FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Hsap\APPC99.V717I.UAS.Exel.Tag:HA
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General Information
Symbol
Hsap\APPC99.V717I.UAS.Exel.Tag:HA
Species
H. sapiens
Name
FlyBase ID
FBal0256661
Feature type
allele
Associated gene
Hsap\APP
Associated Insertion(s)
Carried in Construct
P{UAS-APP.C99.V717I.HA.Exel}
Key Links
Transgenic product class
inframe_deletion
(Singh and Mahoney, 2011.2.17)
missense_variant
(Singh and Mahoney, 2011.2.17)
Mutagen
Nature of the Allele
Transgenic product class
inframe_deletion
(Singh and Mahoney, 2011.2.17)
missense_variant
(Singh and Mahoney, 2011.2.17)
Mutagen
in vitro construct
(Singh and Mahoney, 2011.2.17)
Progenitor genotype
Carried in construct
P{UAS-APP.C99.V717I.HA.Exel}
Cytology
Description

UAS drives expression of the C99 fragment of Hsap\APP carrying the familial Alzheimer's London" mutation (V717I -amino acid numbering based on Hsap\APP sequence) with the Hsap\APP signal peptide and a C-terminal tag consisting of three copies of Tag:HA.

(Singh and Mahoney, 2011.2.17)
Allele components
Component
Use(s)
Regulatory region(s)
UAS
Encoded product / tool
Hsap\APP
Tagged with
Tag:HA
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.
      (Singh and Mahoney, 2011.2.17)
      APP:p.Val717Ile
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      APP:p.Val642Ile
      Associated human disease model(s)
      External database links
      ClinVar: APP_18088
      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
      Complementation and Rescue Data
      Comments
      Images (0)
      Mutant
      Wild-type
      Stocks (2)
      Notes on Origin
      Discoverer
      Comments
      Comments

      Made by Exelixis, Inc.

      (Singh and Mahoney, 2011.2.17)
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (2)
      Reported As
      Symbol Synonym
      Hsap\APPC99.V717I.Scer\UAS.Exel.T:Ivir\HA1
      Hsap\APPC99.V717I.UAS.Exel.Tag:HA
      Name Synonyms
      Secondary FlyBase IDs
        References (2)