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

Symbol:	Sox4tm1.1Vlf
Name:	SRY (sex determining region Y)-box 4; targeted mutation 1.1, Veronique Lefebvre
MGI ID:	MGI:3773013
Synonyms:	Sox4fl-
Gene:	Sox4  Location: Chr13:29132902-29137682 bp, - strand  Genetic Position: Chr13, 12.87 cM, cytoband A3-A5
Alliance:	Sox4tm1.1Vlf page

Germline Transmission:	Earliest citation of germline transmission: J:130461
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: The coding region of the gene was removed by germ-line, cre-mediated recombination. The absence of absence of transcript was confirmed by northern blot analysis on total RNA from E12.5 embryos. (J:130461)

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

In Mice Carrying this Mutation:	2 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 Sox4 Mutation:	20 strains or lines available

Original:	J:130461 Penzo-Mendez A, et al., Generation of mice harboring a Sox4 conditional null allele. Genesis. 2007 Dec;45(12):776-80
All:	3 reference(s)