FB2026_02 , released June 18, 2026
Allele: Dmel\GPHRk34
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General Information
Symbol
Dmel\GPHRk34
Species
D. melanogaster
Name
FlyBase ID
FBal0294784
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

Nucleotide substitution: C?T.

Amino acid replacement: P91L.

There is a missense mutation in the GPHR coding region that substitutes a highly conserved Proline to a Leucine in the third transmembrane domain of the protein.

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

C15200698T

Reported nucleotide change:

C?T

Amino acid change:

P91L | GPHR-PA

Reported amino acid change:

P91L

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

GPHRk34 larval escapers survive through the pupal stage to give rise to pharate adults that are significantly smaller and lighter than control animals. While GPHRk34 mutant and wild-type larvae grow equally until late mid-L3 stage (96 hr after egg deposition), GPHRk34 mutant larvae show growth deceleration at late L3. By late L3 and pupal stages, size differences between wild-type and mutant siblings are obvious. In addition, the onset of both pupariation and adult emergence are delayed in GPHRk34 mutants.

Both cell size and number are reduced in GPHRk34 homozygous and GPHRk34/Df(2R)ED2426 mutant adult wing blades.

GPHRk34 homozygous mutant mitotic wing imaginal disc clones grow and divide to clones of a similar size as wild-type clones. These cells do not show differences in cell division or size, compared to controls. Although GPHRk34 mutant larvae (120 hrs after egg deposition) display salivary gland cells with reduced nuclei size when compared to controls, no obvious differences in nuclei size are observed between GPHRk34 mutant MARCM salivary gland cell clones and wild-type cells.

GPHRk34 mutants exhibit severe endoplasmic reticulum and Golgi disorganisation.

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference

Ubiquitous expression of Hsap\GPR89AScer\UAS.cCa under the control of Scer\GAL4da.G32 is sufficient to fully suppress the growth defects and developmental lethality seen in GPHRk34 mutants.

Ubiquitous expression of Zzzz\GphrScer\UAS.cCa under the control of Scer\GAL4da.G32 is sufficient to fully suppress the growth defects and developmental lethality seen in GPHRk34 mutants.

Complementation and Rescue Data
Comments

Ubiquitous, neuronal or gut expression of GPHRScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4da.G32 is sufficient to fully rescue the growth defects and developmental lethality seen in GPHRk34 mutants. Muscle expression (under the control of Scer\GAL4Mef2.PR does not rescue.

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Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
GPHRk34
Name Synonyms
Secondary FlyBase IDs
    References (1)