Version: 8.0.0
Date: Tue Jan 28 2025
mei-41D5
FB:FBal0012156
Allele of mei-41
Drosophila melanogaster
SummaryTransgenic ConstructsGenomic Variant InformationVariant Molecular ConsequencesPhenotypesDisease Associations
Allele/Variant

mei-41D5

Species
Drosophila melanogaster
Symbol
mei-41D5
Category
allele
Allele of gene
mei-41
Transgenic Constructs
None
Synonyms
  • D5
  • mei-41[D5]
Description
In addition to the P2159L amino acid replacement, which may cause the mutant phenotype, a number of additional amino acid changes are present compared to the U34925 mei-41 GenBank sequence (these "common" mutations are also present in other mei-41 mutant alleles, possibly due to variability present in the mutagenised population). Amino acid replacement: P2159L. Nucleotide substitution: C8924T.
Additional Information
Literature

Transgenic Constructs

No data available

Genomic Variant Information

No data available

Variant Molecular Consequences

No data available

Phenotypes

Phenotype
Annotation details
Source
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    Disease Associations

    Association
    Disease Qualifier
    Disease
    Annotation details
    Evidence
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