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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
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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:  3 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