About   Help   FAQ
Myh10tm3.1Rsad
Targeted Allele Detail
Summary
Symbol: Myh10tm3.1Rsad
Name: myosin, heavy polypeptide 10, non-muscle; targeted mutation 3.1, Robert S Adelstein
MGI ID: MGI:3052112
Synonyms: 2BR709C, BC, BR709C
Gene: Myh10  Location: Chr11:68582385-68707458 bp, + strand  Genetic Position: Chr11, 41.95 cM, cytoband B3
Alliance: Myh10tm3.1Rsad page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:92081
Parent Cell Line:  CMT-1 (ES Cell)
Strain of Origin:  129S6/SvEvTac
Mutation
description
Allele Type:    Targeted (Humanized sequence)
Mutation:    Nucleotide substitutions
 
Mutation detailsCrossing Myh10tm3Rsad mice with mice expressing cre in the germ line created this allele in which the floxed neo is excised, leaving a single loxP site upstream of exon 17 and the R709C mutation in exon 17. Western blot indicates the allele expression in mutant brains is restored to wild-type levels. (J:92081)
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 11 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Myh10 Mutation:  95 strains or lines available
References
Original:  J:92081 Ma X, et al., A point mutation in the motor domain of nonmuscle myosin II-B impairs migration of distinct groups of neurons. Mol Biol Cell. 2004 Jun;15(6):2568-79
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
04/16/2024
MGI 6.23
The Jackson Laboratory