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Allele : Myo7a<4626SB> myosin VIIA; shaker 4626SB

Primary Identifier  MGI:2155422 Allele Type  Chemically induced (ENU)
Gene  Myo7a Inheritance Mode  Recessive
Strain of Origin  BALB/cRl Is Recombinase  false
Is Wild Type  false
molecularNote  A C-to-T transition mutation is predicted to result in a glutamine to stop codon change at position 720 in the encoded protein. This mutation is predicted to lie within the head domain of the protein. Northern blot analysis indicated that mRNA expression, size, and stability were unaffected. Immunoblot analysis showed that less than 1% of the normal level of the protein was expressed.
  • mutations:
  • Single point mutation
  • synonyms:
  • sh1<4626SB>,
  • sh1<OR-4626SB>,
  • sh1<4626SB>,
  • shaker-1,
  • shaker-1,
  • Myo7a<sh1-5R>,
  • sh1<OR-4626SB>,
  • Myo7a<sh1-5R>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

Trail: Allele

0 Driven By

26 Publication categories

Trail: Allele