31 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Ldb1tm1Lmgd/Ldb1+ Ssbp3Tg(SOD1)1Hssk/Ssbp3+ involves: C3H/He * C57BL/6	embryonic growth retardation	J:98485
	microcephaly	J:98485
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
Ssbp3Tg(SOD1)1Hssk/Ssbp3+ involves: 129S7/SvEvBrd * C3H/He * C57BL/6 * ICR	no abnormal phenotype detected	J:98485
Ssbp3Tg(SOD1)1Hssk/Ssbp3+ involves: C3H/He * C57BL/6	no abnormal phenotype detected	J:98485
Ssbp3Tg(SOD1)1Hssk/Ssbp3Tg(SOD1)1Hssk involves: C3H/He * C57BL/6	abnormal anterior head development	J:98485
	abnormal brain development	J:98485
	abnormal cephalic neural fold morphology	J:98485
	abnormal cranium morphology	J:98485
	abnormal forebrain development	J:98485
	abnormal midbrain development	J:98485
	abnormal midbrain-hindbrain boundary development	J:98485
	abnormal neural plate morphology	J:98485
	abnormal somite development	J:98485
	abnormal somite shape	J:98485
	abnormal sternum morphology	J:98485
	abnormal telencephalon development	J:98485
	abnormal vertebral body morphology	J:98485
	absent diencephalon	J:98485
	absent prechordal plate	J:98485
	asymmetric sternocostal joints	J:98485
	decreased cell proliferation	J:98485
	decreased embryo size	J:98485
	decreased somite size	J:98485
	decreased sternebra number	J:98485
	embryonic lethality during organogenesis, incomplete penetrance	J:98485
	increased apoptosis	J:98485
	kinked neural tube	J:98485
	lethality throughout fetal growth and development, incomplete penetrance	J:98485
	microcephaly	J:98485
	rib bifurcation	J:98485
	rib fusion	J:98485
	short tail	J:98485