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Fbxl3Ovtm
Chemically induced Allele Detail
Nomenclature
Symbol: Fbxl3Ovtm
Name: F-box and leucine-rich repeat protein 3; overtime
MGI ID: MGI:2449078
Gene: Fbxl3  Location: Chr14:103080239-103099566 bp, - strand  Genetic Position: Chr14, 51.73 cM, cytoband E2.2
Mutation
origin
Strain of Origin:  BTBR T+ Itpr3tf/J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsThis phenotypic mutant was identified in an ENU mutagenesis screen. Subsequently, a single A to G transition was identified in exon 5. This results in the conversion of amino acid residue 364 from isoleucine to threonine. (J:122872)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Fbxl3 Mutation:  19 strains or lines available
References
Original:  J:83419 Center for Functional Genomics (CFG) at Northwestern University, Heritable mouse mutants from Neurogenomics Project at Northwestern University. MGI Direct Data Submission. 2003;
All:  4 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
04/13/2021
MGI 6.16
The Jackson Laboratory