29 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Pdgfatm1Cbet/Pdgfa+ Pdgfctm1Nagy/Pdgfctm1Nagy involves: 129S1/Sv * 129X1/SvJ * C57BL/6	spina bifida	J:205009
Pdgfatm1Cbet/Pdgfatm1Cbet Pdgfctm1Nagy/Pdgfctm1Nagy involves: 129S1/Sv * 129X1/SvJ	abnormal axial skeleton morphology	J:93954
	abnormal craniofacial bone morphology	J:93954
	abnormal kidney cortex morphology	J:93954
	abnormal myotome development	J:93954
	abnormal scapula morphology	J:93954
	abnormal somite development	J:93954
	blistering	J:93954
	common atrium	J:93954
	decreased embryo size	J:93954
	embryonic lethality during organogenesis, complete penetrance	J:93954
	hydrops fetalis	J:93954
	midline facial cleft	J:93954
	pericardial effusion	J:93954
	rib bifurcation	J:93954
	rib fusion	J:93954
	short sternum	J:93954
	spina bifida	J:93954
	wavy neural tube	J:93954
Pdgfatm1Cbet/Pdgfatm2Cbet Pdgfratm11(EGFP)Sor/Pdgfra+ involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6	abnormal lung morphology	J:205009
	abnormal pulmonary alveolus morphology	J:205009
	normal digestive/alimentary phenotype	J:205009
	emphysema	J:205009
	normal renal/urinary system phenotype	J:205009
	normal skeleton phenotype	J:205009
Pdgfatm2Cbet/Pdgfatm2Cbet Pdgfctm1Nagy/Pdgfctm1Nagy B6.129-Pdgfctm1Nagy Pdgfatm2Cbet	spina bifida	J:205009
	spina bifida occulta	J:205009
Pdgfatm2Cbet/Pdgfatm2Cbet Pdgfctm1Nagy/Pdgfctm1Nagy involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal small intestine morphology	J:205009
	decreased body size	J:205009
	decreased small intestinal villus number	J:205009
	kyphosis	J:205009
	spina bifida	J:205009
	spina bifida occulta	J:205009