60 phenotypes from 2 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fbln1Gt(XST011)Byg/Fbln1Gt(XST011)Byg B6.129P2-Fbln1Gt(XST011)Byg	atrial septal defect	J:137690
	overriding aortic valve	J:137690
	ventricular septal defect	J:137690
Fbln1Gt(XST011)Byg/Fbln1Gt(XST011)Byg involves: 129P2/OlaHsd * C57BL/6	aberrant origin of the right subclavian artery	J:137690
	abnormal blood vessel morphology	J:137690
	abnormal cardiovascular system morphology	J:137690
	abnormal common carotid artery morphology	J:137690
	abnormal cranial nerve morphology	J:137690
	abnormal cranium morphology	J:137690
	abnormal frontal bone morphology	J:137690
	abnormal glossopharyngeal nerve morphology	J:137690
	abnormal heart morphology	J:137690
	abnormal nasal bone morphology	J:137690
	abnormal otic vesicle development	J:137690
	abnormal parietal bone morphology	J:137690
	abnormal premaxilla morphology	J:137690
	abnormal pulmonary alveolus morphology	J:137690
	abnormal rhombomere morphology	J:137690
	abnormal truncus arteriosus septation	J:137690
	abnormal tympanic ring morphology	J:137690
	abnormal vagus nerve morphology	J:137690
	atrial septal defect	J:137690
	double outlet right ventricle	J:137690
	eye hemorrhage	J:137690
	fusion of glossopharyngeal and vagus nerve	J:137690
	hemorrhage	J:137690
	increased hindbrain apoptosis	J:137690
	internal hemorrhage	J:137690
	intracerebral hemorrhage	J:137690
	micrognathia	J:137690
	muscular ventricular septal defect	J:137690
	neonatal lethality, complete penetrance	J:137690
	ostium primum atrial septal defect	J:137690
	ostium secundum atrial septal defect	J:137690
	overriding aortic valve	J:137690
	perimembraneous ventricular septal defect	J:137690
	petechiae	J:137690
	respiratory distress	J:137690
	retroesophageal right subclavian artery	J:137690
	small lung	J:137690
	small thyroid cartilage	J:137690
	spinal hemorrhage	J:137690
	thymus hypoplasia	J:137690
	thyroid gland hypoplasia	J:137690
	ventricle myocardium hypoplasia	J:137690
	ventricular septal defect	J:137690
Fbln1Gt(XST011)Byg/Fbln1tm1Tmpl involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	atrial septal defect	J:137690
	double outlet right ventricle	J:137690
	overriding aortic valve	J:137690
	ventricular septal defect	J:137690
Fbln1tm1Tmpl/Fbln1tm1Tmpl involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal breathing pattern	J:71581
	abnormal capillary morphology	J:71581
	abnormal glomerular capillary endothelium morphology	J:71581
	abnormal lung development	J:71581
	abnormal lung interstitium morphology	J:71581
	abnormal podocyte foot process morphology	J:71581
	abnormal renal glomerulus morphology	J:71581
	atrial septal defect	J:137690
	decreased body size	J:71581
	decreased body weight	J:71581
	decreased glomerular capillary number	J:71581
	decreased hematocrit	J:71581
	dilated glomerular capillary	J:71581
	double outlet right ventricle	J:137690
	hemorrhage	J:71581
	impaired lung alveolus development	J:71581
	intracranial hemorrhage	J:71581
	overexpanded pulmonary alveolus	J:71581
	perinatal lethality, incomplete penetrance	J:71581
	petechiae	J:71581
	postnatal lethality, incomplete penetrance	J:71581
	thymus hypoplasia	J:137690
	ventricular septal defect	J:137690