Myh10^tm3Rsad

别称:

B^R709CN

B^CN

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Basic Information

Phenotypes

References Literature

An arginine to cysteine mutation at amino acid 709 was inserted in exon 17 by homologous recombination. A floxed neo was inserted into intron 15. Southern blot and PCR confirmed recombination. Western blot indicated that this is a hypomorphic allele: expression in mutant brains was reduced 73% from wild-type levels. (J:92081)

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