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Inside the deletion region, a transcription factor<jats:italic>TBX1<\/jats:italic>was highly suspected. Furthermore, similar DGS phenotypes were found in the<jats:italic>Tbx1<\/jats:italic>heterozygous knockout mice. Using ENU-induced mutagenesis and G1 dominant screening strategy, here we identified a nonsynonymous mutation p.W118R in T-box of TBX1, the DNA binding domain for transcription activity. The mutant mice showed deficiency of inner ear functions, including head tossing and circling, plus increased hearing threshold determined by audiometry. Therefore, our result further confirms the pathogenic basis of<jats:italic>Tbx1<\/jats:italic>in DGS, points out the crucial role of DNA binding activity of TBX1 for the ear function, and provides additional animal model for studying the DGS disease mechanisms.<\/jats:p>","DOI":"10.1155\/2016\/5836143","type":"journal-article","created":{"date-parts":[[2016,12,26]],"date-time":"2016-12-26T21:21:03Z","timestamp":1482787263000},"page":"1-10","source":"Crossref","is-referenced-by-count":15,"title":["Identification of a Novel ENU-Induced Mutation in Mouse<i>Tbx1<\/i>Linked to Human DiGeorge Syndrome"],"prefix":"10.1155","volume":"2016","author":[{"given":"Jiaofeng","family":"Chen","sequence":"first","affiliation":[{"name":"School of Life Sciences, Tsinghua University, Beijing, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xue","family":"Zhang","sequence":"additional","affiliation":[{"name":"School of Medicine, Tsinghua University, Beijing, 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