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Allele : Cat<b> catalase; acatalasemia

Primary Identifier  MGI:3053604 Allele Type  Radiation induced
Gene  Cat Inheritance Mode  Recessive
Strain of Origin  (101 x C3H)F1 Is Recombinase  false
Is Wild Type  false
molecularNote  This allele corresponds to a mutation located in the first alpha helix in the amino terminal arm of the catalase subunit. The substitution of G to T results in an amino acid substitution that replaces glutamine with histidine at position 11.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • M1,
  • Cs<b>,
  • M1,
  • Cs<b>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

4 Carried By

Trail: Allele

0 Driven By

22 Publication categories

Trail: Allele