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

Symbol:	Foxf1tm1Rhc
Name:	forkhead box F1; targeted mutation 1, Robert H Costa
MGI ID:	MGI:2179135
Synonyms:	Foxf1-
Gene:	Foxf1  Location: Chr8:121811125-121814883 bp, + strand  Genetic Position: Chr8, 70.31 cM, cytoband E1
Alliance:	Foxf1tm1Rhc page

Germline Transmission:	Earliest citation of germline transmission: J:70364
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	Not Specified

Allele Type:    Targeted (Null/knockout, Reporter) Mutations:    Insertion, Intragenic deletion   Mutation details: The genomic sequences encoding the N-terminal winged-helix DNA binding domain are replaced with a cassette containing a LacZ gene with a nuclear localization sequence and a PGK/neo gene. (J:70364)

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

In Mice Carrying this Mutation:	68 assay results
In Structures Affected by this Mutation:	4 anatomical structure(s)

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 Foxf1 Mutation:	13 strains or lines available

Original:	J:70364 Kalinichenko VV, et al., Defects in pulmonary vasculature and perinatal lung hemorrhage in mice heterozygous null for the Forkhead Box f1 transcription factor. Dev Biol. 2001 Jul 15;235(2):489-506
All:	11 reference(s)