37 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Alx1tm1Crm/Alx1tm1Crm Alx3tm1Hubr/Alx3tm1Hubr involves: 129P2/OlaHsd * 129S7/SvEvBrd	abnormal scapula morphology	J:101708
Alx3tm1Hubr/Alx3tm1Hubr Alx4lst-J/Alx4lst-J involves: 129P2/OlaHsd * C3H * C57BL/6J * FVB/N	abnormal basicranium morphology	J:71880
	abnormal clavicle morphology	J:71880
	abnormal craniofacial bone morphology	J:71880
	abnormal cranium morphology	J:71880
	abnormal mandible morphology	J:71880
	abnormal maxilla morphology	J:71880
	abnormal maxillary frontal process morphology	J:71880
	abnormal nasal capsule morphology	J:71880
	abnormal nasal cavity morphology	J:71880
	abnormal neurocranium morphology	J:71880
	abnormal premaxilla morphology	J:71880
	abnormal pterygoid process morphology	J:71880
	abnormal viscerocranium morphology	J:71880
	absent deltoid tuberosity	J:71880
	absent facial bone	J:71880
	absent gastric milk in neonates	J:71880
	absent nasal septum	J:71880
	bifid nasal tip	J:71880
	bifid nose	J:71880
	cleft palate	J:71880
	decreased cranium height	J:71880
	exophthalmos	J:71880
	eyelids open at birth	J:71880
	increased cranium width	J:71880
	large fontanelles	J:71880
	meteorism	J:71880
	midline facial cleft	J:71880
	neonatal lethality, complete penetrance	J:71880
	preaxial polydactyly	J:71880
	short facial bone	J:71880
	short temporal bone squamous part	J:71880
	small alisphenoid bone	J:71880
	small frontal bone	J:71880
	small nasal bone	J:71880
	small parietal bone	J:71880
Alx3tm1Hubr/Alx3tm1Hubr Alx4lst-J/Alx4lst-J involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J	small pubis	J:101708