FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
Allele: Dmel\TfAP-2stummelbein
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General Information
Symbol
Dmel\TfAP-2stummelbein
Species
D. melanogaster
Name
stummelbein
FlyBase ID
FBal0123324
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
w#14.29
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Associated Insertion(s)
Cytology
Description

P{Mcp-w#14} insertion is located 87bp upstream of the first exon of the less extensive of the two splice variants of the AP-2 transcription unit, and thus is within the first intron of the more extensive of the two splice variants of the AP-2 transcription unit.

Mutations Mapped to the Genome
Curation Data
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 ( 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

Homozygotes are viable but have short legs. The joints of the legs are missing. The sex combs and transverse rows are correctly positioned. The first leg is most strongly affected. The second and third legs are slightly longer but also fail to form joints.

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
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
Comments
Comments

Etymology: 'stummelbein' is German for 'short leg'. Reversion analysis indicates that the P{Mcp-w#14} insertion is the cause of the mutant phenotype.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
AP-2stummelbein
TfAP-2stummelbein
dAP-2stummelbein
Name Synonyms
stummelbein
Secondary FlyBase IDs
    References (1)