Fth1^Fer001
Chemically induced Allele Detail

Summary

• Symbol: Fth1^Fer001
• Name: ferritin heavy polypeptide 1; abnormal ferritin level 001
• MGI ID: MGI:6120532
• Synonyms: Fth1^S32P
• Gene: Fth1 Location: Chr19:9957962-9962462 bp, + strand Genetic Position: Chr19, 6.23 cM, cytoband A-C
• Alliance: Fth1^Fer001 page

Mutation origin

• Strain of Origin: C3HeB/FeJ

Mutation description

• Allele Type: Chemically induced (ENU) (Not Specified)
• Mutation: Single point mutation
• Mutation details: ENU induced a T to C point mutation at nucleotide 97 of the coding sequence resulting In a serine to proline mutation at position 32. (J:256080)
• Inheritance: Dominant

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 Fth1 Mutation: 13 strains or lines available

References

• Original: J:256080 Rathkolb B, et al., Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levels. Biometals. 2015 Apr;28(2):293-306
• All: 1 reference(s)