FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\oc2
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General Information
Symbol
Dmel\oc2
Species
D. melanogaster
Name
FlyBase ID
FBal0013200
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
otdJA101, otd2
Key Links
Mutagen
Nature of the Allele
Progenitor genotype
Cytology
Description

Small deletion.

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

The protocerebral brain anlage fails to develop in mutants and the preoral brain commissure is not formed.

The protocerebral brain anlage fails to develop in homozygous embryos, and the preoral brain commissure is missing or severely reduced. Ubiquitous overexpression of ochs.PR in homozygous embryos at stage 7-8 results in restoration of anterior brain morphology in over half the heat shocked embryos. Rescue of the embryonic brain phenotype by overexpression of ochs.PR is not possible after stage 8. Ubiquitous overexpression of Hsap\OTX2hs.PN in homozygous embryos at stage 7-8 results in restoration of anterior brain morphology in 45% of heat shocked embryos. Ubiquitous overexpression of Hsap\OTX1hs.PN in homozygous embryos at stage 7-8 results in restoration of anterior brain morphology in over one-fifth of heat shocked embryos. Rescue of the embryonic brain phenotype by overexpression of ochs.PR, Hsap\OTX1hs.PN or Hsap\OTX2hs.PN is not possible after stage 8. Homozygous embryos have deranged connectives and fused commissural axon tracts in the ventral nerve cord. This phenotype can be rescued by ubiquitous overexpression of ochs.PR at stage 10-11. The phenotype can be rescued in 100% of cases by ubiquitous overexpression of Hsap\OTX2hs.PN at stage 10-11. The phenotype can be rescued in over 90% of cases by ubiquitous overexpression of Hsap\OTX1hs.PN at stage 10-11. Rescue is not seen if ochs.PR, Hsap\OTX1hs.PN or Hsap\OTX2hs.PN is expressed before stage 10 or after stage 11.

Neuromere b1 is absent or reduced in all embryos.

Median ocellus is displaced anteriorly and is smaller. The pattern of interocellar and ocellar bristles is disturbed. The distance between the two lateral ocelli and between the two postvertical bristles is increased. Phenotypic series from the strongest to weakest oc allele: ocdb/ocdb > oc1/oc+ > ocγa1/oc+ > oc2/oc+ > oc1/oc1 > ocγa1/ocγa1 > oc2/oc1 > oc2/ocγa1.

The dorsal arms of the head skeleton are absent or fragmented in mutant embryos. The antennal segment is missing.

Defects in head development and segmental patterning. Abnormal neuropil. Aberrant commissure formation in each segment. The disappearance of neurons labelled by a P{A92}45C demonstrate that cell death is restricted to identified neurons associated with the midline of the CNS.

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

oc2 has embryonic brain & commissure phenotype, suppressible by Hror\Otxhs.PA

oc2 has embryonic brain & commissure phenotype, suppressible by Hsap\OTX2hs.PN

Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference

The embryonic brain defects of oc2 animals are partially rescued by Hsap\OTX2hs.PN or Hror\Otxhs.PA.

Complementation and Rescue Data
Partially rescued by

oc2 is partially rescued by ochs.PR

oc2 is partially rescued by ochs.PR

Comments

non-complementing allele

Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer

Lefevre.

Comments
Comments

Less than 50% of wild type number of ventral epidermal cells expressing P{lacZ}BP28 are evident in mutant embryos.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (5)
References (19)