43 phenotypes from 4 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Foxd3tm1.1Lby/Foxd3tm1.1Lby either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * CD-1)	abnormal cell proliferation	J:79491
	abnormal developmental patterning	J:79491
	abnormal embryonic epiblast morphology	J:79491
	abnormal extraembryonic endoderm formation	J:79491
	abnormal proximal-distal axis patterning	J:79491
	failure of primitive streak formation	J:79491
	failure to gastrulate	J:79491
	prenatal lethality, complete penetrance	J:79491
Foxd3tm1Lby/Foxd3tm1Lby either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * CD-1)	abnormal anterior visceral endoderm cell migration	J:79491
	abnormal cell proliferation	J:79491
	abnormal developmental patterning	J:79491
	abnormal embryonic epiblast morphology	J:79491
	abnormal extraembryonic endoderm formation	J:79491
	abnormal proximal-distal axis patterning	J:79491
	absent mesoderm	J:79491
	decreased embryonic epiblast cell proliferation	J:79491
	embryonic lethality, complete penetrance	J:79491
	failure of primitive streak formation	J:79491
	failure to gastrulate	J:79491
	small embryonic epiblast	J:79491
Foxd3tm1Lby/Foxd3tm1Lby involves: 129S6/SvEvTac * CD-1	abnormal placenta labyrinth morphology	J:101652
	abnormal trophoblast layer morphology	J:101652
	absent spongiotrophoblast	J:101652
Foxd3tm2Lby/Foxd3tm2Lby involves: 129S6/SvEvTac	abnormal cell proliferation	J:79491
	abnormal developmental patterning	J:79491
	abnormal embryonic epiblast morphology	J:79491
	abnormal extraembryonic endoderm formation	J:79491
	abnormal proximal-distal axis patterning	J:79491
	embryonic lethality, complete penetrance	J:79491
	failure of primitive streak formation	J:79491
	failure to gastrulate	J:79491
Foxd3tm2Lby/Foxd3tm2Lby involves: 129S6/SvEvTac * CD-1	abnormal placenta labyrinth morphology	J:101652
	abnormal trophoblast layer morphology	J:101652
	absent spongiotrophoblast	J:101652
Foxd3tm2Lby/Foxd3tm3Lby H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S6/SvEvTac * C57BL/6 * CBA	abnormal cardiac neural crest cell migration	J:134482
	abnormal common carotid artery morphology	J:134482
	abnormal cranium morphology	J:134482
	abnormal dorsal spinal root morphology	J:134482
	abnormal enteric nervous system morphology	J:134482
	abnormal enteric neural crest cell migration	J:134482
	abnormal heart development	J:134482
	abnormal spinal nerve morphology	J:134482
	absent frontal bone	J:134482
	absent nasal capsule	J:134482
	cleft palate	J:134482
	eyelids open at birth	J:134482
	increased apoptosis	J:134482
	increased hindbrain apoptosis	J:134482
	mandibular hyperostosis	J:134482
	midline facial cleft	J:134482
	perinatal lethality, complete penetrance	J:134482
	persistent truncus arteriosus	J:134482
	respiratory failure	J:134482
	short mandible	J:134482
	short maxilla	J:134482
	short premaxilla	J:134482
	small basioccipital bone	J:134482
	small dorsal root ganglion	J:134482
	small interparietal bone	J:134482
	small parietal bone	J:134482
	small pharyngeal arch	J:134482