FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Abd-BM5
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General Information
Symbol
Dmel\Abd-BM5
Species
D. melanogaster
Name
FlyBase ID
FBal0033317
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
AbdBM5
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology

Polytene chromosomes normal.

Description

Amino acid replacement: ?119term.

Nucleotide substitution: C?T.

Stop codon in first class A exon.

Mutations within coding region: eliminate m function.

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

C16932677T

Amino acid change:

Q119term | Abd-B-PB; Q119term | Abd-B-PH

Reported amino acid change:

?119term

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. The amino acid substitution to a stop codon produces an Abd-B M protein of 118 amino acids instead of the normal 493.

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

The genital primordium in Abd-BM5 homozygous embryos lacks about four hdc-expressing cells, two in each of the two anterior clusters. Abd-BM5 female mutant clones exhibit transformation of the dorsal eighth tergite into an anterior tergite, while the genitalia structures are transformed to varying degrees into a structure resembling a sternite.

Normal numbers of the non-sexually dimorphic somatic gonadal precursor cells (SGPs) are specified in mutant embryos and they associate with the migrating germ cells. However, the gonads are often not as tightly compacted as in wild type. Gonads of mutant male embryos lack male-specific SGPs (which are present in wild-type male embryos) and resemble female gonads.

dMP2 and MP1 neurons appear to be generated throughout the ventral nerve cord in normal numbers in Abd-BM2/Abd-BM5 embryos. However, at stage 17, all dMP2 and MP1 neurons (including posterior ones) appear to undergo apoptosis (in wild-type embryos, the anterior dMP2 and MP1 neurons are lost by the late embryonic stage, but posterior dMP2 and MP1 neurons persist). Expression of Abd-BScer\UAS.cCa under the control of Scer\GAL4elav-C155 in late stage Abd-BM2/Abd-BM5 embryos results in the suppression of cell death normally seen in anterior dMP2 and MP1 neurons in wild-type late stage embryos.

In Abd-BM5/Df(3R)P115 mutant embryos, the boundaries between segments A6 and A7 and between A7 and A8 are partially fused.

Mutants lack posterior spiracles but form a well developed A8 ventral denticle belt.

An A7 segment forms in Abd-BM5/Abd-Biab8-D14 adult males.

abd-Ahs.PS Abd-BM5 heat induced embryos exhibit transformation of parasegments 10-13, parasegment 14 is wild type.

Parasegments 10--13 are transformed to parasegment 9 (FBrf0043917).

A5-A8 are transformed to A4, females lack genitalia, and there is a weak haploinsufficient transformation of A5-A8. Parasegments 10-13 are transformed to parasegment 9 in embryos.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

dMP2 and MP1 neurons are generated normally in Abd-BM5 Df(3L)H99 double homozygous embryos. In late stage Abd-BM5 Df(3L)H99 double homozygous embryos neither anterior nor posterior dMP2 and MP1 neurons undergo apoptosis.

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

m-r+, causes abd-A expression to be high in parasegment 13 from the extended germ band stage, with no expression in parasegments 14 or 15.

Absence of the 'm' element.

Genetically null for the Abd-B m function.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
References (32)