				Excel File Text File All mouse models of holoprosencephaly with phenotypic similarity to the human disease
				Disease Term	Allelic Composition	Genetic Background	Reference	Phenotypes
				holoprosencephaly 2	Six3tm1Gco/Six3tm1Gco	involves: 129S1/Sv	J:81797	View
				holoprosencephaly 2	Six3tm3.1Gco/Six3+ Shhtm1Chg/Shh+	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	J:140315	View
				holoprosencephaly 2	Six3tm3Gco/Six3tm3Gco Foxg1tm1(cre)Skm/Foxg1+	involves: 129S1/Sv * C57BL/6	J:140315	View
				holoprosencephaly 2	Six3tm4(cre/ERT2)Gco/Six3+	involves: 129S1/Sv * C57BL/6	J:140315	View
				holoprosencephaly 3	Disp1icb/Disp1tm1Amc Shhtm1Amc/Shh+	involves: 129X1/SvJ * C57BL/6J	J:92058	View
				holoprosencephaly 3	Shhtm1Chg/Shhtm1Chg	involves: 129S1/Sv * 129X1/SvJ	J:35802	View
				holoprosencephaly 3	Shhtm1Chg/Shhtm1Chg	involves: C57BL/6	J:89364	View
				holoprosencephaly 5	Zic2Ku/Zic2Ku	129S.CAnNCrl(C3)-Zic2^Ku	J:238567	View
				holoprosencephaly 5	Zic2Ku/Zic2Ku	C3.CAnNCrl-Zic2^Ku	J:138862	View
				holoprosencephaly 5	Zic2tm1Jaru/Zic2tm1Jaru	involves: 129S4/SvJae * C57BL/6	J:60644	View
				holoprosencephaly 11	Boctm1Rsk/Boc+ Cdontm1Rsk/Cdontm1Rsk	involves: 129/Sv * 129S6/SvEvTac	J:171767	View
				holoprosencephaly 11	Boctm1Rsk/Boctm1Rsk Cdontm1Rsk/Cdontm1Rsk	B6.129-Boc^tm1Rsk Cdon^tm1Rsk	J:171767	View
				holoprosencephaly 11	Boctm1Rsk/Boctm1Rsk Cdontm1Rsk/Cdontm1Rsk	involves: 129/Sv * 129S6/SvEvTac	J:171767	View
				holoprosencephaly 11	Boctm2Rsk/Boc+ Cdontm1Rsk/Cdontm1Rsk	involves: 129/Sv * 129S6/SvEvTac	J:171767	View
				holoprosencephaly 11	Boctm2Rsk/Boctm2Rsk Cdontm1Rsk/Cdontm1Rsk	B6.129-Boc^tm2Rsk Cdon^tm1Rsk	J:171767	View
				holoprosencephaly 11	Boctm2Rsk/Boctm2Rsk Cdontm1Rsk/Cdontm1Rsk	involves: 129/Sv * 129S6/SvEvTac	J:171767	View
				holoprosencephaly 11	Cdontm1Rsk/Cdontm1Rsk	involves: 129/Sv * C57BL/6	J:82221	View
				holoprosencephaly 11	Cdontm2Rsk/Cdontm2Rsk	involves: 129/Sv * C57BL/6	J:82221	View
				chromosome 1q41-q42 deletion syndrome	Trp53bp2tm1Xlu/Trp53bp2tm1Xlu	B6.129S6-Trp53bp2^tm1Xlu	J:240594	View
				chromosome 1q41-q42 deletion syndrome	Trp53bp2tm1Xlu/Trp53bp2tm1Xlu	C.129S6-Trp53bp2^tm1Xlu	J:240594	View
				chromosome 1q41-q42 deletion syndrome	Trp53bp2tm1Xlu/Trp53bp2tm1Xlu	involves: 129S6/SvEvTac * C57BL/6J	J:240594	View
				holoprosencephaly	NosipGt(OST138992)Lex/NosipGt(OST138992)Lex	B6.129S5-Nosip^{Gt(OST138992)Lex}	J:245546	View
				holoprosencephaly	Pgap1m1Nisw/Pgap1m1Nisw	involves: C57BL/6J	J:187360	View
				holoprosencephaly	Pignm1Nisw/Pignm1Nisw	involves: 129S1/SvImJ * C3H/HeJ * C57BL/6J	J:187360	View
Additional Complex Models				holoprosencephaly	Chrdtm1Emdr/Chrdtm1Emdr Nodaltm1Rob/Nodal+	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ	J:161524	View
Additional Complex Models				holoprosencephaly	Nogtm1Amc/Nogtm1Amc Smad3tm1Xfw/Smad3+	involves: 129/Sv * 129S1/Sv	J:161524	View

				No similarity to the expected human disease phenotype was found.
				Disease Term	Allelic Composition	Genetic Background	Reference	Phenotypes
NOT Models				holoprosencephaly 4	Tgif1tm1.1Caw/Tgif1tm1.1Caw	involves: C57BL/6 * FVB/N	J:97642	View