13 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Cer1tm1Bhr/Cer1tm1Bhr Lhx1tm1Bhr/Lhx1+ involves: 129S7/SvEvBrd * C57BL/6	no abnormal phenotype detected	J:62080
En1tm2(cre)Wrst/En1+ Lhx1tm1Tmj/Lhx1tm2.1Bhr Lhx5tm1Lmgd/Lhx5tm1Lmgd involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ	absent Purkinje cell layer	J:123471
	decreased Purkinje cell number	J:123471
	small cerebellum	J:123471
Lhx1tm1Bhr/Lhx1+ Pgap1oto/Pgap1+ involves: 129S7/SvEvBrd * C57BL/6J * STOCK In(1)1Rk/J	abnormal telencephalon morphology	J:41878
Lhx1tm1Bhr/Lhx1+ Pgap1oto/Pgap1oto involves: 129S7/SvEvBrd * C57BL/6J * STOCK In(1)1Rk/J	abnormal brain morphology	J:41878
	abnormal diencephalon morphology	J:41878
	abnormal telencephalon morphology	J:41878
Lhx1tm1Bhr/Lhx1+ Ssbp3Tg(SOD1)1Hssk/Ssbp3+ involves: 129S7/SvEvBrd * C3H/He * C57BL/6 * ICR	embryonic growth retardation	J:98485
	failure of initiation of embryo turning	J:98485
	microcephaly	J:98485
Lhx1tm1Bhr/Lhx1tm1Bhr Pgap1oto/Pgap1+ involves: 129S7/SvEvBrd * C57BL/6J * STOCK In(1)1Rk/J	abnormal brain morphology	J:41878
	abnormal developmental patterning	J:41878
Lhx1tm1Tmj/Lhx1+ Rettm1Kln/Rettm1Kln Tg(Nes-cre)1Kln/0 involves: 129/Sv * BALB/c * C57BL/6 * CBA/J * SJL	abnormal axon guidance	J:110955
Lhx1tm1Tmj/Lhx1+ Rettm1.1Kln/Rettm1.1Kln involves: 129/Sv * BALB/c * C57BL/6 * CBA/J	abnormal axon guidance	J:110955
Lhx1tm1Tmj/Lhx1tm4Bhr Lhx5tm1Lmgd/Lhx5tm1Lmgd Tg(Nes-cre)1Kln/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	absent cerebellar foliation	J:123471
	absent Purkinje cell layer	J:123471
	decreased Purkinje cell number	J:123471
	small cerebellum	J:123471