FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Fam921
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General Information
Symbol
Dmel\Fam921
Species
D. melanogaster
Name
FlyBase ID
FBal0358344
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Mutagen
Nature of the Allele
Progenitor genotype
Cytology
Description

294bp deletion that removes all of exon 2 and part of exon 3 of Fam92. This results in a frameshift that is predicted to produce a truncated protein retaining 47 residues from the wild-type protein and 39 residues translated from the frameshifted open reading frame.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Comment:

294bp deletion that removes all of exon 2 and part of exon 3 of Fam92. This results in a frameshift that is predicted to produce a truncated protein consisting of the first 47 residues of Fam92 folowed by 39 novel amino acids.

Reported_genomic_loc:

2L_r6:12425125..12425420

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

Fam921 homozygotes and Fam921/Df(2L)Exel6033 transheterozygotes show impaired geotaxis response in bang assays compared to Fam921 heterozygous controls, as only a few files reach the top of the tube after 30s. They also show severely reduced male fertility.

The chordotonal neurons of Fam921 homozygous scolopidia occasionally show fewer cilia and axonemal structure defects such as lack of microtubule doublets, excess accumulation of dense material beneath the ciliary membrane and deformation of the membrane. Most transitional zones show normal ultrastructure, but a few show incomplete radial symmetry and accumulate material (as observed for cilia). Linkers connecting the axoneme to the membrane can still be observed.

Fam921 testes showed a moderate dispersion of the nuclei along cysts and altered migration of sperm individualization complexes. Round spermatids exhibit axonemal defects, including missing microtubule central pairs and/or doublets, broken symmetry with each part of the axoneme being relocated along the mitochondria, or missing axonemes; some spermatids also exhibit aberrant growth of axonemal microtubules. Fam921 spermatocytes exhibit some undocked centrioles, as well as irregular distal end or microtubules extending from the centriole tip.

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Partially rescued by
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (2)