Excel File Text File All mouse models of Williams-Beuren syndrome with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      Williams-Beuren syndrome Del(5Gtf2i-Fkbp6)1Vcam/+ B6.129-Del(5Gtf2i-Fkbp6)1Vcam(J:204278) J:216195 View
Williams-Beuren syndrome Del(5Gtf2i-Limk1)1Uta/Del(5Limk1-Trim50)2Uta involves: 129S7/SvEvBrd * C57BL/6J J:182796 View
Williams-Beuren syndrome Eif4hGt(Ex279)Byg/Eif4hGt(Ex279)Byg involves: 129P2/OlaHsd * C57BL/6 J:181945 View
      Williams-Beuren syndrome b2b370Clo/b2b370Clo C57BL/6J-b2b370Clo J:175213 View
Williams-Beuren syndrome Baz1bMommeD10/Baz1b+ involves: FVB/N J:142335 View
Williams-Beuren syndrome Baz1bMommeD10/Baz1bMommeD10 involves: FVB/N J:142335 View
Williams-Beuren syndrome Baz1btm1Ska/Baz1b+ involves: C57BL/6 * CBA J:149990 View
Williams-Beuren syndrome Baz1btm1Ska/Baz1btm1Ska involves: C57BL/6 * CBA J:149990 View
Williams-Beuren syndrome Clip2tm1.1Gal/Clip2+ involves: 129P2/OlaHsd * C57BL/6 J:78711 View
Williams-Beuren syndrome Dlg4tm2.1Grnt/Dlg4tm2.1Grnt involves: 129P2/OlaHsd * C57BL/6J J:175436 View
Williams-Beuren syndrome Fzd9tm1Sjp/Fzd9tm1Sjp involves: C57BL/6J J:99893 View
Williams-Beuren syndrome Fzd9tm1Uta/Fzd9+ involves: 129X1/SvJ J:169924 View
Williams-Beuren syndrome Gtf2iGt(XE029)Byg/Gtf2i+ involves: 129P2/OlaHsd * C57BL/6 J:143508 View
Williams-Beuren syndrome Gtf2itm1Vcam/Gtf2itm1Vcam involves: 129S1/Sv * 129X1/SvJ * CD-1 J:204278 View
Williams-Beuren syndrome Gtf2ird1Gt(XE465)Byg/Gtf2ird1+ involves: 129P2/OlaHsd * C57BL/6 J:143508 View
Williams-Beuren syndrome Gtf2ird1Tg(Alb1-Myc)166.8Sst/Gtf2ird1Tg(Alb1-Myc)166.8Sst involves: C57BL/6 * CBA J:102709 View
Williams-Beuren syndrome Gtf2ird1Tg(Alb1-Myc)166.8Sst/Gtf2ird1Tg(Alb1-Myc)166.8Sst involves: C57BL/6J * CBA/J J:190478 View
Williams-Beuren syndrome Gtf2ird1tm1Hrd/Gtf2ird1tm1Hrd involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:182346 View
Williams-Beuren syndrome Limk1tm1Zpj/Limk1tm1Zpj involves: 129 J:86283 View
Williams-Beuren syndrome Loxb2b370.2Clo/Loxb2b370.2Clo C57BL/6J-Loxb2b370.2Clo J:175213 View
Williams-Beuren syndrome Srcinl/Srcinl involves: 129 J:229610 View

       
No similarity to the expected human disease phenotype was found.
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
NOT Models      Williams-Beuren syndrome Fzd9tm1Uta/Fzd9tm1Uta involves: 129S6/SvEvTac * 129X1/SvJ J:98133 View