Fbxl21^Psttm
Chemically induced Allele Detail

Summary

• Symbol: Fbxl21^Psttm
• Name: F-box and leucine-rich repeat protein 21; past-time
• MGI ID: MGI:3522308
• Synonyms: Psttm
• Gene: Fbxl21 Location: Chr13:56670285-56685711 bp, + strand Genetic Position: Chr13, 30.07 cM
• Alliance: Fbxl21^Psttm page

Mutation origin

• Strain of Origin: C57BL/6J

Mutation description

• Allele Type: Chemically induced (ENU)
• Mutation: Single point mutation
• Mutation details: ENU induced a single G to A change at nucleotide 787 in exon 5 resulting in a glycine to a glutamic acid mutation in amino acid 149 within the third leucine-rich repeat of the protein. (J:194037)
• Inheritance: Semidominant

Expression

In Structures Affected by this Mutation:

1 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 1 strain available Cell Lines: 0 lines available
• Carrying any Fbxl21 Mutation: 26 strains or lines available

References

• Original: J:91116 Center for Functional Genomics (CFG) at Northwestern University, Heritable mouse mutants from Neurogenomics Project at Northwestern University. MGI Direct Data Submission. 2004-5
• All: 4 reference(s)