FB2026_02 , released June 18, 2026
Allele: Hsap\PABPN1dm.17ala.UAS
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General Information
Symbol
Hsap\PABPN1dm.17ala.UAS
Species
H. sapiens
Name
FlyBase ID
FBal0196240
Feature type
allele
Associated gene
Hsap\PABPN1
Associated Insertion(s)
Carried in Construct
P{UAS-PABPN1.17ala-dm}
Key Links
Transgenic product class
missense_variant
(Chartier et al., 2006)
short_tandem_repeat_expansion
(Chartier et al., 2006)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Chartier et al., 2006)
short_tandem_repeat_expansion
(Chartier et al., 2006)
Mutagen
in vitro construct
(Chartier et al., 2006)
Progenitor genotype
Carried in construct
P{UAS-PABPN1.17ala-dm}
Cytology
Description

Amino acid replacement: Y182A.

(Chartier et al., 2006)

UASt regulatory sequences drive expression of an altered form of Hsap\PABPN1 which encodes 17 alanine residues following the initial methionine, instead of the wild-type number of 10, and which carries two mutations (Y182A and F222A) in the RRM domain.

(Chartier et al., 2006)

Amino acid replacement: F222A.

(Chartier et al., 2006)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Hsap\PABPN1
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)
       
      Phenotypic Data
      Phenotypic Class
      Phenotype Manifest In
      Detailed Description
      Statement
      Reference

      Expression of Hsap\PABPN1dm.17ala.Scer\UAS under the control of Scer\GAL4Mhc.PW causes no, or a very low number of, flies with abnormal wing position. The musculature of these flies appears to be unaffected, and nuclear morphology is normal.

      (Chartier et al., 2006)
      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 (0)
      Notes on Origin
      Discoverer
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (2)
      Reported As
      Symbol Synonym
      Hsap\PABPN1dm.17ala.Scer\UAS
      Hsap\PABPN1dm.17ala.UAS
      Name Synonyms
      Secondary FlyBase IDs
        References (1)