About   Help   FAQ
Myh14tm2Rsad
Targeted Allele Detail
Summary
Symbol: Myh14tm2Rsad
Name: myosin, heavy polypeptide 14; targeted mutation 2, Robert S Adelstein
MGI ID: MGI:4948885
Synonyms: 2CR722C
Gene: Myh14  Location: Chr7:44255227-44320267 bp, - strand  Genetic Position: Chr7, 28.85 cM, cytoband B2
Alliance: Myh14tm2Rsad page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:171110
Parent Cell Line:  CMT-1 (ES Cell)
Strain of Origin:  129S6/SvEvTac
Mutation
description
Allele Type:    Targeted
Mutations:    Insertion, Single point mutation
 
Mutation detailsThe targeting vector was designed to change arginine to cysteine at amino acid position 722 (R722C) by substituting CGC for TGC in exon 17. A loxP-flanked pGK neomycin cassette was also inserted in the intron. Cre mediated recombination removed the neo cassette. (J:171110)
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
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 Myh14 Mutation:  82 strains or lines available
References
Original:  J:171110 Adelstein RS, Generation of a Myh14 knockin with an R722C substitution. MGI Direct Data Submission. 2011;
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory