FB2024_03 , released June 25, 2024
Allele: Dmel\MhcD1
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General Information
Symbol
Dmel\MhcD1
Species
D. melanogaster
Name
FlyBase ID
FBal0097226
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Amino acid replacement: D623G.

Nucleotide substitution: A to G. Amino acid replacement: D to G. Mutation is in exon 10 at the base of the second loop (which is involved in actin binding) of the head domain.

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

A16777142G

Reported nucleotide change:

A?G

Amino acid change:

D623G | Mhc-PA; D623G | Mhc-PB; D623G | Mhc-PC; D623G | Mhc-PD; D623G | Mhc-PE; D623G | Mhc-PF; D623G | Mhc-PG; D623G | Mhc-PH; D623G | Mhc-PI; D623G | Mhc-PK; D623G | Mhc-PL; D623G | Mhc-PM; D623G | Mhc-PN; D623G | Mhc-PO; D623G | Mhc-PP; D623G | Mhc-PQ; D623G | Mhc-PR; D623G | Mhc-PS; D623G | Mhc-PT; D623G | Mhc-PU; D623G | Mhc-PV

Reported amino acid change:

D623G

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

Heterozygotes show defects in flight ability.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Suppressor of
Statement
Reference

MhcD1/Mhc[+] is a suppressor of visible phenotype of up101

MhcD1/Mhc[+] is a suppressor of visible phenotype of wupAhdp-2

MhcD1 is a suppressor of visible | recessive phenotype of wupAhdp-2

NOT Suppressor of
Statement
Reference

MhcD1/Mhc12 is a non-suppressor of visible phenotype of wupAhdp-3

Other
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

The defects seen in wupAhdp-2 flies are suppressed by MhcD1/+; 7% of the double mutant adults have an upheld wing phenotype and 93% hold their wings in the normal position. The indirect flight muscle fibres have normal morphology. The defects seen in up101 flies are suppressed by MhcD1/+; 4% of the double mutant adults hold their wings down, 18% have an upheld wing phenotype and 78% hold their wings in the normal position. The indirect flight muscle fibres have normal morphology.

Dominant suppressor of the heldup wing phenotype of wupAhdp-2; wupAhdp-2/Y ; MhcD1/+ males have a near normal wing position, but cannot jump or fly. Dorsolongitudinal muscle (DLM) fibres a to d appear almost normal in these flies, but DLM muscles e and f are collapsed. The number of thick filaments per fibril is reduced compared to wild type. wupAhdp-2/Y ; MhcD1/MhcD41 flies can jump. wupAhdp-2/Y ; MhcD1/MhcD62 flies have a high frequency of double thick filaments in the DLMs.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Partially complements
Fails to complement
Not rescued by
Comments

MhcD1 is occasionally viable in combination with Mhc1.

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

Selected as: a dominant suppressor of wupAhdp-2.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (3)