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

Symbol:	Sox6tm2.2Vlf
Name:	SRY (sex determining region Y)-box 6; targeted mutation 2.2, Veronique Lefebvre
MGI ID:	MGI:3641205
Synonyms:	Sox6fl-
Gene:	Sox6  Location: Chr7:115070107-115638031 bp, - strand  Genetic Position: Chr7, 61.29 cM
Alliance:	Sox6tm2.2Vlf page

Germline Transmission:	Earliest citation of germline transmission: J:110147
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	129/Sv

Allele Type:    Targeted (Null/knockout) Mutation:    Intragenic deletion   Mutation details: Exon 2 was flanked by a single loxP site and an frt flanked neo followed by a single loxP site. Cre mediated recombination then removed exon 2 and the neo cassette (J:110147)

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

In Mice Carrying this Mutation:	6 assay results
In Structures Affected by this Mutation:	1 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 Sox6 Mutation:	59 strains or lines available

Original:	J:110147 Dumitriu B, et al., Generation of mice harboring a Sox6 conditional null allele. Genesis. 2006 May;44(5):219-24
All:	4 reference(s)