About   Help   FAQ
Myh4arl
Chemically induced Allele Detail
Summary
Symbol: Myh4arl
Name: myosin, heavy polypeptide 4, skeletal muscle; ariel
MGI ID: MGI:4839531
Synonyms: Myh4L342Q
Gene: Myh4  Location: Chr11:67128855-67151272 bp, + strand  Genetic Position: Chr11, 40.59 cM
Alliance: Myh4arl page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsThe mutation has been identified as a T to A transversion that is predicted to result in replacement of leucine by glutamine at amino acid position 342 of the myosin IIb (MYH4) motor domain (L342Q). (J:181892)
Inheritance:    Not Specified
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 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 Myh4 Mutation:  94 strains or lines available
References
Original:  J:181892 Kurapati R, et al., Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb. Hum Mol Genet. 2012 Apr 15;21(8):1706-24
All:  2 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/23/2024
MGI 6.23
The Jackson Laboratory