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Allele : Mypn<em1(IMPC)J> myopalladin; endonuclease-mediated mutation 1, Jackson

Primary Identifier  MGI:6149973 Allele Type  Endonuclease-mediated
Attribute String  Null/knockout Gene  Mypn
Inheritance Mode  Not Specified Strain of Origin  C57BL/6NJ
Is Recombinase  false Is Wild Type  false
Project Collection  IMPC
molecularNote  This allele was generated at The Jackson Laboratory by injecting Cas9 RNA and 4 guide sequences CCATTATAACGGGAATTCAT, AGTTACGTAAACATTTGTAG, CAGAATGCGAAGTAAACCTT and GCTTGTATGTAGGTCTCCTC, which resulted in a 579 bp deletion beginning at Chromosome 10 position 63,169,099 bp and ending after 63,169,677 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000420052 (exon 3) and 403 bp of flanking intronic sequence including the splice acceptor and donor. In addition, there is a 9 bp insertion (TGCCTTGGT) at the deletion site and a single bp insertion (A) 38 bp after the exon deletion that will not alter the results of the exon deletion. This mutation is predicted to cause a change of amino acid sequence after residue 299 and early truncation 4 amino acids later.
  • mutations:
  • Intragenic deletion
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

4 Publication categories

Trail: Allele