50 phenotypes from 6 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ltbp1b2b1000Clo/Ltbp1b2b1000Clo C57BL/6J-Ltbp1b2b1000Clo	dilated renal tubule	J:175213
	double outlet right ventricle	J:175213
	interrupted aortic arch	J:175213
	persistent truncus arteriosus	J:175213
	polycystic kidney	J:175213
	renal glomerulus cyst	J:175213
	right aortic arch	J:175213
	vascular ring	J:175213
Ltbp1tm1a(EUCOMM)Wtsi/Ltbp1+ B6JTyr;B6N-Ltbp1tm1a(EUCOMM)Wtsi/Wtsi	increased leukocyte cell number	J:175295
Ltbp1tm1a(EUCOMM)Wtsi/Ltbp1tm1a(EUCOMM)Wtsi B6JTyr;B6N-Ltbp1tm1a(EUCOMM)Wtsi/Wtsi	abnormal cranium morphology	J:175295
	abnormal incisor morphology	J:175295
	abnormal radius morphology	J:175295
	abnormal snout morphology	J:175295
	abnormal tooth morphology	J:175295
	abnormal ulna morphology	J:175295
	decreased body length	J:175295
	decreased body weight	J:175295
	decreased bone mineral content	J:175295
	decreased circulating alanine transaminase level	J:175295
	decreased circulating aspartate transaminase level	J:175295
	decreased circulating cholesterol level	J:175295
	decreased circulating HDL cholesterol level	J:175295
	decreased circulating iron level	J:175295
	decreased circulating LDL cholesterol level	J:175295
	decreased circulating serum albumin level	J:175295
	decreased circulating total protein level	J:175295
	decreased total body fat amount	J:175295
	increased blood urea nitrogen level	J:175295
	increased hemoglobin content	J:175295
	increased mean corpuscular hemoglobin	J:175295
Ltbp1tm1Rawe/Ltbp1tm1Rawe B6.129X1-Ltbp1tm1Rawe	abnormal cranium morphology	J:133255
	abnormal jaw morphology	J:133255
	abnormal lower incisor morphology	J:133255
	liver fibrosis	J:133255
	short mandible	J:133255
	short maxilla	J:133255
	short snout	J:133255
	small basioccipital bone	J:133255
	small basisphenoid bone	J:133255
Ltbp1tm1Veto/Ltbp1tm1Veto involves: 129 * C57BL/6	abnormal cardiac neural crest cell morphology	J:128012
	abnormal coronary artery morphology	J:128012
	abnormal fourth pharyngeal arch artery morphology	J:128012
	abnormal truncus arteriosus septation	J:128012
	abnormal vascular smooth muscle morphology	J:128012
	common atrium	J:128012
	cyanosis	J:128012
	interrupted aortic arch	J:128012
	lethality throughout fetal growth and development, incomplete penetrance	J:128012
	neonatal lethality, complete penetrance	J:128012
	perimembraneous ventricular septal defect	J:128012
	persistent truncus arteriosus	J:128012
	right aortic arch	J:128012
Ltbp1tm1Vlcg/Ltbp1tm1Vlcg involves: 129S/SvEv * C57BL/6 * FVB/N	normal integument phenotype	J:228706
Ltbp1tm2Veto/Ltbp1tm2Veto involves: 129 * C57BL/6	abnormal ascending aorta and coronary artery attachment	J:128012
	abnormal cardiac neural crest cell morphology	J:128012
	abnormal fourth pharyngeal arch artery morphology	J:128012
	abnormal truncus arteriosus septation	J:128012
	abnormal vascular smooth muscle morphology	J:128012
	common atrium	J:128012
	cyanosis	J:128012
	interrupted aortic arch	J:128012
	lethality throughout fetal growth and development, incomplete penetrance	J:128012
	neonatal lethality, complete penetrance	J:128012
	perimembraneous ventricular septal defect	J:128012
	persistent truncus arteriosus	J:128012
	right aortic arch	J:128012