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

Symbol:	Tsc22d3tm1.1Ric
Name:	TSC22 domain family, member 3; targeted mutation 1.1, Carlo Riccardi
MGI ID:	MGI:5308358
Synonyms:	Gilz KO
Gene:	Tsc22d3  Location: ChrX:139440277-139501257 bp, - strand  Genetic Position: ChrX, 61.35 cM, cytoband F1
Alliance:	Tsc22d3tm1.1Ric page

Germline Transmission:	Earliest citation of germline transmission: J:179667
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	C57BL/6

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: One loxP site was inserted upstream of exon 6 and a second loxP was placed downstream. An FRT flanked neomycin cassette was located further downstream. Exon 6 was then excised in properly targeted mice. (J:179667)

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

In Structures Affected by this Mutation:

2 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 Tsc22d3 Mutation:	5 strains or lines available

Original:	J:179667 Bruscoli S, et al., Long Glucocorticoid-induced Leucine Zipper (L-GILZ) Protein Interacts with Ras Protein Pathway and Contributes to Spermatogenesis Control. J Biol Chem. 2012 Jan 6;287(2):1242-51
All:	5 reference(s)