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

Symbol:	Foxh1tm1.1Hmd
Name:	forkhead box H1; targeted mutation 1.1, Hiroshi Hamada
MGI ID:	MGI:2654232
Synonyms:	Foxh1-
Gene:	Foxh1  Location: Chr15:76552425-76554148 bp, - strand  Genetic Position: Chr15, 36.24 cM
Alliance:	Foxh1tm1.1Hmd page

Germline Transmission:	Earliest citation of germline transmission: J:69593
Parent Cell Line:	R1 (ES Cell)
Strain of Origin:	(129X1/SvJ x 129S1/Sv)F1-Kitl+

Allele Type:    Targeted (Null/knockout) Mutation:    Intragenic deletion   Mutation details: This allele is derived from Foxh1tm1Hmd. Mutant animals were bred to cre-expressing line Tg(ACTB-cre)13Miya to delete exon 2 and the neo cassette. Homozygous mutant embryos did not express gene transcripts as determined by Northern blot and RT-PCR analysis. (J:69593)

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

In Mice Carrying this Mutation:	49 assay results
In Structures Affected by this Mutation:	10 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 Foxh1 Mutation:	34 strains or lines available

Original:	J:69593 Yamamoto M, et al., The transcription factor FoxH1 (FAST) mediates Nodal signaling during anterior-posterior patterning and node formation in the mouse. Genes Dev. 2001 May 15;15(10):1242-56
All:	5 reference(s)