16 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Fgf3tm1Lwd/Fgf3tm1Lwd Fgf4tm1.1Lwd/Fgf4tm1.1Lwd involves: 129S4/SvJae * C57BL/6 * C57BL/6 * NIH Swiss Webster * SJL/J	abnormal presomitic mesoderm morphology	J:229949
	circling	J:229949
	decreased body size	J:229949
	head tilt	J:229949
	short tail	J:229949
Fgf3tm1Lwd/Fgf3tm1Lwd Fgf4tm1.1Lwd/Fgf4tm1.2Lwd involves: 129S4/SvJae * C3H * C57BL/6 * C57BL/6 * NIH Swiss Webster * SJL/J	abnormal presomitic mesoderm morphology	J:229949
	decreased caudal vertebrae number	J:229949
	short rostral-caudal axis	J:229949
Fgf8tm1.3Mrt/Fgf8tm1.4Mrt Tg(CAG-Bgeo,-Fgf4)1Mrt/? Tg(Msx2-cre)5Rem/? involves: 129P2/OlaHsd	abnormal digit development	J:104411
	abnormal eyelid morphology	J:104411
	abnormal limb bud morphology	J:104411
	abnormal limb development	J:104411
	abnormal reproductive system morphology	J:104411
	fused tarsal bones	J:104411
	normal limbs/digits/tail phenotype	J:104411
	polysyndactyly	J:104411
	postnatal growth retardation	J:104411