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Allele : Tyro3<m1> TYRO3 protein tyrosine kinase 3; mutation 1
Primary Identifier  MGI:6197245 Allele Type  Spontaneous
Gene  Tyro3 Inheritance Mode  Recessive
Strain of Origin  various Is Recombinase  false
Is Wild Type  false
molecularNote  A single C-to-T transition in the signal sequence causes an arginine to tryptophan substitution at amino acid 13 (p.R13W).
  • mutations:
  • Single point mutation
  • synonyms:
  • Tyro3<R7Y>,
  • Tyro3<R7Y>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

4 Carried By

0 Driven By

4 Publication categories





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