29 phenotypes from 2 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pdgfatm1Cbet/Pdgfatm1Cbet involves: 129P2/OlaHsd * C57BL	abnormal lung morphology	J:33629
	abnormal pulmonary alveolar parenchyma morphology	J:33629
	abnormal pulmonary elastic fiber morphology	J:33629
	abnormal pulmonary interalveolar septum morphology	J:33629
	absent pulmonary alveoli	J:33629
	atelectasis	J:33629
	decreased body size	J:33629
	decreased fetal size	J:33629
	embryonic lethality during organogenesis, incomplete penetrance	J:33629
	emphysema	J:33629
	enlarged thoracic cavity	J:33629
	fetal growth retardation	J:33629
	heart right ventricle hypertrophy	J:33629
	impaired lung alveolus development	J:33629
	lung hemorrhage	J:33629
	pneumothorax	J:33629
	postnatal growth retardation	J:33629
	postnatal lethality, incomplete penetrance	J:33629
	premature death	J:33629
	thick ventricular wall	J:33629
Pdgfatm1Cbet/Pdgfatm1Cbet involves: 129P2/OlaHsd * C57BL/6	abnormal epididymis epithelium morphology	J:89838
	abnormal epididymis morphology	J:89838
	abnormal spermatogenesis	J:89838
	arrest of spermatogenesis	J:89838
	postnatal lethality, incomplete penetrance	J:89838
	respiratory failure	J:89838
Pdgfatm1Cbet/Pdgfatm1Cbet involves: 129S1/Sv * 129X1/SvJ	abnormal small intestine morphology	J:205009
	decreased small intestinal villus number	J:205009
Pdgfatm2Cbet/Pdgfatm2Cbet involves: 129S1/Sv * 129X1/SvJ * C57BL/6	normal mortality/aging	J:205009
	normal respiratory system phenotype	J:205009