Saa3^l7R3-2R
Chemically induced Allele Detail

Summary

• Symbol: Saa3^l7R3-2R
• Name: serum amyloid A 3; 2 Oak Ridge
• MGI ID: MGI:2449592
• Synonyms: 951SJ
• Gene: Saa3 Location: Chr7:46361422-46365100 bp, - strand Genetic Position: Chr7, 30.51 cM
• Alliance: Saa3^l7R3-2R page

Mutation origin

• Strain of Origin: BJR

Mutation description

• Allele Type: Chemically induced (ENU)
• Mutation: Single point mutation
• Mutation details: 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). (J:101682)
• Inheritance: Recessive

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 0 strains available Cell Lines: 0 lines available
• Carrying any Saa3 Mutation: 19 strains or lines available

References

• Original: J:73982 Rinchik EM, et al., Functional annotation of mammalian genomic DNA sequence by chemical mutagenesis: A fine-structure genetic mutation map of a 1- to 2-cM segment of mouse chromosome 7 corresponding to human chromosome 11p14-p15. Proc Natl Acad Sci U S A. 2002 Jan 22;99(2):844-9
• All: 2 reference(s)