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Allele : Tyr<c-44H> tyrosinase; albino 44 Harwell
Primary Identifier  MGI:1856307 Allele Type  Chemically and radiation induced
Gene  Tyr Inheritance Mode  Recessive
Strain of Origin  (C3H/HeH x 101/H)F1 Is Recombinase  false
Is Wild Type  false
molecularNote  The defect is a G-to-T point mutation, altering serine to isoleucine at position 146 or 128 (p.S146I in pre-protein, p.S128I in mature protein) in the encoded protein.
  • mutations:
  • Single point mutation
  • synonyms:
  • c<44H>,
  • dark-eyed albino,
  • dark-eyed albino,
  • c<44H>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

5 Publication categories





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