43 phenotypes from 2 alleles in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Wdr19dmhd/Wdr19dmhd involves: FVB/NJ	abnormal cilium morphology	J:181888
	abnormal limb paddle morphology	J:181888
	embryonic lethality during organogenesis, complete penetrance	J:181888
Wdr19dmhd/Wdr19twto involves: FVB/NJ	abnormal limb paddle morphology	J:181888
	lethality throughout fetal growth and development, complete penetrance	J:181888
Wdr19twto/Wdr19twto involves: FVB/NJ	abnormal cilium morphology	J:181888
	abnormal craniofacial development	J:181888
	abnormal cranium morphology	J:181888
	abnormal dermomyotome development	J:181888
	abnormal limb development	J:181888
	abnormal limb mesenchyme morphology	J:181888
	abnormal limb paddle morphology	J:181888
	abnormal mandibular angle morphology	J:181888
	abnormal maxilla morphology	J:181888
	abnormal myotome development	J:181888
	abnormal palatal shelf fusion at midline	J:181888
	abnormal palatine bone morphology	J:181888
	abnormal premaxilla morphology	J:181888
	abnormal rib morphology	J:181888
	abnormal somite development	J:181888
	abnormal spine curvature	J:181888
	abnormal sternum ossification	J:181888
	abnormal tympanic ring morphology	J:181888
	abnormal vertebrae morphology	J:181888
	absent frontal bone	J:181888
	absent supraoccipital bone	J:181888
	absent tibia	J:181888
	anophthalmia	J:181888
	bilateral cleft upper lip	J:181888
	cleft palate	J:181888
	cleft secondary palate	J:181888
	decreased palatine bone horizontal plate size	J:181888
	ectopic digits	J:181888
	exencephaly	J:181888
	interparietal bone hypoplasia	J:181888
	lethality throughout fetal growth and development, complete penetrance	J:181888
	parietal bone hypoplasia	J:181888
	polydactyly	J:181888
	polyphalangy	J:181888
	rib bifurcation	J:181888
	rib fusion	J:181888
	short face	J:181888
	short mandible	J:181888
	short maxilla	J:181888
	short premaxilla	J:181888
	short ribs	J:181888
	split sternum	J:181888