Summary | Mutation origin | Mutation description | Recombinase activity | Find Mice (IMSR) | References

Symbol:	Fabp7tm2(cre/PGR*)Ksak
Name:	fatty acid binding protein 7, brain; targeted mutation 2, Kenji Sakimura
MGI ID:	MGI:4360725
Synonyms:	BFABP-CrePR, Fabp7tm1(crePR)Ksak, Fabp7tm2(cre/PGR)Ksak
Gene:	Fabp7  Location: Chr10:57661019-57664546 bp, + strand  Genetic Position: Chr10, 29.25 cM
Alliance:	Fabp7tm2(cre/PGR*)Ksak page

Germline Transmission:	Earliest citation of germline transmission: J:104881
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	Not Specified

Allele Type:    Targeted (Inducible, Recombinase) Inducer:    mifepristone Mutation:    Insertion   Fabp7tm2(cre/PGR*)Ksak expression driven by 1 gene Knock-in expression driven by: Organism Driver Gene Note mouse Fabp7 (MGI:101916)   Mutation details: The endogenous gene's promoter drives expression of a DNA sequence encoding a fusion protein in which Cre recombinase is joined to the ligand binding domain (LBD) of the human progesterone receptor lacking the carboxyl terminal 42 amino acids. The chimeric recombinase protein is not constitutively active; its activity is inducible by binding of the synthetic progesterone analog RU486 to the truncated progesterone LBD. (J:104881, J:122587)

Activity:	Tissue activity of this recombinase allele
Driver:	Fabp7 (mouse) Summary of all recombinase alleles driven by Fabp7. Alliance mouse Fabp7 gene page

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 Fabp7 Mutation:	16 strains or lines available

Original:	J:104881 The RIKEN BioResource Center, Information obtained from The RIKEN BioResource Center. Unpublished. 2006-2013;
All:	2 reference(s)