FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Vangstbm-153
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General Information
Symbol
Dmel\Vangstbm-153
Species
D. melanogaster
Name
FlyBase ID
FBal0088604
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
stbm153, Vang153
Key Links
Genomic Maps

Allele class
Mutagen
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

7bp deletion starting at nucleotide 614, causing a frameshift at amino acid 205.

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

Reported to be a 7bp deletion starting at nucleotide 614 causing a frame shift at aa 205; position of mutation on reference sequence inferred by FlyBase curator (using A of ATG of GB:AF044208 as position 1).

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

38 +/- 6.9% of ommatidia show defects in planar cell polarity in homozygotes.

Many Vangstbm-153 ommatidia over- or under-rotate; the variance (s.d.) in degree of rotation is greater than in wild type in adult eyes.

Homozygotes show defects in ommatidial polarity.

20% of Vangstbm-153 homozygous embryos fail to hatch, exhibiting a phenotype similar to unfertilized eggs. 81% of Vangstbm-7-6/Vangstbm-153 embryos fail to hatch, exhibiting a phenotype similar to unfertilized eggs. Approximately 23% of Vangstbm-7-6/Vangstbm-153 embryos are capable of reaching the 2-5 hour stage of development.

Homozygotes exhibit a range of polarity defects in the eye. 39.8% of ommatidia show polarity defects.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
Enhancer of
Statement
Reference
NOT Enhancer of
Statement
Reference

Vangstbm-153/Vang[+] is a non-enhancer of visible | adult stage phenotype of Nab2EP3716, Scer\GAL4GMR.PU

NOT Suppressor of
Statement
Reference

Vangstbm-153/Vang[+] is a non-suppressor of visible | adult stage phenotype of Nab2EP3716, Scer\GAL4GMR.PU

Vangstbm-153/Vang[+] is a non-suppressor of decreased size | adult stage phenotype of Nab2EP3716, Scer\GAL4GMR.PU

Phenotype Manifest In
Enhanced by
Statement
Reference

Vangstbm-153 has ommatidium phenotype, enhanceable by scrib[+]/scrib673

Vangstbm-153 has ommatidium phenotype, enhanceable by scrib[+]/scrib1

Vangstbm-153 has ommatidium phenotype, enhanceable by bdg164/bdg164

Vangstbm-153 has ommatidium phenotype, enhanceable by stanfrz3

Vangstbm-153 has ommatidium phenotype, enhanceable by pk1

NOT Enhanced by
Statement
Reference

Vangstbm-153 has ommatidium phenotype, non-enhanceable by dlg1[+]/dlg114

Vangstbm-153 has ommatidium phenotype, non-enhanceable by dlg1[+]/dlg118

Vangstbm-153 has ommatidium phenotype, non-enhanceable by dlg1[+]/dlg113

Vangstbm-153 has ommatidium phenotype, non-enhanceable by dlg1[+]/dlg1w55

Vangstbm-153 has ommatidium phenotype, non-enhanceable by l(2)gl4w3/l(2)gl[+]

Vangstbm-153 has ommatidium phenotype, non-enhanceable by par-6[+]/par-6Δ226

Vangstbm-153 has ommatidium phenotype, non-enhanceable by baz4/baz[+]

Vangstbm-153 has ommatidium phenotype, non-enhanceable by sdtXP/sdt[+]

Suppressed by
Statement
Reference

Vangstbm-153 has ommatidium phenotype, suppressible by fred[+]/fredH24

NOT suppressed by
Statement
Reference

Vangstbm-153 has ommatidium phenotype, non-suppressible by sdtXP/sdt[+]

Vangstbm-153 has ommatidium phenotype, non-suppressible by dlg1[+]/dlg114

Vangstbm-153 has ommatidium phenotype, non-suppressible by dlg1[+]/dlg118

Vangstbm-153 has ommatidium phenotype, non-suppressible by dlg1[+]/dlg113

Vangstbm-153 has ommatidium phenotype, non-suppressible by dlg1[+]/dlg1w55

Vangstbm-153 has ommatidium phenotype, non-suppressible by l(2)gl4w3/l(2)gl[+]

Vangstbm-153 has ommatidium phenotype, non-suppressible by par-6[+]/par-6Δ226

Vangstbm-153 has ommatidium phenotype, non-suppressible by baz4/baz[+]

Enhancer of
Statement
Reference

Vangstbm-153 is an enhancer of ommatidium phenotype of stanfrz3

NOT Enhancer of
Statement
Reference

Vangstbm-153/Vang[+] is a non-enhancer of eye phenotype of Nab2EP3716, Scer\GAL4GMR.PU

NOT Suppressor of
Statement
Reference

Vangstbm-153/Vang[+] is a non-suppressor of eye phenotype of Nab2EP3716, Scer\GAL4GMR.PU

Other
Additional Comments
Genetic Interactions
Statement
Reference

Heterozygosity for scrib1 or scrib673 enhances the frequency of ommatidia that show planar cell polarity defects in Vangstbm-153 homozygotes.

Heterozygosity for dlg114, dlg118, dlg113, dlg1w55, l(2)gl4w3, par-6Δ226, baz4 or sdtXP has no effect on the frequency of ommatidia that show planar cell polarity defects in Vangstbm-153 homozygotes.

fredH24 dominantly suppresses the phenotype of mis-rotation of ommatidia that is seen in Vangstbm-153 animals.

Homozygosity for bdg164 enhances the ommatidial polarity defects caused by homozygosity for Vangstbm-153.

32.9% of ommatidia in stanfrz3/stanfrz3, Vangstbm-153/+ animals exhibit polarity defects in the eye. 63.7% of ommatidia in stanfrz3/stanfrz3, Vangstbm-153/Vangstbm-153 animals exhibit polarity defects in the eye. They also have missing photoreceptor cells. 49.7% of ommatidia in pk1/pk1, Vangstbm-153/Vangstbm-153 animals exhibit polarity defects in the eye.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Partially rescued by
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (6)
References (11)