
Associated gene
Dmel\Sxl
Associated Insertion(s)
P{?'}SxlfP7A1
Carried in Construct
Key Links
Allele class

hypomorphic allele - genetic evidence

Mutagen
Nature of the Allele
Allele class

hypomorphic allele - genetic evidence

(Lindsley and Zimm, 1992)
Mutagen
PM hybrid dysgenesis
(Lindsley and Zimm, 1992, Salz et al., 1987)
Progenitor genotype
SxlfPb
(Lindsley and Zimm, 1992, Salz et al., 1987)
Associated Insertion(s)
P{?'}SxlfP7A1
Cytology
Description

Intragenic deletion within SxlfPb.

(Lindsley and Zimm, 1992)

Deletion of sequences from 0 to -6.5 (coordinates according to FBrf0042036). The distal AvaII site of the P-element present in the progenitor is missing, suggesting that the deletion extends into the distal P-element terminal repeat.

(Salz et al., 1987)
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 ( 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

      Fails to complement Sxl alleles that are defective in somatic function, suggesting that this allele probably eliminates all known somatic functions. Partially complements Sxlf2, an allele defective in germline function; heteroallelic females are semi-fertile and the ovaries do not contain any abnormal oocytes.

      (Salz et al., 1987)
      External Data
      Interactions
      Show genetic interaction network for Enhancers & Suppressors
      Phenotypic Class
      Phenotype Manifest In
      Additional Comments
      Genetic Interactions
      Statement
      Reference
      Xenogenetic Interactions
      Statement
      Reference
      Complementation and Rescue Data
      Comments
      Images (0)
      Mutant
      Wild-type
      Stocks (0)
      Notes on Origin
      Discoverer
      Comments
      Comments

      Isolated on the basis of its failure to complement Sxlf9.

      (Salz et al., 1987)
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (3)
      Reported As
      Symbol Synonym
      Sxlf7A1
      (Lindsley and Zimm, 1992, Oliver et al., 1990)
      Sxlf7AI
      (Salz et al., 1987)
      SxlfP7A1
      Name Synonyms
      Secondary FlyBase IDs
        References (4)