FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\hkbgurt
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General Information
Symbol
Dmel\hkbgurt
Species
D. melanogaster
Name
gurtelchen
FlyBase ID
FBal0239726
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

Amino acid replacement: R236H.

Nucleotide substitution: G707A.

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

G4345732A

Reported nucleotide change:

G707A

Amino acid change:

R236H | hkb-PA

Reported amino acid change:

R236H

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

Visceral mesoderm fails to elongate dorso-ventrally and remains belt shaped until the end of embryogenesis in mutant embryos. Somatic myogenesis appears unaffected in the mutant embryos.

hkbgurt/hkb2 embryos show the visceral mesoderm defects seen in hkbgurt embryos.

Visceral mesoderm cell identifies (fusion competent myoblasts and founder cells) are specified correctly in hkbgurt mutant embryos.

Epidermal morphology and hindgut development are normal in hkbgurt mutant embryos, but severe defects are seen in the foregut. The anterior midgut primordium does not form. Malpighian tubules fail to develop properly, forming a sac-like structure that also seems to include the remnants of the posterior midgut rudiment.

Stage 13 hkbgurt embryos show initial stretching of the visceral bands, as occurs in wild type, although the visceral bands of these embryos appear densely packed and contain many myotubes with a slightly angular orientation. Subsequent elongation of the visceral circular muscles does not occur in the mutant embryos and stage 15-16 hkbgurt embryos have strong defects in the visceral muscle. The determination of the longitudinal visceral muscle primordium at the posterior end of the mesoderm occurs normally in the mutant embryos. During later stages, anterior migration of longitudinal muscle cells and longitudinal muscle fusion occurs in the mutant embryos, as occurs in wild type.

The extracellular matrix shows a scattered appearance along the visceral muscle strands in stage 13-14 mutant embryos.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Fails to complement
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer

The "3B1-038" chromosome contain two mutations that affect visceral mesoderm development; hkbgurt and knod3B1-038. These mutations have been separated by meiotic recombination.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Symbol Synonym
Name Synonyms
gurtelchen
Secondary FlyBase IDs
    References (1)