Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	Fbxl21Psttm
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:	Fbxl21Psttm page

Strain of Origin:

C57BL/6J

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

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

1 anatomical structure(s)

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:	25 strains or lines available

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:	3 reference(s)