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Allele : Saa3<l7R3-2R> serum amyloid A 3; 2 Oak Ridge

Primary Identifier  MGI:2449592 Allele Type  Chemically induced (ENU)
Gene  Saa3 Inheritance Mode  Recessive
Strain of Origin  BJR Is Recombinase  false
Is Wild Type  false
molecularNote  This phenotypic mutant was identified in an ENU mutagenesis screen at The Oak Ridge National Laboratory. A C-to-T mutation results in a serine to phenylalanine substitution at codon 40 (S40F).
  • mutations:
  • Single point mutation
  • synonyms:
  • 951SJ,
  • 951SJ
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

3 Publication categories

Trail: Allele