FB2024_03 , released June 25, 2024
Allele: Hsap\NOTCH2NLCuN2CpolyG.UAS.GFP
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General Information
Symbol
Hsap\NOTCH2NLCuN2CpolyG.UAS.GFP
Species
H. sapiens
Name
FlyBase ID
FBal0385106
Feature type
allele
Associated gene
Hsap\NOTCH2NLC
Associated Insertion(s)
Carried in Construct
P{UAS-uN2CpolyG.GFP}
Key Links
Transgenic product class
trinucleotide_repeat_expansion
(Yu et al., 2022)
Mutagen
Nature of the Allele
Transgenic product class
trinucleotide_repeat_expansion
(Yu et al., 2022)
Mutagen
in vitro construct
(Yu et al., 2022)
Progenitor genotype
Carried in construct
P{UAS-uN2CpolyG.GFP}
Cytology
Description

UASt regulatory sequences drive expression of 'uN2C', a small upstream open reading frame (ORF) in the 5'UTR of the Hsap\NOTCH2NLC gene. The uN2C coding sequence contains an expanded poly-glycine repeat of 100 residues . The coding sequence is tagged at the C-terminal end with GFP.

(Yu et al., 2022)
Allele components
Component
Use(s)
Regulatory region(s)
UASt
Encoded product / tool
Hsap\NOTCH2NLC
Tagged with
GFP
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  neuronal intranuclear inclusion disease
      CEA
      (Yu et al., 2022)
      Modifiers Based on Experimental Evidence ( 1 )
      Disease
      Interaction
      References
      model of  neuronal intranuclear inclusion disease
      is exacerbated by ND-49RNAi.UAS.cUa
      (Yu et al., 2022)
      is exacerbated by ND-B14RNAi.UAS.cUa
      (Yu et al., 2022)
      Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
       
      Disease-implicated variant(s)
       
      This allele represents a human variant implicated in disease.
      (Yu et al., 2022)
      NOTCH2NLC:n.5'UTR[100GGC]
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      NOTCH2NLC, (GGC)n REPEAT EXPANSION, 5-PRIME UTR
      Associated human disease model(s)
      External database links
      ClinVar: 691867
      Comments concerning this variant
      Phenotypic 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\NOTCH2NLCuN2CpolyG.UAS.GFP
      Name Synonyms
      Secondary FlyBase IDs
        References (2)