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Flnbskm2
Chemically induced Allele Detail
Summary
Symbol: Flnbskm2
Name: filamin, beta; skeletal morphology mutant 2
MGI ID: MGI:5620888
Gene: Flnb  Location: Chr14:14518185-14651816 bp, - strand  Genetic Position: Chr14, 4.59 cM
Alliance: Flnbskm2 page
Mutation
origin
Strain of Origin:  129S1/SvImJ
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a T to C transition that results in the amino acid substitution of proline for serine at position 96 (S96P). (J:218364)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 5 anatomical structure(s)
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 Flnb Mutation:  151 strains or lines available
References
Original:  J:218364 Dauphinee SM, et al., Characterization of two ENU-induced mutations affecting mouse skeletal morphology. G3 (Bethesda). 2013 Oct;3(10):1753-8
All:  1 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
04/23/2024
MGI 6.23
The Jackson Laboratory