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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
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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)
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last database update
10/22/2024
MGI 6.24
The Jackson Laboratory