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General Information
Symbol
Dmel\pnt1230
Species
D. melanogaster
Name
FlyBase ID
FBal0035441
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Nature of the Allele
Mutations Mapped to the Genome
 
Type
Location
Additional Notes
References
Associated Sequence Data
DNA sequence
Protein sequence
 
 
Progenitor genotype
Cytology
Nature of the lesion
Statement
Reference

Small deletion that removes 5' flanking sequences and most of exon 1.

Deletion from within the P-element that extends distally.

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 )
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

pnt1277/pnt1230 eye discs show polarity defects (10% of ommatidial clusters are inverted and 9% are symmetrical).

pnt1230/pntΔ88 eye discs show chirality defects in 26.4% of ommatidial clusters.

Homozygous wing discs have a reduced pouch size compared to wild type.

Homozygous clones in the eye lack R7 and frequently R1 and R6 cells in most ommatidia.

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

pnt[+]/pnt1230 is a suppressor of visible phenotype of Scer\GAL4Tub.PU, cswN308D.UASp

Phenotype Manifest In
Suppressor of
Statement
Reference

pnt[+]/pnt1230 is a suppressor of wing vein | ectopic phenotype of Scer\GAL4Tub.PU, cswN308D.UASp

pnt1230 is a suppressor of phenotype of JraAsp.hs.sev

Additional Comments
Genetic Interactions
Statement
Reference

pntΔ88/pnt1277 or pnt1230/pnt1277 completely suppresses the ectopic R7 rough eye phenotype of JraAsp.hs.sev.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
Comments
Comments

Allelic series of pnt allele that affect the P2 transcript: pnt1277 < pnt1202 < pnt1208 < pnt1230 <= pntT9 < pntT5.

P2-specific mutation.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (8)