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Allele : Tfrc<Rbc21> transferrin receptor; red blood cell mutant 21
Primary Identifier  MGI:6406257 Allele Type  Chemically induced (ENU)
Attribute String  Not Specified Gene  Tfrc
Inheritance Mode  Dominant Strain of Origin  C57BL/6
Is Recombinase  false Is Wild Type  false
molecularNote  ENU mutagenesis induced a G to a point mutation that results in the amino acid substitutin of histidine for arginine at position 654 (R654H).
  • mutations:
  • Single point mutation
  • synonyms:
  • Tfrc<R654H>,
  • Tfrc<R654H>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

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Trail: Allele




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