FB2025_02 , released April 17, 2025
Allele: Hsap\IMMTC17F.UAS.Tag:MYC
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General Information
Symbol
Hsap\IMMTC17F.UAS.Tag:MYC
Species
H. sapiens
Name
FlyBase ID
FBal0341852
Feature type
allele
Associated gene
Hsap\IMMT
Associated Insertion(s)
Carried in Construct
P{UAS-hIMMT.C17F.MYC}
Key Links
Transgenic product class
missense_variant
(Tsai et al., 2018)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Tsai et al., 2018)
Mutagen
in vitro construct
(Tsai et al., 2018)
Progenitor genotype
Carried in construct
P{UAS-hIMMT.C17F.MYC}
Cytology
Description

UASt regulatory sequences drive expression of Hsap\IMMT carrying a mutation (C17F) found in patients with Parkinson's disease, tagged with Tag:MYC.

(Tsai et al., 2018)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Hsap\IMMT
Tagged with
Tag:MYC
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Variant Molecular Consequences
Associated Sequence Data
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
 
UniProtKB/Swiss-Prot
    UniProtKB/TrEMBL
      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)
       
      This allele represents a human variant implicated in disease.
      (Tsai et al., 2018)
      IMMT:p.Cys17Phe
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      Associated human disease model(s)
      External database links
      Comments concerning this variant
      Phenotypic Data
      Phenotypic Class
      Phenotype Manifest In
      Detailed Description
      Statement
      Reference
      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

      The expression of Hsap\IMMTC17F.UAS.Tag:MYC under the control of Scer\GAL4Act.PU in a MitofilinLL02849 heterozygous background leads to severe lethality before adulthood, leads to a frequent "onion"-like mitochondrial phenotype in larval body wall muscles and leads to impaired larval crawling ability.

      (Tsai et al., 2018)
      Complementation and Rescue Data
      Comments
      Images (0)
      Mutant
      Wild-type
      Stocks (0)
      Notes on Origin
      Discoverer
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (1)
      Reported As
      Symbol Synonym
      Hsap\IMMTC17F.UAS.Tag:MYC
      Name Synonyms
      Secondary FlyBase IDs
        References (2)