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

Symbol:	Fn1tm3Hyn
Name:	fibronectin 1; targeted mutation 3, Richard Hynes
MGI ID:	MGI:2177826
Synonyms:	FNB2, FN.B2
Gene:	Fn1  Location: Chr1:71624679-71692359 bp, - strand  Genetic Position: Chr1, 36.05 cM, cytoband C1-C5
Alliance:	Fn1tm3Hyn page

Germline Transmission:	Earliest citation of germline transmission: J:36210
Parent Cell Line:	D3 (ES Cell)
Strain of Origin:	129S2/SvPas

Allele Type:    Targeted (Inserted expressed sequence, Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: A partial cDNA fragment corresponding to sequences of exons III7b, EIIIB and III8a replaced the genomic fragment containing these three exons. The encoded protein was not detectable in immunoprecipitations from cultures of homozygous mutant E7.5 embryos. (J:36210)

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 Fn1 Mutation:	129 strains or lines available

Original:	J:36210 Georges-Labouesse EN, et al., Mesodermal development in mouse embryos mutant for fibronectin. Dev Dyn. 1996 Oct;207(2):145-56
All:	1 reference(s)