FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\spo1
Open Close
General Information
Symbol
Dmel\spo1
Species
D. melanogaster
Name
FlyBase ID
FBal0016044
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Amino acid replacement: I44T.

Nucleotide substitution: C132T.

Amino acid replacement: R138A.

Nucleotide substitution: G414A.

Amino acid replacement: F167S.

Nucleotide substitution: T500C.

Amino acid replacement: P203A.

Nucleotide substitution: C608A.

Amino acid replacement: S425N.

Nucleotide substitution: G1274A.

Amino acid replacement: G481E.

Nucleotide substitution: G1442A.

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

G5590777A

Reported nucleotide change:

G1442A

Amino acid change:

G481E | spo-PA; G481E | spo-PC

Reported amino acid change:

G481E

Comment:

Point mutation in an evolutionarily conserved heme-binding domain. 5 other amino acid changes were reported in the mutant but some of them do not result in the reported amino acid changes. This one is highlighted as a significant change.

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

7 to 16 hour homozygous embryos contain very low concentrations of both ecdysone and 20-hydroxyecdysone compared to control embryos. Mutants fail to make cuticle and show defects in morphogenetic movements during late embryogenesis that lead to a failure of head involution and defective midgut formation.

Larval mouth parts and denticles not differentiated.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Suppressed by
Statement
Reference
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference

Expression of Bmor\Cyp307a1Scer\UAS.T:Ivir\HA1 under the control of Scer\GAL4Act5C.PU rescues the lethality of spo1 homozygotes.

Complementation and Rescue Data
Comments

Expression of spoScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4Act5C.PU rescues the lethality of spo1 homozygotes.

Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (6)