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

Symbol:	Fblim1tm1.2Ref
Name:	filamin binding LIM protein 1; targeted mutation 1.2, Reinhard Fassler
MGI ID:	MGI:5317180
Synonyms:	migfillin-
Gene:	Fblim1  Location: Chr4:141303373-141333351 bp, - strand  Genetic Position: Chr4, 74.64 cM, cytoband E1
Alliance:	Fblim1tm1.2Ref page

Germline Transmission:	Earliest citation of germline transmission: J:182886
Parent Cell Line:	R1 (ES Cell)
Strain of Origin:	(129X1/SvJ x 129S1/Sv)F1-Kitl+

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: Cre-mediated recombination of Fblim1tm1.1Ref removed exons 2 and 3. Western blot analysis confirmed the absence of protein expression in heart and lung extracts. (J:182886)

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

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 Fblim1 Mutation:	82 strains or lines available

Original:	J:182886 Moik DV, et al., Loss of migfilin expression has no overt consequences on murine development and homeostasis. J Cell Sci. 2011 Feb 1;124(Pt 3):414-21
All:	2 reference(s)