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Fbxl21Psttm
Chemically induced Allele Detail
Nomenclature
Symbol: Fbxl21Psttm
Name: F-box and leucine-rich repeat protein 21; past-time
MGI ID: MGI:3522308
Synonyms: Psttm
Gene: Fbxl21  Location: Chr13:56522472-56537898 bp, + strand  Genetic Position: Chr13, 30.07 cM
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU 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
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structures
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:  6 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:  3 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
03/30/2021
MGI 6.16
The Jackson Laboratory