FB2025_01 , released February 20, 2025
Allele: Dmel\htlYY262
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General Information
Symbol
Dmel\htlYY262
Species
D. melanogaster
Name
FlyBase ID
FBal0057258
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: E588K. Nucleotide substitution: G1871A.

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

G18046114A

Reported nucleotide change:

G1871A

Amino acid change:

E603K | htl-PA; E603K | htl-PB; E603K | htl-PC

Reported amino acid change:

E588K

Comment:

The annotated and reported mutation locations differ by 15aa due to use of a different initiator methione.

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

htlYY262 homozygous embryos exhibit random loss of cardioblasts (both generic cardioblasts and ostial cardioblasts), as compared to controls.

Embryos zygotically mutant for htlYY262 exhibit defects in mesoderm layer formation during gastrulation. Differentiation of eve-positive dorsal mesoderm precursors is also affected in these embryos.

htlYY262/htlAB42 flies rescued to the pupal stage by expression of htlScer\UAS.cMa under the control of three drivers (Scer\GAL4Mz1277,Scer\GAL4Bx-MS1096 and Scer\GAL4twi.PB) gives axon guidance phenotypes in the head. Ocellar pioneer (OP) axons project into the epidermis, bristle mechanosensory (BM) axons fail to project into the brain, or stall in the epidermis or extend apart of epidermis.

Mesodermal cells show some dorsolateral migration in homozygous embryos, but fail to reach the dorsal-most epidermal cells in most segments.

Significant number of both dorsal somatic muscles and cardiac cells develop.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Enhanced by
Statement
Reference

htlYY262 has mesoderm phenotype, enhanceable by nst16923

htlYY262 has mesoderm phenotype, enhanceable by nstc04986

htlYY262 has mesoderm phenotype, enhanceable by Df(3L)ED4486

Additional Comments
Genetic Interactions
Statement
Reference

nst16923, nstc04986 or Df(3L)ED4486 zygotically enhance the reduced eve-positive dorsal mesoderm precursor phenotype of htlYY262 embryos.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

The addition of htlScer\UAS.cMa driven by Scer\GAL4twi.PB fails to rescue the lethality seen in htlYY262/htlAB42. However, when htlScer\UAS.cMa is driven by Scer\GAL4Mz1277, Scer\GAL4Bx-MS1096 and Scer\GAL4twi.PB concurrently, some escaper pupae do survive.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (9)