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Flnatm1.1Caw
Targeted Allele Detail
Summary
Symbol: Flnatm1.1Caw
Name: filamin, alpha; targeted mutation 1.1, Christopher A Walsh
MGI ID: MGI:3699305
Synonyms: Flnac, FlnAloxP
Gene: Flna  Location: ChrX:73267067-73293426 bp, - strand  Genetic Position: ChrX, 37.89 cM
Alliance: Flnatm1.1Caw page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:118252
Parent Cell Line:  J1 (ES Cell)
Strain of Origin:  129S4/SvJae
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsA combination of homologous recombination and transient cre expression resulted in the flanking of exons 3-7 with loxP sites. (J:118252)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 7 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 Flna Mutation:  19 strains or lines available
References
Original:  J:118252 Feng Y, et al., Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis. Proc Natl Acad Sci U S A. 2006 Dec 26;103(52):19836-41
All:  25 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
12/10/2024
MGI 6.24
The Jackson Laboratory