FB2026_02 , released June 18, 2026
Allele: Dmel\LanB2knod
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General Information
Symbol
Dmel\LanB2knod
Species
D. melanogaster
Name
knodel
FlyBase ID
FBal0239727
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Nucleotide substitution: C?T.

Amino acid replacement: R948term.

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

C9621136T

Reported nucleotide change:

C?T

Amino acid change:

R948term | LanB2-PA; R948term | LanB2-PB

Reported amino acid change:

R948term

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

Homozygotes die at the end of embryogenesis.

LanB2knod, LanB2knod/LanB2d5A1 and LanB2knod/Df(3L)Exel6114 stage 16 embryos have a one-chambered, "dumpling-shaped" midgut and often have local accumulations and gaps in the visceral muscles.

LanB2knod/LanB2d5A1 embryos lack single somatic muscles at random positions. The ventral oblique muscles in the four anterior segments are not attached to their tendon sites or are completely missing.

The contact between the pericardial cells and the heart tube is lost in mutant embryos, resulting in the dissociation of pericardial cells.

The fat body shows local disruptions in late stage embryos and partially fails to attach to the tip of the incorrectly migrate salivary gland.

The extracellular matrix that surrounds the midgut is scattered in late LanB2knod embryos and appears only loosely attached to the midgut surface (in contrast to the close association seen in wild type).

Stage 13 LanB2knod/LanB2d5A1 embryos show disordered stretching of visceral myotubes.

Stage 13 LanB2knod embryos show a delay in the fusion of the anterior and posterior midgut primordia.

The migration of longitudinal visceral muscles along the visceral mesoderm is reduced compared to wild type in stage 12 LanB2knod embryos and the mutant migrating muscle cells have an aberrant shape.

Mutants show defects in visceral mesoderm development.

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
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 (4)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (3)