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Myo6chl
Chemically induced Allele Detail
Summary
Symbol: Myo6chl
Name: myosin VI; charlie
MGI ID: MGI:5449854
Gene: Myo6  Location: Chr9:80072313-80219011 bp, + strand  Genetic Position: Chr9, 43.98 cM
Alliance: Myo6chl page
Mutation
origin
Strain of Origin:  C57BL/6JAnu
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a G to A intronic point mutation 5 bp downstream of exon 5 that results in skipping of exon 5 and the introduction of a stop codon at position 95 of 1262 amino acids. QRT-PCR confirmed the absence of transcript expression in the brain.
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Myo6 Mutation:  90 strains or lines available
References
Original:  J:196601 Williams LH, et al., Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction. Hear Res. 2013 May;299:53-62
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory