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Myo6Tur
Chemically induced Allele Detail
Summary
Symbol: Myo6Tur
Name: myosin VI; Turner
MGI ID: MGI:5882958
Synonyms: Tur
Gene: Myo6  Location: Chr9:80072313-80219011 bp, + strand  Genetic Position: Chr9, 43.98 cM
Alliance: Myo6Tur page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsENU treatment induced a 820A to T mutation in exon 8, resulting in an Asn200Ile substitution in the peptide encoded by this allele. This substitution affects an extremely well-conserved amino-acid residue. (J:240216)
Inheritance:    Dominant
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
Notes
Generated in a large-scale ENU mutagenesis project at the McLaughlin Research Institute.
References
Original:  J:240216 Wong EY, et al., A Novel ENU-Induced Mutation in Myo6 Causes Vestibular Dysfunction and Deafness. PLoS One. 2016;11(5):e0154984
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
06/12/2024
MGI 6.13
The Jackson Laboratory