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

Symbol:	Foxi1tm1Sven
Name:	forkhead box I1; targeted mutation 1, Sven Enerback
MGI ID:	MGI:2448634
Synonyms:	Fkh10-
Gene:	Foxi1  Location: Chr11:34154341-34158089 bp, - strand  Genetic Position: Chr11, 19.65 cM, cytoband A5
Alliance:	Foxi1tm1Sven page

Germline Transmission:	Earliest citation of germline transmission: J:51291
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: The gene was disrupted by replacement of the forkhead domain-encoding exon with a PGK-neo cassette via homologous recombination. (J:51291)

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

In Structures Affected by this Mutation:

17 anatomical structure(s)

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 Foxi1 Mutation:	17 strains or lines available

Original:	J:51291 Hulander M, et al., The winged helix transcription factor Fkh10 is required for normal development of the inner ear. Nat Genet. 1998 Dec;20(4):374-6
All:	9 reference(s)