FB2025_01 , released February 20, 2025
Allele: Hsap\DNAJC5L116Δ.UAS
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General Information
Symbol
Hsap\DNAJC5L116Δ.UAS
Species
H. sapiens
Name
FlyBase ID
FBal0358408
Feature type
allele
Associated gene
Hsap\DNAJC5
Associated Insertion(s)
Carried in Construct
M{UAS-hDNAJC5.L116Δ}
Key Links
Transgenic product class
inframe_deletion
(Imler et al., 2019)
Mutagen
Nature of the Allele
Transgenic product class
inframe_deletion
(Imler et al., 2019)
Mutagen
in vitro construct
(Imler et al., 2019)
Progenitor genotype
Carried in construct
M{UAS-hDNAJC5.L116Δ}
Cytology
Description

UAS regulates expression of Hsap\DNAJC5 containing the the single amino acid deletion L116Δ, which is causative of neuronal ceroid lipofuscinosis CLN4.

(Imler et al., 2019)
Allele components
Component
Use(s)
Regulatory region(s)
UAS
Encoded product / tool
Hsap\DNAJC5
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 ceroid lipofuscinosis 4
      CEA
      (Lee et al., 2023, Imler et al., 2019)
      Modifiers Based on Experimental Evidence ( 1 )
      Disease
      Interaction
      References
      model of  neuronal ceroid lipofuscinosis 4
      is ameliorated by Hsc70-4HMS00152
      (Imler et al., 2019)
      is ameliorated by Hsc70-4Δ356
      (Imler et al., 2019)
      is exacerbated by Syx1AUAS.cBa
      (Imler et al., 2019)
      is exacerbated by nSybUAS.EGFP
      (Imler et al., 2019)
      Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
       
      Disease-implicated variant(s)
       
      This allele represents a human variant implicated in disease.
      (Imler et al., 2019)
      DNAJC5:p.Leu116del
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      Associated human disease model(s)
      External database links
      ClinVar: DNAJC5_30893
      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 (0)
      Notes on Origin
      Discoverer
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (1)
      Reported As
      Symbol Synonym
      Hsap\DNAJC5L116Δ.UAS
      Name Synonyms
      Secondary FlyBase IDs
        References (3)