FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\rho5
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General Information
Symbol
Dmel\rho5
Species
D. melanogaster
Name
FlyBase ID
FBal0017859
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
rholac1
Key Links
Nature of the Allele
Progenitor genotype
Associated Insertion(s)
Cytology
Description

P{lacW} is inserted in or downstream of the rho promoter, at the 5' end of the rho transciption unit.

Allele components
Component
Use(s)
Inserted element
Encoded product / tool
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

chordotonal organ | precursor & embryonic abdomen

embryonic head & external sensory organ

embryonic thorax & external sensory organ

Detailed Description
Statement
Reference

Embryos have only three ventral longitudinal muscle fibres per abdominal hemisegment, instead of the usual 4: muscle 7 fails to develop. Development of other muscle fibres in the dorsal region and the ventral oblique muscle fibres 14.1 and 14.2 are abnormal. Embryos also lack several of the midline glia in the CNS. In the absence of muscle fibre 7 motoneuron RP3 innervates the remaining muscle fibre 6 in 83% of embryos, in the remaining 17% the growth cone fails to synapse with muscle 6 but project distally, they do not synapse before death at state 17. Deletion of muscle 7 does not affect RP1 growth cone behaviour.

Similar to rho7M43 with respect to the PNS phenotype. Cuticular phenotype less severe than rho7M43 or rho6. CNS is apparently normal. Two of the five lateral chordotonal organs are missing. The chordotonal organ with the neuronal dendrite pointing ventrally can be missing from the ventral cluster. The es and md neurons in the abdominal segments are unaffected, though es organs in the head and thorax that are innervated by multiple neurons are reduced in number. Embryonic muscle pattern is abnormal. As well as the regular dorso-lateral muscle absences, ventral longitudinal muscles are also occasionally missing. Muscle attachment sites are sometimes relocated, with fibers attaching to the ventral midline.

weak allele embryonic lethal

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Suppressor of
Statement
Reference

rho5/rho[+] is a suppressor of visible | heat sensitive phenotype of HC2.hs

Phenotype Manifest In
Suppressor of
Statement
Reference

rho5/rho[+] is a suppressor of wing vein | ectopic | heat sensitive phenotype of HC2.hs

rho5/rho[+] is a suppressor of wing | heat sensitive phenotype of HC2.hs

Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Fails to complement
Partially rescued by

rho5 is partially rescued by rhoRyn

Comments

rho5 is both partially rescued by two copies of rhoRyn : 40% of such embryos hatch as viable larvae, with rescued cuticular phenotype. Rescued larvae do not survive to adulthood.

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

Bier.

Comments
Comments

Can revert to wild type under dysgenic conditions.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (6)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (5)