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Allele : Myo10<tm1d(KOMP)Wtsi> myosin X; targeted mutation 1d, Wellcome Trust Sanger Institute

Primary Identifier  MGI:6115841 Allele Type  Targeted
Attribute String  Null/knockout Gene  Myo10
Transmission  Germline Strain of Origin  C57BL/6N-A<tm1Brd>
Is Recombinase  false Is Wild Type  false
Project Collection  KOMP-CSD
molecularNote  The L1L2_Bact_P cassette was inserted at position 25785401 of Chromosome 15 upstream of the critical exon (exon 27) (Build GRCm39). The cassette is composed of an FRT site followed by lacZ sequence and a loxP site. This first loxP site is followed by neomycin resistance gene under the control of the human beta-actin promoter, SV40 polyA, a second FRT site and a second loxP site. A third loxP site is inserted downstream of exon 27 at position 25786400. Exon 27 is thus flanked by loxP sites. A null/knockout allele was created by flp and cre recombinase expression in mice carrying this allele to remove the lacZ sequence, neo selection cassette and the loxP-flanked exon 27. Immunoblots of whole brain from P5 pups confirmed that expression of both the full-length and headless forms is undetectable in homozygous mutant mice.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • Myo10<tm1d>,
  • Myo10<tm1d>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

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6 Publication categories

Trail: Allele