FB2024_03 , released June 25, 2024
Allele: Dmel\dppH48
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General Information
Symbol
Dmel\dppH48
Species
D. melanogaster
Name
FlyBase ID
FBal0003061
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
dppHin48, dpp48
Key Links
Mutagen
Nature of the Allele
Mutagen
Progenitor genotype
Cytology

Polytene chromosomes normal.

Description
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
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

dppH61/dppH48 embryos show loss of dorsal tissue and expansion of the lateral denticle bands into dorsal regions. Head involution defects result in extruded globular structures at the anterior of the embryo.

Entire larval cuticle is ventralised. In dppH48; CrebAwR7 larvae the entire cuticle is lateralised.

Heterozygotes produce a variable number (0 to 150) of amnioserosa cells. The average number of amnioserosa cells produced is not altered if the embryos are also carrying 2 or 3 copies of tsgtwi.PM.

Homozygous clones induced in first instar larvae produce abnormalities in the dorsal side of the leg. Pattern elements from the dorsal side are missing, and may or may not be replaced with a duplicate version of the remaining ventral part of the leg. Duplications are arranged as mirror images. Cells from non-mutant territory surrounding the clone may also show defects, indicating that dpp acts non-autonomously.

Double mutants of dppH48 with sogYL26 or sog1 have phenotypes identical to that of the dpp mutant alone.

Despite effects on the global morphology of the embryo the proventriculus still forms. Compared to wild type more cells move into the proventriculus and an extra budding zone in the foregut epithelium near the proventriculus can be seen in some embryos.

Fail to complete germ band extension, die with strong ventralized phenotype and no dorsal derived epidermis.

Homozygotes have a ventralized embryonic phenotype: normally ventral epidermal pattern elements are present ventrally and dorsally.

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
Comments

Allele class: Hin

Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer
Comments
Comments

Haploinsufficient allele of dpp.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
References (21)