Gene Expression Literature Summary

• Symbol: Gtf2ird2
• Name: GTF2I repeat domain containing 2
• ID: MGI:2149780

3 matching records from 3 references.

Summary by Age and Assay: Numbers in the table indicate the number of results matching the search criteria.

Age	E12.5	E13.5	E14.5	E15.5	P
In situ RNA (section)	1	1	1		1
In situ RNA (whole mount)				1
RT-PCR					1

Summary by Gene and Reference: Number indicates the number of results matching the search criteria recorded for each reference.
* Indicates detailed expression data entries available

Gtf2ird2  GTF2I repeat domain containing 2   (Synonyms: 1700012P16Rik)
Results	Reference
1*	J:171409 GUDMAP Consortium, GUDMAP: the GenitoUrinary Development Molecular Anatomy Project. www.gudmap.org. 2004;
4*	J:125494 Ohazama A, Sharpe PT, TFII-I gene family during tooth development: Candidate genes for tooth anomalies in Williams syndrome. Dev Dyn. 2007 Oct;236(10):2884-8
1	J:285870 Sakurai T, Dorr NP, Takahashi N, McInnes LA, Elder GA, Buxbaum JD, Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions. Autism Res. 2011 Feb;4(1):28-39