FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Rtel1xp171
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General Information
Symbol
Dmel\Rtel1xp171
Species
D. melanogaster
Name
FlyBase ID
FBal0370210
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

A premature stop codon (C-T mutation) disrupting base 2065 of the coding sequence (CDS), which locates in the conserved Helicase_C_2 domain.

Amino acid replacement: Q689term.

Nucleotide substitution: C2065T.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Nucleotide change:

C5750203T

Reported nucleotide change:

C2065T

Amino acid change:

Q689term | Rtel1-PA; Q689term | Rtel1-PB

Reported amino acid change:

Q689term

Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
Expression Data
Reporter Expression
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Reference
 
Marker for
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Reporter construct used in assay
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Disease-implicated variant(s)
 
Phenotypic Data
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Phenotypic Class
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Genetic Interactions
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Xenogenetic Interactions
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Complementation and Rescue Data
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Stocks (0)
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External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Rtel1xp171
Name Synonyms
Secondary FlyBase IDs
    References (1)