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Allele : Myh11<tm1.1Dmmz> myosin, heavy polypeptide 11, smooth muscle; targeted mutation 1.1, Dianna M Milewicz

Primary Identifier  MGI:5582321 Allele Type  Targeted
Attribute String  Not Specified Gene  Myh11
Transmission  Germline Strain of Origin  129S/SvEv
Is Recombinase  false Is Wild Type  false
molecularNote  A loxP site was inserted upstream of a modified exon 7 in which a C to T point mutation results in the amino acid substitution of cysteine for arginine at position 247 (R247C). This mutation mimics a rare variant identified in humans. Flp-mediated recombination removed an FRT flanked neomycin resistance cassette inserted downstream of exon 8, leaving single loxP and FRT sites.
  • mutations:
  • Single point mutation,
  • Insertion
  • synonyms:
  • Myh11<R247C>,
  • Myh11<R247C>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

7 Publication categories