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Allele : Enam<abte> enamelin; abnormal tooth enamel
Primary Identifier  MGI:3512772 Allele Type  Chemically induced (ENU)
Gene  Enam Inheritance Mode  Semidominant
Strain of Origin  C3HeB/FeJ Is Recombinase  false
Is Wild Type  false
molecularNote  The molecular lesion is a C-to-T substitution at position 826 of the cDNA, resulting in the introduction of a stop codon at amino acid 176 of the encoded protein.
  • mutations:
  • Single point mutation
  • synonyms:
  • ate,
  • Enam<ATE1>,
  • ate,
  • ATE1,
  • ATE1,
  • Enam<ATE1>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

5 Publication categories

Trail: Allele




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