FB2024_03 , released June 25, 2024
Allele: Dmel\hd1
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General Information
Symbol
Dmel\hd1
Species
D. melanogaster
Name
FlyBase ID
FBal0004710
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
hd272-9
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: G463D.

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

G5372994A

Amino acid change:

G463D | hd-PA; G463D | hd-PB

Reported amino acid change:

G463D

Comment:

Site of nucleic acid difference inferred by FlyBase based on reported amino acid change

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 ( 1 )
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

Females homozygous for hd1 or transheterozygous for hd1/Df(3R)3-4 produce eggs with severely thin shells that dehydrate and collapse after they are laid.

Embryos from transheterozygous hd1/Df(3R)3-4 females arrest during the first few nuclear cleavage cycles.

Embryos from transheterozygous hd1/Df(3R)3-4 females expressing hdUAS.cBa under the control of Scer\GAL4c323 arrest during the first few nuclear cleavage cycles and have chromatin and centrosome abnormalities such as: chromatin bridges between nuclei, misshaped or multipolar spindles and an excess of centrosomes, either freed from the mitotic spindle or accumulated at spindle poles.

Early cleavage divisions in embryos homozygous for hdEGFP in a hd1/Df(3R)3-4 background appear normal, with mitotic defects becoming apparent during embryonic cycles 8/9.

hd1 and hd1/Df(3R)3-4 females lay eggs with thin shells that do not hatch. BrdU incorporation shows that hd1 follicle cell nuclei have a severe defect in amplification.

Egg shells produced by homozygous females extremely disrupted. Deficiency of endochorionic material. All six chorion proteins and their mRNA's present at reduced levels; deficiency in the level of chorion-gene amplification in follicle cells.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
NOT suppressed by
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Partially rescued by

hd1/Df(3R)3-4 is partially rescued by hdEGFP

Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer

Nusslein-Volhard.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (3)