FB2024_03 , released June 25, 2024
Allele: Dmel\pntP1-90
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General Information
Symbol
Dmel\pntP1-90
Species
D. melanogaster
Name
FlyBase ID
FBal0322762
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
pntP190
Key Links
Genomic Maps

Mutagen
Nature of the Allele
Progenitor genotype
Cytology
Description

Mutation affecting the pnt-P1 isoform. Indel in the P1-specific exon 1, resulting in a frameshift and premature stop codon that deletes the 445 C-terminal amino acids (including the Ets DNA-binding domain).

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

Appears to be a deletion of 13 bp and insertion of 8 (CTGCGACT) after amino acid 176 causing a net deletion of 5 bp. Leads to a frameshift and early translation termination.

Inserted_sequence:

CTGCGACT

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
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
Statement
Reference

pntP1-90 has decreased cell number | larval stage phenotype, enhanceable by btd[+]/btdXG

pntP1-90 has abnormal neuroanatomy | larval stage phenotype, enhanceable by btd[+]/btdXG

pntP1-90 has decreased cell number | larval stage phenotype, enhanceable by btd[+]/btdMD808

pntP1-90 has abnormal neuroanatomy | larval stage phenotype, enhanceable by btd[+]/btdMD808

Suppressed by
Phenotype Manifest In
Enhanced by
Statement
Reference
Suppressed by
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

btdXG/+ or btdMD808/+ enhances the loss of intermediate neural progenitors, but suppresses the increased number of Asense-negative type II neuroblasts, although (in the case of btdMD808/+) does not suppress the increased number of total neuroblasts seen in pntP1-90/pntP1-90 mutant larvae.

Df(2L)erm2/+ significantly enhances the increase in type II neuroblasts seen in pntP1-90/pntP1-90 mutant larvae.

Expression of ermScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4GMR9D11 significantly suppresses the increase in type II neuroblasts seen in pntP1-90/pntP1-90 mutant larvae.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
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)