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Myh1tm1Lnwd
Targeted Allele Detail
Summary
Symbol: Myh1tm1Lnwd
Name: myosin, heavy polypeptide 1, skeletal muscle, adult; targeted mutation 1, Leslie A Leinwand
MGI ID: MGI:2183827
Synonyms: IId/x-
Gene: Myh1  Location: Chr11:67090922-67115401 bp, + strand  Genetic Position: Chr11, 40.59 cM
Alliance: Myh1tm1Lnwd page
Myh1tm1Lnwd/Myh1tm1Lnwd mice exhibit kyphosis

Show the 2 phenotype image(s) involving this allele.

Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:44448
Parent Cell Line:  E14.1 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Insertion
 
Mutation detailsExon 3, which is the first coding exon, was disrupted by the insertion of a neomycin selection cassette. RNAse protection assays of various tissues showed an absence of transcript in homozygous mutant mice. The lack of protein was confirmed by high resolution gel electrophoresis of tongue tissue. (J:44448)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 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 Myh1 Mutation:  109 strains or lines available
References
Original:  J:44448 Acakpo-Satchivi LJ, et al., Growth and muscle defects in mice lacking adult myosin heavy chain genes. J Cell Biol. 1997 Dec 1;139(5):1219-29
All:  4 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
04/23/2024
MGI 6.23
The Jackson Laboratory