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

Symbol:	Gtf2ird1tm2Hrd
Name:	general transcription factor II I repeat domain-containing 1; targeted mutation 2, Edna C Hardeman
MGI ID:	MGI:3698407
Synonyms:	Gtf2ird1tm2(lacZ)Hrd
Gene:	Gtf2ird1  Location: Chr5:134386510-134485570 bp, - strand  Genetic Position: Chr5, 74.55 cM
Alliance:	Gtf2ird1tm2Hrd page

Germline Transmission:	Earliest citation of germline transmission: J:117884
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	129

Allele Type:    Targeted Mutation:    Insertion   Mutation details: The insertion of a lacZ-floxed neo interrupted exon 2 at the ATG. The neo was subsequently removed via cre-mediated recombination. (J:117884)

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

In Mice Carrying this Mutation:

259 assay results

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 Gtf2ird1 Mutation:	358 strains or lines available

Original:	J:117884 Palmer SJ, et al., Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development. Gene Expr Patterns. 2007 Feb;7(4):396-404
All:	3 reference(s)