FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Hsap\ALKR1275Q.UAS
Open Close
General Information
Symbol
Hsap\ALKR1275Q.UAS
Species
H. sapiens
Name
FlyBase ID
FBal0266008
Feature type
allele
Associated gene
Hsap\ALK
Associated Insertion(s)
Carried in Construct
P{UAS-hALK.R1275Q}
Also Known As
UAS-ALKR1275Q
Key Links
Transgenic product class
missense_variant
(Schönherr et al., 2011)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Schönherr et al., 2011)
Mutagen
in vitro construct
(Schönherr et al., 2011)
Progenitor genotype
Carried in construct
P{UAS-hALK.R1275Q}
Cytology
Description

UAS regulatory sequences drive expression of a mutated form of Hsap\ALK (amino acid replacement: R1275Q). An 898bp fragment preceeding the translation start site has been removed to increase expression efficiency in Drosophila.

(Schönherr et al., 2011)

Amino acid replacement: R1275Q.

(Schönherr et al., 2011)
Allele components
Component
Use(s)
Regulatory region(s)
UAS
Encoded product / tool
Hsap\ALK
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.
      (Schönherr et al., 2011)
      ALK:p.Arg1275Gln
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      ALK:p.Arg2075Gln
      Associated human disease model(s)
      External database links
      ClinVar: ALK_18083
      Comments concerning this variant
      Phenotypic Data
      Phenotypic Class
      Phenotype Manifest In
      Detailed Description
      Statement
      Reference

      Expression of Hsap\ALKR1275Q.Scer\UAS driven by Scer\GAL4GMR.PFa results in a fully penetrant rough eye phenotype.

      (Siaw et al., 2016)

      Expression of Hsap\ALKR1275Q.Scer\UAS under the control of Scer\GAL4GMR.PFa results in a rough eye phenotype. The regular hexagonal arrangement of ommatidia is disrupted and many interommatidial bristles are missing.

      (Schönherr et al., 2011)
      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 (3)
      Reported As
      Symbol Synonym
      Hsap\ALKR1275Q.Scer\UAS
      Hsap\ALKR1275Q.UAS
      hALKR1275Q
      (Schönherr et al., 2011)
      Name Synonyms
      Secondary FlyBase IDs
        References (4)