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Myo6twt
Chemically induced Allele Detail
Summary
Symbol: Myo6twt
Name: myosin VI; twist
MGI ID: MGI:3708361
Gene: Myo6  Location: Chr9:80072313-80219011 bp, + strand  Genetic Position: Chr9, 43.98 cM
Alliance: Myo6twt page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsA point mutation introduces a T-to-A transversion replacing a tyrosine residue with a stop codon that truncates the tail domain. (J:119820)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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:119820 Schwander M, et al., A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function. J Neurosci. 2007 Feb 28;27(9):2163-75
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