FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Mmus\Tbc1d8bG39R.UAS.Tag:HA
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General Information
Symbol
Mmus\Tbc1d8bG39R.UAS.Tag:HA
Species
M. musculus
Name
FlyBase ID
FBal0391088
Feature type
allele
Associated gene
Mmus\Tbc1d8b
Associated Insertion(s)
Carried in Construct
M{UAS-mTbc1d8b.G39R.HA}
Transgenic product class
missense_variant
(Milosavljevic et al., 2022)
Mutagen
Nature of the Allele
Transgenic product class
missense_variant
(Milosavljevic et al., 2022)
Mutagen
in vitro construct
(Milosavljevic et al., 2022)
Progenitor genotype
Carried in construct
M{UAS-mTbc1d8b.G39R.HA}
Cytology
Description

UAS regulatory sequences drive expression of a Mmus\Tbc1d8b cDNA, mutated to carry a G39R amino acid replacement. This change is equivalent to a variant in the orthologous human TBC1D8B gene that has been identified in patients with nephrotic syndrome.

(Milosavljevic et al., 2022)

The coding sequence is tagged at the C-terminal end with Tag:HA.

(Milosavljevic et al., 2022)
Allele components
Component
Use(s)
Regulatory region(s)
UAS
Encoded product / tool
Mmus\Tbc1d8b
Tagged with
Tag:HA
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  nephrotic syndrome type 20
      CEA
      (Milosavljevic et al., 2022)
      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.
      (Milosavljevic et al., 2022)
      TBC1D8B:p.Gly39Arg
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      Associated human disease model(s)
      External database links
      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
      Mmus\Tbc1d8bG39R.UAS.Tag:HA
      Name Synonyms
      Secondary FlyBase IDs
        References (2)