FB2025_01 , released February 20, 2025
Allele: Hsap\NRXN1L893V.UAS.Tag:FLAG
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General Information
Symbol
Hsap\NRXN1L893V.UAS.Tag:FLAG
Species
H. sapiens
Name
FlyBase ID
FBal0370777
Feature type
allele
Associated gene
Hsap\NRXN1
Associated Insertion(s)
Carried in Construct
P{UAS-hNRXN1.L893V}
Key Links
Transgenic product class
missense_variant
(Liu et al., 2021)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Liu et al., 2021)
Mutagen
in vitro construct
(Liu et al., 2021)
Progenitor genotype
Carried in construct
P{UAS-hNRXN1.L893V}
Cytology
Description

UASt regulates expression of Hsap\NRXN1 bearing the L893V mutation (found in Autism spectrum disorder patients) with a C-terminal Tag:FLAG tag.

(Liu et al., 2021)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Hsap\NRXN1
Tagged with
Tag:FLAG
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 ( 1 )
      Disease
      Evidence
      References
      model of  autism spectrum disorder
      CEA
      (Liu et al., 2021)
      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.
      (Liu et al., 2021)
      NRXN1:p.Leu893Val
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      many
      Associated human disease model(s)
      External database links
      Comments concerning this variant
      Phenotypic Data
      Phenotypic Class
      Phenotype Manifest In
      Detailed Description
      Statement
      Reference

      The expression of Hsap\NRXN1L893V.UAS.Tag:FLAG under the control of Scer\GAL4elav.PU or Scer\GAL4tim.PE leads to circadian defects: Scer\GAL4elav.PU-driven expression induces an increased morning activity, as well as decreased day-time sleep, with more but shorter day-time sleep bouts, and increased night-time sleep, with fewer but longer sleep bouts; Scer\GAL4tim.PE-driven expression induces increased evening activity and increased period, as well as fewer but longer total and night-time sleep bouts.

      (Liu et al., 2021)
      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 (1)
      Reported As
      Symbol Synonym
      Hsap\NRXN1L893V.UAS.Tag:FLAG
      Name Synonyms
      Secondary FlyBase IDs
        References (2)