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Allele : Myh9<tm1.1(MYH9*)Mjk> myosin, heavy polypeptide 9, non-muscle; targeted mutation 1.1, Michael J Kelley

Primary Identifier  MGI:5285646 Allele Type  Targeted
Attribute String  Humanized sequence Gene  Myh9
Inheritance Mode  Semidominant Transmission  Germline
Strain of Origin  (129X1/SvJ x 129S1/Sv)F1-Kitl<+> Is Recombinase  false
Is Wild Type  false
molecularNote  The endogenous myosin, heavy polypeptide 9, non-muscle (Myh9) gene was modified by the introduction into exon 39 of a mutation resulting in replacement of glutamic acid with lysine at amino acid position 1841, in the rod region of the protein (E1841K), and by insertion of a loxP-flanked PGK-neor cassette into the preceding intron (intron 38). This modification replicates a mutation associated with a human MYH9-related disease (MYH9-RD). The selection cassette has been deleted by Cre recombinase-mediated excision. Immunoblot analysis demonstrates that levels of MYH9 protein are similar in lungs of homozygous mutant, heterozygous and wild-type mice.
  • mutations:
  • Single point mutation
  • synonyms:
  • NMHCII-A E1841K,
  • A<E1841K>,
  • A<E1841K>,
  • NMHCII-A E1841K
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

3 Carried By

Trail: Allele

0 Driven By

7 Publication categories

Trail: Allele