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Allele : Amelx<Rgsc888> amelogenin, X-linked; RIKEN Genomic Sciences Center (GSC), 888

Primary Identifier  MGI:3807977 Allele Type  Chemically induced (ENU)
Gene  Amelx Inheritance Mode  Dominant
Strain of Origin  C57BL/6JJcl Is Recombinase  false
Is Wild Type  false Project Collection  RIKEN GSC ENU Project
molecularNote  An ENU induced T to C transition at nucleotide 249 of coding sequence resulted in the missense mutation Y64H in the encoded protein. RT-PCR showed no differences in the mRNA level. SDS-PAGE of secretory stage developing enamel showed lack of high molecular weight nascent amelogenin proteins in hemizygous males.
  • mutations:
  • Single point mutation
  • synonyms:
  • Amelx<Y64H>,
  • M100888,
  • Amelx<Y64H>,
  • M100888
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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

6 Publication categories

Trail: Allele