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Allele : Atmin<m1H> ATM interactor; mutation 1, Harwell

Primary Identifier  MGI:5620361 Allele Type  Chemically induced (ENU)
Gene  Atmin Inheritance Mode  Recessive
Strain of Origin  BALB/c Is Recombinase  false
Is Wild Type  false
molecularNote  ENU mutagenesis induced a point mutation that results in the amino acid substitution of glutamine for histidine at position 210 (H210Q) in the fourth zinc finger. This mutation is predicted to interfer with zinc chelation.
  • mutations:
  • Single point mutation
  • synonyms:
  • Atmin<H210Q>,
  • Atmin<H210Q>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

Trail: Allele

0 Driven By

4 Publication categories

Trail: Allele