FB2024_03 , released June 25, 2024
Allele: Dmel\hry22
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General Information
Symbol
Dmel\hry22
Species
D. melanogaster
Name
FlyBase ID
FBal0005339
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
hC1
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology

Polytene chromosomes normal.

Description

Nucleotide substitution: C?T.

Amino acid replacement: R43term.

run protein produced is truncated, terminating in the basic region.

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

C8677399T

Reported nucleotide change:

C?T

Amino acid change:

R43term | h-PA; R43term | h-PB

Reported amino acid change:

R43term

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

Homozygous embryos have abnormally shaped salivary glands; 15% have elongated, branched lumens, 40% have elongated, expanded lumens, 37.5% have short, expanded lumens, 2.5% show no invagination and 5% are normal (elongated, unbranched lumens). h22/h674 embryos have salivary glands with either branched or expanded lumens.

h22/groE48 double heterozygotes differentiate ectopic microchaete along the wing vein 2.

emc1 h22 clones display differentiated photoreceptors that arise in a more anterior position that in adjacent wild type tissue, the morphogenetic furrow has been shifted anteriorly.

Extra neuron mutant.

Legs from hcosh; h-/h- adults show a bristle patterning defect that correlates with the expression pattern of h in pupal leg imaginal discs.

h22 mutant clones in the eye have very few defective ommatidia.

Class IV allele: has a strong segmentation phenotype either when homozygous or in trans with h25, and fails to complement the bristle phenotype of h1.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Other
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

emc1 h22 double homozygous clones in the eye imaginal disc that intersect the morphogenetic furrow from the posterior, have an anteriorly shifted morphogenetic furrow.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer
Comments
Comments

Selected on the basis of its failure to complement the bristle phenotype of either h1 or h2.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (5)
References (17)